SlideShare a Scribd company logo
1 of 12
Download to read offline
Dun et al. Cardiovasc Diabetol (2019) 18:104
https://doi.org/10.1186/s12933-019-0907-0
ORIGINAL INVESTIGATION
High‑intensity interval training improves
metabolic syndrome and body composition
in outpatient cardiac rehabilitation patients
with myocardial infarction
Yaoshan Dun1,2
, Randal J. Thomas2
, Joshua R. Smith2
, Jose R. Medina‑Inojosa2
, Ray W. Squires2
,
Amanda R. Bonikowske2
, Hsuhang Huang2
, Suixin Liu1*
and Thomas P. Olson2*
Abstract 
Background:  To examine the effect of high-intensity interval training (HIIT) on metabolic syndrome (MetS) and body
composition in cardiac rehabilitation (CR) patients with myocardial infarction (MI).
Methods:  We retrospectively screened 174 consecutive patients with MetS enrolled in CR following MI between
2015 and 2018. We included 56 patients who completed 36 CR sessions and pre-post dual-energy X-ray absorptiom‑
etry. Of these patients, 42 engaged in HIIT and 14 in moderate-intensity continuous training (MICT). HIIT included
4–8 intervals of high-intensity (30–60 s at RPE 15–17 [Borg 6–20]) and low-intensity (1–5 min at RPE < 14), and MICT
included 20–45 min of exercise at RPE 12–14. MetS and body composition variables were compared between MICT
and HIIT groups.
Results:  Compared to MICT, HIIT demonstrated greater reductions in MetS (relative risk = 0.5, 95% CI 0.33–0.75,
P < .001), MetS z-score (− 3.6 ± 2.9 vs. − 0.8 ± 3.8, P < .001) and improved MetS components: waist circumference
(− 3 ± 5 vs. 1 ± 5 cm, P = .01), fasting blood glucose (− 25.8 ± 34.8 vs. − 3.9 ± 25.8 mg/dl, P < .001), triglycerides
(− 67.8 ± 86.7 vs. − 10.4 ± 105.3 mg/dl, P < .001), and diastolic blood pressure (− 7 ± 11 vs. 0 ± 13 mmHg, P = .001).
HIIT group demonstrated greater reductions in body fat mass (− 2.1 ± 2.1 vs. 0 ± 2.2 kg, P = .002), with increased body
lean mass (0.9 ± 1.9 vs. − 0.9 ± 3.2 kg, P = .01) than the MICT. After matching for exercise energy expenditure, HIIT-
induced improvements persisted for MetS z-score (P < .001), MetS components (P < .05), body fat mass (P = .002), body
fat (P = .01), and lean mass (P = .03).
Conclusions:  Our data suggest that, compared to MICT, supervised HIIT results in greater improvements in MetS and
body composition in MI patients with MetS undergoing CR.
Keywords:  Cardiac rehabilitation, High-intensity interval training, Metabolic syndrome, Myocardial infarction, Body
composition
© The Author(s) 2019. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License
(http://creat​iveco​mmons​.org/licen​ses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium,
provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creat​iveco​mmons​.org/
publi​cdoma​in/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Open Access
Cardiovascular Diabetology
*Correspondence: liusuixin@csu.edu.cn; olson.thomas2@mayo.edu
1
Division of Cardiac Rehabilitation, Department of Physical Medicine
& Rehabilitation, Xiangya Hospital Central South University, 87 Xiangya
Road, Changsha, Hunan, People’s Republic of China
2
Division of Preventive Cardiology, Department of Cardiovascular
Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 2 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
Background
Metabolic syndrome (MetS) is a constellation of cardio-
vascular risk factors that include abdominal adiposity,
impaired glucose tolerance, hypertension, low serum
high-density lipoprotein cholesterol and hypertriglyc-
eridemia [1], and is associated with an eightfold increase
in the risk of myocardial infarction (MI) [2]. Presence of
MetS in patients with MI is associated with increased risk
of adverse cardiovascular events and recurrent MI [3].
Obesity, especially abdominal adiposity is also consid-
ered an initial and principal pathophysiologic component
of MetS [4]. More effective interventions to ameliorate
MetS and reduce body fat among survivors of MI are
critical to improving MI outcomes.
Current guidelines recommend exercise training as
adjunctive therapy in patients with MI [5]. Exercise train-
ing improves body composition, cardiovascular, and
metabolic outcomes in people with MetS [6]. High vol-
ume of physical activity is associated with lower rates
of CVD events, glycosylated hemoglobin (HbA1C %),
and systolic blood pressure in older adults [7]. However,
universal agreement on the most effective exercise pre-
scription to improve MetS for patients with MI remains
unclear. Recent studies have demonstrated that high-
intensity interval training (HIIT) may ameliorate MetS
in obese adults [8], optimize HbA1C in patients with
type II diabetes [9], and improve cardiac function in MI
patients [10], more so than moderate-intensity continu-
ous training (MICT) [8, 10]. However, the impact of HIIT
on MetS in patients with MI undergoing early outpatient
cardiac rehabilitation (CR) has not been studied.
The purpose of this study was to examine the effect
of supervised HIIT on MetS presence and severity, and
body composition in patients with MI undergoing early
outpatient CR. We hypothesized that HIIT will be associ-
ated with greater improvements in MetS and body com-
position compared to MICT.
Methods
Design and participants
This was a retrospective cohort study of 391 consecutive
MI patients enrolled in early outpatient cardiac reha-
bilitation (CR) at Mayo Clinic, Rochester, MN between
September 1st, 2015 and February 28th, 2018. Of 391
patients, 174 MI patients presented with MetS. Patients
meeting the following inclusion criteria were included:
(1) diagnosed with both MI and MetS, (2) completion of
36 sessions of supervised outpatient cardiac rehabilita-
tion, (3) pre- and post-CR blood lipids and fasting blood
glucose tests, and (4) completed pre- and post-CR dual
energy X-ray absorptiometry. The cardiac rehabilitation
program at Mayo Clinic is a multidisciplinary health
care program that includes a highly supervised exercise
program (36 exercise sessions), patient education and
wellness programs, nutrition and smoking cessation
counseling, stress management, and psychological and
pharmacological counseling. A standard 36 sessions of
CR usually lasts 12 weeks (three sessions per week). Of
the 56 eligible patients who met all the inclusion criteria,
42 engaged in HIIT and 14 in MICT (Fig. 1). All aspects
of this study conformed to the principles outlined in the
Declaration of Helsinki and were approved by the Mayo
Clinic Institutional Review Board. All participants agreed
to use of their medical records for research purposes.
HIIT and MICT protocols
Patients performed an average of three supervised HIIT
or MICT sessions/week on a treadmill, cycle ergom-
eter, or recumbent stepper in the CR center and were
prescribed 3  days of self-guided exercise at home. In
the 1st week, all patients performed MICT, after that,
if patients were able to exercise for ≥ 
20 min at a rat-
ing of perceived exertion (RPE: Borg 6–20) of 12–14,
they self-determined to continue MICT or transition
to HIIT. The HIIT sessions were characterized by brief,
intermittent bouts of high-intensity exercise inter-
spersed with periods of low-intensity exercise (active
recovery). Because most patients are prescribed heart
rate modulating pharmacotherapy after MI and to
maximize generalizability and real-world applicability,
the intensity of HIIT was prescribed using RPE. These
patients began with four high-intensity intervals of
30–60 s at an RPE of 15–17 interspersed with 1–5 min
of low-intensity intervals at an RPE 
< 
14, progress-
ing to 5–8 high-intensity intervals of 2–4  min during
20–45 min of training according to the American Col-
lege of Sports Medicine (ACSM) guidelines [11]. HIIT
was performed only during supervised sessions with
frequency not exceeding 3 days/week (non-consecutive
days). MICT was performed for 20–45 min at an RPE
of 12–14. Heart rate (HR) and rhythm were continu-
ously monitored via a 3-lead electrocardiogram (Q-Tel
telemonitoring system, Welch Allyn, USA) with blood
pressure (systolic [SBP] and diastolic [DBP]) meas-
ured by manual sphygmomanometry. Heart rate (HR)
data were retrieved from the exercise session report of
each patient, which provided documentation on HRs
at specific time-points including: (a) before and after
each exercise training session for both HIIT and MICT
groups, (b) at the end of the second and third intervals
for HIIT, and (c) at the mid-point and end of exercise
for MICT. Average HR was calculated by averaging
HR values that were documented during exercise. The
average metabolic equivalent (MET) and exercise time
for each exercise session were reported by the Q-Tel
telemonitoring system and documented in exercise
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 3 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
session reports. Energy expenditure (EE) was calculated
according to the equation: calories 
= [METs × body
weight in kilograms 
× 3.5]/200 × 
exercise time, as
described previously [12].
Metabolic syndrome criteria
The definition of metabolic syndrome (MetS) is based
on the revised National Cholesterol Education Program’s
Adult Treatment Panel III (ATP III) [1]. An ATP III MetS
score was calculated as the sum of the ATP III MetS cri-
teria at baseline and completion of CR.
Metabolic syndrome z‑score
Metabolic syndrome z-score is a continuous score of each
MetS variable defined by ATP III, and was calculated
from modified z-scores of the following variables: [13]
waist circumference; SBP; DBP; triglycerides (TG); fast-
ing blood glucose (FBG); ATP III criteria, and standard
deviations (denominator of each factor in the formula)
using baseline data from the entire study cohort (N = 56):
Metabolic syndrome z-score 
= [(50-HDL)/9.9] + [(TG-
150)/69.8] + [(FBG-100)/24.5] + [(WC-88)/10.3] + [(SBP-
130)/16.0] + [(DBP-85)/11.2].
Anthropometric measurement
Dual-energy X-ray absorptiometry (Lunar iDXA Series
X, Madison, WI, USA) was conducted by trained radi-
ology technicians using standardized procedures as
described previously [14]. The scans were performed
within 1 week prior to starting and 1 week after comple-
tion of CR. Scans were used to measure total body mass,
body fat mass, body lean mass, body fat percentage, and
abdominal region fat percentage (the area between the
ribs and pelvis). Percentages of the total were calculated
accordingly. The scanner was calibrated daily against
a manufacturer supplied standard calibration block to
control for possible baseline drift. Height was measured
using a stadiometer.
Dietary assessment
Dietary assessment was performed using the Rate-Your-
Plate (RYP) questionnaire as previously described [15]
during the first and last CR session.
Statin therapy intensity assessment
Due to the known influence of statin therapy on blood
lipids and body composition, we retrieved and analyzed
statin therapy intensity data for each patient. Statin
Fig. 1  Study enrollment. HIIT high-intensity interval training, MICT moderate-intensity continuous training, DXA dual-energy X-ray absorptiometry
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 4 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
therapy intensity was assessed within 1 week prior to the
start and within 1 week after the completion of CR and
stratified using ACC/AHA guidelines [16]. Statin inten-
sity therapy is defined as a pseudo-continuous variable,
3 = 
high intensity, 2 
= 
moderate intensity, 1 
= low inten-
sity, and 0 = none.
Exercise capacity
Exercise capacity was evaluated at the beginning and
completion of 36 sessions of CR via standard exer-
cise stress test, cardiopulmonary exercise test (CPET)
or 6 min walk test (6 MWT). The protocols of pre- and
post-intervention were the same for each patient. In
the present study, exercise capacity was represented
as peak oxygen consumed ­
(VO2peak, ml/kg/min) that
was directly measured by performing CPET (HIIT 
= 28;
MICT = 
9), the ­
VO2peak calculated by the equation
­VO2peak = 3.5  ml/kg/min * peak metabolic equivalents
(METs) that was determined by standard exercise stress
test (HIIT 
= 8; MICT = 
3), or the ­
VO2peak calculated
from the equation ­
VO2peak = 4.9486 + 0.023 * walk dis-
tance (meters) that was determined via using 6 MWT
(HIIT = 6; MICT = 2) as described previously [17].
Depressive symptoms assessment
To determine if there was a difference in HIIT- and
MICT-induced psychological response, we retrieved
Patient Health Questionnaire 9 (PHQ-9) data that was
collected monthly for patients to assess patient’s depres-
sive symptoms. The PHQ-9 test was conducted as
described previously [18].
Statistical analysis
The primary outcomes of this study were the mean dif-
ferences in metabolic syndrome variables from baseline
through 36 sessions of CR between groups. A second-
ary outcome of interest was the mean difference in body
composition, including total body fat mass, body fat per-
centage, abdominal fat percentage, and body lean mass
between groups.
Baseline data are presented as frequency and percent-
age for categorical variables and compared between
groups using the Pearson Chi-square test or Fisher exact
test. Continuous data are presented as mean and stand-
ard deviation and compared between groups using two-
sample t-test or non-parametric Wilcoxon rank-sum
test, as appropriate depending on the distribution. Prior
to analyses, normality was evaluated and the distribu-
tion of changes looked approximately normal. Analysis of
covariance (ANCOVA) was used to compare the change
in each parameter of interest between groups. In this
analysis, change was modeled as the outcome in a lin-
ear regression model and group effects were tested with
adjustment for the baseline value of the parameter being
tested. These analyses were repeated in a matched sub-
set of each group to control for potential differences in
exercise duration, exercise intensity, and exercise energy
expenditure. In order to assess differences over time
between groups, a repeated measures analysis of variance
(ANOVA) was used. In this analysis, measurements at
each week were used to examine the interaction of time
and group and tested the differences in effects over time
between groups. Energy expenditure and METs were log
transformed in these analyses to approximate normality
prior to analysis. Means and confidence intervals were
back-transformed to the original scale for presentation.
Comparisons at each week used the method of Scheffe to
adjust P-values for multiple comparisons. SAS version 9.4
(Cary, NC) was used for analyses and Two-sided P-val-
ues ≤ .05 were considered to be statistically significant.
Results
Study patients
Baseline characteristics were not different between
groups (Table 1): age (69 
± 
14 vs. 68 
± 10 years P = .78),
female (36% vs. 36%, P > .99), body weight (91.2 ± 14.4 vs.
91.5 ± 16.3  kg P = 
.95), height (170 
± 
10 vs. 171 
± 9  cm
P = .84), and BMI (31.5 ± 4.2 vs. 31.3 ± 4.7 kg/m2
P = .90).
Comorbidities and medications were also not different
between groups (P > .05). Percentage of PCI (50% vs. 57%)
and CABG (14% vs. 14%) were not different between
groups (P = .64, P > .99 respectively). Twenty-five patients
suffered one-vessel disease (MICT 
= 
6, 42%; HIIT 
= 17,
40%; P = 
.88), 17 patients suffered two-vessel disease
(MICT = 
4, 29%; HIIT 
= 12, 31%; P = 
.99), 14 patients
suffered three-vessel disease (MICT = 4, 29%; HIIT = 13,
31%; P = 
.74). The number of days between patients’
MI event and the beginning of CR was also not differ-
ent between groups (14 
± 
4 vs. 14 
± 11  days, P = .34).
The ­VO2peak at baseline was not significantly differ-
ent between groups (23.7 
± 
7.1 vs. 23.0 
± 6.3 ml/kg/min,
P = .73).
Exercise parameters over the course of cardiac
rehabilitation
The HIIT group demonstrated significantly higher aver-
age HR, average exercise intensity, longer duration of
exercise, and higher energy expenditure per session at
each time point compared to MICT group (P < .05), while
the average exercise intensity (P = .40), duration of exer-
cise at 12-weeks (P = 
.39), and energy expenditure at
2-weeks (P = .09) and 12-weeks (P = .37) were not differ-
ent between groups. Further, there were no differences
between groups in average HR (P = .81), average exercise
intensity (P = 
.40), duration of exercise (P = .68), energy
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 5 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
expenditure per session (P = .37) across groups over time
(Fig. 2).
Dietary quality and depressive symptoms assessment
The baseline RYP scores in MICT and HIIT were not
different (56 
± 
7 vs. 56 
± 7, P = 
.99). The changes in RYP
scores between groups were not different from base-
line to the completion of 36 CR sessions (5 ± 5 vs. 5 ± 5,
P = .46). The changes in PHQ-9 scores were not different
across the groups after the completion of 36 CR sessions
(− 1.2 ± 3.6 vs. − 1.6 ± 3.5, P = .45).
Statin therapy intensity assessment
All 56 patients were taking statin therapy at baseline. The
changes in average statin therapy intensities between the
groups were not different from baseline to the comple-
tion of 36 CR sessions (0.1 ± 0.3 vs. − 0.1 ± 0.5, P = .30).
Metabolic syndrome
Compared to MICT, the HIIT group demonstrated
greater reductions in MetS presence (relative risk 
= 0.5,
95% confidence interval 0.33–0.75, P < .001), MetS
z-score (− 3.6 ± 2.9 vs. − 0.8 ± 3.8, P < .001), ATP III MetS
scores (P = 
.005) and improvements in individual MetS
variables, including, waist circumference (P = .01), FBG
(P < .001), TG (P = .001) and DBP (P = .001). The changes
in HDL-C and SBP were not different between groups
(Table 2).
Body composition
The HIIT group demonstrated greater improvements
in total body fat mass (P = 
.002), body fat percentage
(P = .002), abdominal fat percentage (P = .004), and body
lean mass (P = .01) compared to MICT (Fig. 3).
Sub‑group analysis
Due to the difference in exercise energy expenditure
between HIIT and MICT, we matched HIIT and MICT
participants for exercise energy expenditure. In this sub-
group analysis, the HIIT group demonstrated greater
improvements in MetS z-score (P < 
.001), ATP III MetS
score (P = 
.005), and MetS variables (including FBG
(P = 
.002), TG (P = 
.008), DBP (P < 
.001), total body fat
mass (P = 
.02), body fat percentage (P = 
.01), body lean
mass (P = 
.03), and abdominal fat percentage (P = .01)
compared to MICT, with no differences in RYP scores
(P = 
.95) and average statin therapy intensity between
groups from baseline to follow-up (P = .23) (Table 3).
Discussion
This study has, for the first time, demonstrated that
supervised HIIT elicited greater improvements in MetS
z-score and ATP III MetS score, and some components
of MetS that include waist circumference, FBG, TG, and
DBP, than MICT in MI patients with MetS enrolled in
early outpatient CR. These findings support the use of
HIIT, as an alternative and/or complimentary to MICT,
for MI patients with MetS to improve CVD risk factor
related outcomes.
Our findings demonstrate that HIIT decreased the
prevalence of MetS and MetS severity (MetS z-score) to a
greater extent than MICT in MI patients enrolled in early
outpatient CR. The observed magnitude of HIIT-induced
benefit in the current study parallels a recent study by
Morales-Palomo et al. [19] in individuals with MetS but
without MI. These authors found that 2 yearly 16-week
HIIT programs resulted in chronically lower MetS and
halted the increase in medication use that occurs in
Table 1  Baseline characteristics of study patients
ACEIs angiotensin-converting enzyme inhibitors, ARBs angiotensin II receptor
blockers, BMI body mass index, CABG coronary artery bypass graft, CCBs calcium
channel blockers, HIIT high-intensity interval training, MICT moderate-intensity
continuous training, PCI percutaneous coronary intervention, VO2peak peak
oxygen consumed
MICT (n = 14) HIIT (n = 42) P value
Age, mean (SD), years 69 ± 14 68 ± 10 P = .78
Female sex, n (%) 5 (36) 15 (36) P > .99
Height, mean (SD), cm 170 ± 10 171 ± 9 P = .84
Body weight, mean (SD), kg 91.2 ± 14.4 91.5 ± 16.3 P = .95
BMI, mean (SD), kg/m2
31.5 ± 4.2 31.3 ± 4.7 P = .90
Days between CR and MI,
mean (SD), days
14 ± 4 14 ± 11 P = .34
Medical history, n (%)
 PCI 7 (50) 24 (57) P = .64
 CABG 2 (14) 6 (14) P > .99
 Hyperglycemia 11 (79) 33 (79) P > .99
 Hypertension 8 (57) 20 (48) P = .54
 Dyslipidemia 14 (100) 39 (92) P = .57
 Ever smoker 5 (36) 14 (33) P > .99
Coronary angiography
 One-vessel disease, n (%) 6 (42) 17 (40) P = .88
 Two-vessel disease, n (%) 4 (29) 12 (29) P = .99
 Three-vessel disease, n (%) 4 (29) 13 (31) P = .74
Medications, n (%)
 Insulin 3 (21) 9 (21) P > .99
 Oral hypoglycemic drugs 4 (29) 15 (36) P = .75
 Statins 14 (100) 42 (100) P = .99
 ACEIs/ARBs 9 (64) 24 (57) P = .64
 Antiplatelet drugs 12 (86) 41 (98) P = .15
 Anticoagulants 7 (50) 26 (62) P = .43
 Beta receptor blockers 9 (64) 37 (88) P = .10
 CCBs 2 (14) 7 (17) P > .99
 Diuretics 2 (14) 1 (2) P = .15
 Nitrates 4 (29) 6 (14) P = .25
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 6 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
non-exercising MetS individuals. Similarly, Ramos et al.
[8] demonstrated low-volume HIIT was sufficient to
ameliorate the MetS severity in middle-aged adults, and
was superior to MICT in terms of time efficiency. In
addition, an across race study demonstrated that high-
intensity interval and resistance training led to improve-
ments in cardiometabolic risk factors, including FBG,
TG, and SBP, in both Mapuche and European hyper-
glycemic adult women [20]. Our findings are consistent
with these observations further supporting the important
impact of HIIT on components of MetS and suggest that
HIIT could be encouraged for MI patient with MetS.
The present study, for the first time, demonstrated
that HIIT contributes to greater decreases in total body
fat mass (P = 
.002), body fat percentage (P = .002), and
abdominal fat percentage (P < .004) while increasing body
lean mass (P = 
.01) in MI patients with MetS compared
to MICT. Several other studies have also examined the
efficacy of HIIT on reducing subcutaneous and abdomi-
nal fat in overweight adolescents [21] and type 2 diabetic
men [22]. Trapp et al. [23] compared HIIT and MICT in
young women and found that HIIT resulted in greater
reductions in subcutaneous fat. These are important
findings, as increasing evidence suggests body fat (and
its distribution) and lean body mass are associated with
risk of incident MetS [24, 25]. For example, risk of MetS
for individuals in the highest abdominal fat quintile is
more than three times greater compared with the lowest
quintile [25]. Moreover, individuals with high fat and low
muscle mass have an approximately twofold increase in
the risk of developing MetS [24]. We have also demon-
strated that total body fat mass, abdominal fat percent-
age, and body lean mass are independent risk factors for
long-term cardiovascular events and mortality in patients
Fig. 2  Exercise parameters over the course of cardiac rehabilitation. HIIT high-intensity interval training, MICT moderate-intensity continuous
training. a Average heart rate during training. HIIT vs. MICT, 2-weeks: 110 vs. 96 bpm, P = .04; 4-weeks: 113 vs. 96 bpm, P = .008; 8-weeks: 116 vs.
98 bpm, P = .009; 12-weeks: 116 vs. 102 bpm, P = .003, respectively. There was no evidence of a difference across groups over time (P = .81). b
Average intensity. 2-weeks: 3.2 vs. 2.6 METs, P = .01; 4-weeks: 3.3 vs. 2.5 METs, P = .01; 8-weeks: 3.5 vs. 2.9 METs, P = .02; 12-weeks: 3.8 vs. 3.2 METs,
P = .03, respectively. Evidence of a difference across groups over time was noted (P = .40). c Duration of exercise. 2-weeks: 31 vs. 25 min, P = .03;
4-weeks: 33 vs. 27 min, P = .008; 8-weeks: 35 vs. 27 min, P = .007; 12-weeks: 34 vs. 30 min, P = .39, respectively. There was no evidence of a difference
across groups over time (P = .68). d Energy expenditure per session. 2-weeks: 143 vs. 98 kcal, P = .09; 4-weeks: 152 vs. 100 kcal, P = .01; 8-weeks: 161
vs. 124 kcal, P = .05; 12-weeks: 163 vs. 143 kcal, P = .41, respectively. There was no evidence of a difference across groups over time (P = .37). Results
presented are mean and 95% confidence limits based on repeated measures ANOVA. Comparisons at each time point are adjusted for multiple
comparisons using the method of Scheffe
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 7 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
Table 2  Outcomes
BMI body mass index, CR cardiac rehabilitation, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-c high-density lipoprotein cholesterol, HIIT high-intensity
interval training, MetS metabolic syndrome, MICT moderate-intensity continuous training, Peak VO2 peak oxygen consumed, PHQ-9 patient health questionnaire 9, SBP
systolic blood pressure, TG triglycerides
MICT (n = 14) HIIT (n = 42) ANCOVA
Baseline Change Baseline Change P-value
Rate-Your-Plate 56 ± 7 5 ± 5 56 ± 7 5 ± 5 P = .46
Average statin 2.4 ± 0.7 0.1 ± 0.3 2.8 ± 0.5 − 0.1 ± 0.5 P = .30
MetS variables
 MetS z-score 5.7 ± 3.6 − 0.8 ± 3.8 4.6 ± 3.4 − 3.6 ± 2.9 P < .001
 ATP III MetS score 3.9 ± 0.7 − 0.6 ± 1.0 3.6 ± 0.6 − 1.2 ± 1.0 P = .005
 Waist circumference, cm 110 ± 11 1 ± 5 110 ± 10 − 3 ± 5 P = .01
 FBG, mg/dl 130.4 ± 38.7 − 3.9 ± 25.8 129.3 ± 37.3 − 25.8 ± 34.8 P < .001
 TG, mg/dl 222.5 ± 80.1 − 10.4 ± 105.3 185.5 ± 101.5 − 67.8 ± 86.7 P < .001
 HDL-c, mg/dl 38.9 ± 10.8 6.4 ± 8.3 40.3 ± 9.8 3.8 ± 9.0 P = .42
 SBP, mmHg 122 ± 18 0 ± 25 122 ± 15 − 6 ± 18 P = .16
 DBP, mmHg 71 ± 12 0 ± 13 68 ± 11 − 7 ± 11 P = .001
Body composition
 Body weight, kg 91.2 ± 14.4 0.6 ± 4.8 91.5 ± 16.3 − 0.5 ± 4.9 P = .45
 BMI, kg/m2
31.5 ± 4.2 0 ± 1.5 31.3 ± 4.7 − 0.1 ± 1.7 P = .83
 Fat mass, kg 35.4 ± 6.6 0 ± 2.2 35.7 ± 8.5 − 2.1 ± 2.1 P = .002
 Body fat, % 40.2 ± 4.9 − 0.2 ± 1.4 39.9 ± 5.9 − 1.8 ± 1.7 P = .002
 Lean mass, kg 53.5 ± 9.3 − 0.9 ± 3.2 53.5 ± 9.8 0.9 ± 1.9 P = .01
 Abdominal fat, % 47.5 ± 5.2 0.1 ± 2.4 49.6 ± 5.7 − 2.2 ± 2.6 P = .004
  Peak ­VO2, ml/kg/min 23.7 ± 7.1 1.4 ± 0.9 23.0 ± 6.3 5.0 ± 2.5 P = .03
 PHQ-9 4.0 ± 2.1 − 1.2 ± 3.6 4.0 ± 3.2 − 1.6 ± 3.5 P = .45
Fig. 3  Changes in metabolic syndrome and body composition variables from the baseline to the completion of 36 sessions of cardiac rehabilitation
across MICT and HIIT groups. ATP III National Cholesterol Education Program’s Adult Treatment Panel III, HIIT high-intensity interval training, MetS
metabolic syndrome, MICT moderate-intensity continuous training. Values are reported as mean ± standard deviation
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 8 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
with [26, 27] and without coronary heart disease (CHD)
[28]. In patients with CHD in the highest quartile of body
fat percentage, risk of cardiovascular events is double
compared to the lowest quartile [27]. In contrast, two
recent studies by Keating et  al. [29] and Wewege et  al.
[30] demonstrated that HIIT and MICT elicited similar
benefits for improvement in body composition for over-
weight and obese adults, especially once controlled for
energy expenditure. Our findings combined with others
support that HIIT may provide similar or enhanced ben-
efits for risk factor management and should be viewed
as an important treatment strategy for MI patients with
MetS.
This study showed that there were no changes in body
mass and BMI in either MICT or HIIT groups, which
are consistent with previous studies by Keating et al. [29]
and Wewege et al. [30] that demonstrated that HIIT and
MICT elicit similar changes in body mass. This phenom-
enon may be related to the obesity paradox. Overweight
and obesity are associated with an increased likelihood of
developing cardiovascular disease and all-cause mortal-
ity [31] and have become increasingly common world-
wide, with overweight and obesity conventionally defined
as a BMI of > 
25 kg/m2
and > 
30 kg/m2
, respectively. In
contrast to the general population, patients with CHD
demonstrate an inverse relationship between BMI and
mortality, termed the obesity paradox [32]. However, it is
now apparent that this paradox is related to the preser-
vation of lean muscle mass as there is no paradox in the
general population [33] or patients with CHD [27] when
measuring body fat percentage instead of BMI. This
point helps to understand how MetS parameters were
improved in our HIIT patients, even in the absence of
BMI changes.
A variety of HIIT protocols have been developed and
used for CHD patients [34], which vary in intensity, inter-
val duration, and the number of intervals. Further, exer-
cise intensity is generally prescribed using a percent of
maximal oxygen consumption, percent of maximal heart
rate, percent of maximal power, or RPE (rated perceived
exertion, Borg scale) [34, 35]. The present study used RPE
to prescribe the intensity of exercise with accompany-
ing HR monitoring. HIIT prescribed using RPE has been
used across the aging spectrum [36, 37]. Buchheit et al.
[38] and Levinger et al. [39] demonstrated that the RPE
has shown a great correlation with HR, ventilation, and
­VO2 in individuals both with and without CAD, and the
correlation is not impacted by beta-blocker medication, a
commonly used HR modulating medication by patients
with MI [39]. In addition, HIIT prescribed by RPE can
promote greater positive responses than both HIIT and
MICT when prescribed with imposed intensity, such as
workload and HR, due to the perceived autonomy, time
efficiency, and changing stimulus [36]. The present study
Table 3  Outcomes after matching for differences in exercise energy expenditure
BMI body mass index, CR cardiac rehabilitation, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-c high-density lipoprotein cholesterol, HIIT high-intensity
interval training, MetS metabolic syndrome, MICT moderate-intensity continuous training, SBP systolic blood pressure, TG triglycerides
MICT (n = 14) HIIT (n = 14) ANCOVA
Baseline Change Baseline Change P-value
Rate-Your-Plate 56 ± 7 5 ± 5 55 ± 7 5 ± 7 P = .95
Average statin 2.4 ± 0.7 0.1 ± 0.3 2.6 ± 0.7 − 0.1 ± 0.3 P = .23
MetS variables
 MetS z-score 5.7 ± 3.6 − 0.8 ± 3.8 5.6 ± 3.2 − 5.3 ± 3.0 P < .001
 ATP III MetS score 4 ± 1 − 1 ± 1 4 ± 0 − 2 ± 1 P = .005
 Waist circumference, cm 110 ± 11 1 ± 5 103 ± 9 − 0.4 ± 2.2 P = .31
 FBG, mg/dl 130.4 ± 38.7 − 3.9 ± 25.8 138.9 ± 46.6 − 40.1 ± 46.6 P = .002
 TG, mg/dl 222.5 ± 80.1 − 10.4 ± 105.3 232.0 ± 111.1 − 97.2 ± 105.7 P = .008
 HDL-c, mg/dl 38.9 ± 10.8 6.4 ± 8.3 37.6 ± 7.3 3.7 ± 4.8 P = .26
 SBP, mmHg 122 ± 18 0 ± 25 122 ± 15 − 13 ± 12 P = .13
 DBP, mmHg 71 ± 12 0 ± 13 70 ± 7 − 12 ± 8 P < .001
Body composition
 Body weight, kg 91.2 ± 14.4 0.6 ± 4.8 80.3 ± 13.2 1.4 ± 7.0 P = .72
 BMI, kg/m2
31.5 ± 4.2 − 0.1 ± 1.5 28.6 ± 4.5 0.7 ± 2.4 P = .92
 Fat mass, kg 35.4 ± 6.6 0 ± 2.2 30.9 ± 7.6 − 1.7 ± 1.8 P = .02
 Body fat, % 40.2 ± 4.9 − 0.2 ± 1.4 38.8 ± 7.5 − 1.8 ± 1.7 P = .01
 Lean mass, kg 53.5 ± 9.3 − 0.9 ± 3.2 48.5 ± 8.5 1.2 ± 1.4 P = .03
 Abdominal fat, % 47.5 ± 5.2 0.1 ± 2.4 48.1 ± 7.4 − 2.4 ± 2.4 P = .01
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 9 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
demonstrates that RPE should be considered an appro-
priate alternative or supplementary method to HR for
prescribing exercise intensity for HIIT in MI patients
with MetS.
To determine the relation of energy intake, statin ther-
apy intensity, and energy expenditure (EE) during exer-
cise and HIIT-induced improvements in MetS and body
composition, the present study assessed dietary quality,
average statin therapy intensity and the EE per exercise
session over the course of 36 sessions of CR. Our results
showed that there were no differences in RYP scores (die-
tary quality) and statin therapy intensity across groups
from baseline to follow-up compared to MICT. Addi-
tionally, HIIT induced similar exercise EEs to MICT at
the beginning and end of 36 CR sessions. These findings
suggest that energy intake, statin therapy intensity, and
EE during exercise are not primary explanations for the
HIIT-induced greater improvements in MetS and body
composition than MICT in these patients. To confirm the
accuracy of these findings, we matched a sub-group of
HIIT and MICT patients on exercise EE specifically and
found that the improvements in MetS and body composi-
tion in the HIIT group persisted.
The exact mechanisms whereby HIIT leads to greater
improvements in MetS variables and body composition
in MI patients with MetS remain unclear. The mecha-
nisms may involve a wide range of systems responsible
for the physiologic adaptations to structured exercise,
including the cardiovascular system, respiratory system,
and musculoskeletal systems. Increasing evidence sug-
gests that HIIT can improve post-infarction left ventricu-
lar remodeling [40], augment stroke volume in patients
with type 2 diabetes [41], optimize heart rate recovery
after exercise in MI patients [42], and improve brachial
artery flow-mediated dilation in sedentary adults [43]
and type 2 diabetes [44, 45], which together may con-
tribute to the improvements in insulin sensitivity, blood
pressure, and body composition [46]. With regards to the
respiratory system, respiratory muscle dysfunction is a
common manifestation in older patients with CVD [47],
Tasoulis et al. demonstrated that 12 weeks of HIIT sig-
nificantly improved respiratory muscle function in older
adults with HF [48]. With respect to skeletal muscle, we
have previously shown that 4-weeks of aerobic exercise
can enhance skeletal muscle mitochondrial biogenesis
and function in male mice [49]. Motta et  al. [50] also
showed that HIIT ameliorated fructose-induced meta-
bolic dysfunction in male mice through mitochondrial
biogenesis and β-oxidation, via irisin and PGC1 α in skel-
etal muscle. Moreover, several recent trials have demon-
strated that 3–12 weeks of HIIT can significantly increase
resting metabolic rate [51] and post-exercise oxygen
consumption in healthy adults [52], and fat oxidation
in obese adolescents [53]. In summary, HIIT can elicit
numerous improvements in organ structure and physi-
ological functions of multiple systems; however, more
research is warranted to better understand the primary
mechanisms of HIIT-induced cardiometabolic benefits.
With respect to the safety of performing HIIT, all par-
ticipants enrolled in this study completed 36 sessions of
CR without a single major adverse event. Although no
major adverse events were registered, the current study
was not designed/powered to demonstrate safety of HIIT
in patients with MI. However, the safety of supervised
HIIT in CR is generally well documented in patients with
established coronary artery disease [54, 55].
Study limitations
It is important to recognize the retrospective, obser-
vational nature of the present study design. Additional
research in this area is encouraged to confirm these
findings in a prospective fashion. To avoid bias associ-
ated with the number of HIIT sessions completed, we
only enrolled the patients who completed the standard
36 sessions of outpatient CR and attended follow-up
assessments, which may have introduced selection bias.
The patients in this study are overweight; therefore,
additional research focusing on MI patients with MetS
within “normal weight” is encouraged. Furthermore,
although not unusual in similar studies, an unintended
consequence of our clinical population is that only 36%
were women. Thus, additional studies may be needed to
ensure the generalizability of our findings.
Conclusions
The present study demonstrates that supervised HIIT
prescribed by RPE can elicit greater improvements in
MetS and body composition for MI patients with MetS
compared to MICT. These findings support the use
of HIIT as a treatment tool to improve MetS compo-
nents in MI patients enrolled in early outpatient cardiac
rehabilitation.
Abbreviations
MetS: metabolic syndrome; MI: myocardial infarction; HIIT: high-intensity
interval training; MICT: moderate-intensity continuous training; CR: cardiac
rehabilitation; DXA: dual-energy x-ray absorptiometry; RPE: rating of perceived
exertion; ACSM: American College of Sports Medicine; HR: heart rate; SBP:
systolic blood pressure; DBP: diastolic blood pressure; ATP III: Adult Treat‑
ment Panel III; TG: triglycerides; FBG: fasting blood glucose; HDL: high density
lipoprotein; RYP: rate your plate; CPET: cardiopulmonary exercise test; 6 MWT:
6 min walk test; VO2peak: maximal oxygen consumption; ANCOVA: analysis
of covariance; ANOVA: analysis of variance; CHD: coronary heart disease; EE:
energy expenditure.
Acknowledgements
We thank the patients and staff of Mayo Clinic Cardiac Rehabilitation Program,
in Rochester, MN, for their valuable contributions to the study.
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 10 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
Authors’contributions
YD, RJT, TPO, RWS and SL are responsible for the conception and design of the
work. YD, TPO, JRM, HH, ARB, JRS and SL contributed to the acquisition or inter‑
pretation of the work. YD and TPO drafted the manuscript. All authors critically
revised the manuscript, gave final approval and agree to be accountable for
all aspects of the work ensuring integrity and accuracy. All authors read and
approved the final manuscript.
Funding
The present study was supported in part by grants from the National Institutes
of Health (HL-126638 to TPO) and Hunan Development and Reform Commis‑
sion Foundation of China (Grant no. [2012] 1521 to SL).
Availability of data and materials
Not applicable.
Ethics approval and consent to participate
Approval was received from the Mayo Clinic Institutional Review Board and
authorization for the usage of medical records was obtained.
Consent for publication
It was obtained through authorization of the use of medical records by the
patients.
Competing interests
The authors declare that they have no competing interests.
Received: 14 May 2019 Accepted: 7 August 2019
References
	1.	 Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA,
Gordon DJ, Krauss RM, Savage PJ, Smith SC Jr, et al. Diagnosis and man‑
agement of the metabolic syndrome: an American Heart Association/
National Heart, Lung, and Blood Institute Scientific Statement. Circulation.
2005;112(17):2735–52.
	2.	 Hu H, Nakagawa T, Honda T, Yamamoto S, Nanri A, Konishi M, Okazaki H,
Kuwahara K, Hori A, Nishiura C, et al. Metabolic syndrome over 4 years
before the onset of cardiovascular disease-nested case–control study.
Circ J. 2018;82(2):430–6.
	3.	 Cavallari I, Cannon CP, Braunwald E, Goodrich EL, Im K, Lukas MA,
O’Donoghue ML. Metabolic syndrome and the risk of adverse cardio‑
vascular events after an acute coronary syndrome. Eur J Prev Cardiol.
2018;25(8):830–8.
	4.	 Han TS, Lean ME. A clinical perspective of obesity, metabolic
syndrome and cardiovascular disease. JRSM Cardiovasc Dis.
2016;5:2048004016633371.
	5.	 Fihn SD, Gardin JM, Abrams J, Berra K, Blankenship JC, Dallas AP, Douglas
PS, Foody JM, Gerber TC, Hinderliter AL, et al. 2012 ACCF/AHA/ACP/AATS/
PCNA/SCAI/STS guideline for the diagnosis and management of patients
with stable ischemic heart disease: a report of the American College
of Cardiology Foundation/American Heart Association task force on
practice guidelines, and the American College of Physicians, American
Association for Thoracic Surgery, Preventive Cardiovascular Nurses Asso‑
ciation, Society for Cardiovascular Angiography and Interventions, and
Society of Thoracic Surgeons. Circulation. 2012;126(25):e354–471.
	6.	 Ostman C, Smart NA, Morcos D, Duller A, Ridley W, Jewiss D. The effect
of exercise training on clinical outcomes in patients with the metabolic
syndrome: a systematic review and meta-analysis. Cardiovasc Diabetol.
2017;16(1):110.
	7.	 Amadid H, Johansen NB, Bjerregaard AL, Brage S, Faerch K, Lauritzen T,
Witte DR, Sandbaek A, Jorgensen ME, Vistisen D. The role of physical activ‑
ity in the development of first cardiovascular disease event: a tree-struc‑
tured survival analysis of the Danish ADDITION-PRO cohort. Cardiovasc
Diabetol. 2018;17(1):126.
	8.	 Ramos JS, Dalleck LC, Borrani F, Beetham KS, Wallen MP, Mallard AR, Clark
B, Gomersall S, Keating SE, Fassett RG, et al. Low-volume high-intensity
interval training is sufficient to ameliorate the severity of metabolic
syndrome. Metab Syndr Relat Disord. 2017;15(7):319–28.
	9.	 Grace A, Chan E, Giallauria F, Graham PL, Smart NA. Clinical outcomes
and glycaemic responses to different aerobic exercise training intensities
in type II diabetes: a systematic review and meta-analysis. Cardiovasc
Diabetol. 2017;16(1):37.
	10.	 Choi HY, Han HJ, Choi JW, Jung HY, Joa KL. Superior effects of high-inten‑
sity interval training compared to conventional therapy on cardiovascular
and psychological aspects in myocardial infarction. Ann Rehabil Med.
2018;42(1):145–53.
	11.	 Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM,
Nieman DC, Swain DP, American College of Sports Medicine position
stand. Quantity and quality of exercise for developing and maintaining
cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently
healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc.
2011;43(7):1334–59.
	12.	 Ainsworth BE, Haskell WL, Herrmann SD, Meckes N, Bassett DR Jr, Tudor-
Locke C, Greer JL, Vezina J, Whitt-Glover MC, Leon AS. 2011 compendium
of physical activities: a second update of codes and MET values. Med Sci
Sports Exerc. 2011;43(8):1575–81.
	13.	 Dieli-Conwright CM, Courneya KS, Demark-Wahnefried W, Sami N, Lee K,
Buchanan TA, Spicer DV, Tripathy D, Bernstein L, Mortimer JE. Effects of
aerobic and resistance exercise on metabolic syndrome, sarcopenic obe‑
sity, and circulating biomarkers in overweight or obese survivors of breast
cancer: a randomized controlled trial. J Clin Oncol. 2018;36(9):875–83.
	14.	 Imboden MT, Welch WA, Swartz AM, Montoye AH, Finch HW, Harber
MP, Kaminsky LA. Reference standards for body fat measures using
GE dual energy x-ray absorptiometry in Caucasian adults. PLoS ONE.
2017;12(4):e0175110.
	15.	 Gans KM, Hixson ML, Eaton CB, Lasater TM. Rate your plate: a dietary
assessment and educational tool for blood cholesterol control. Nutr Clin
Care. 2000;3(3):163–9.
	16.	 Stone NJ, Robinson JG, Lichtenstein AH, Bairey Merz CN, Blum CB, Eckel
RH, Goldberg AC, Gordon D, Levy D, Lloyd-Jones DM, et al. 2013 ACC/
AHA guideline on the treatment of blood cholesterol to reduce athero‑
sclerotic cardiovascular risk in adults: a report of the American College of
Cardiology/American Heart Association Task Force on Practice Guidelines.
J Am Coll Cardiol. 2014;63(25 Pt B):2889–934.
	17.	 Ross RM, Murthy JN, Wollak ID, Jackson AS. The six minute walk test accu‑
rately estimates mean peak oxygen uptake. BMC Pulm Med. 2010;10:31.
	18.	 Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression
severity measure. J Gen Intern Med. 2001;16(9):606–13.
	19.	 Morales-Palomo F, Ramirez-Jimenez M, Ortega JF, Mora-Rodriguez R.
Exercise periodization over the year improves metabolic syndrome and
medication use. Med Sci Sports Exerc. 2018;50(10):1983–91.
	20.	 Alvarez C, Ramirez-Velez R, Ramirez-Campillo R, Lucia A, Alonso-Martinez
AM, Faundez H, Cadore EL, Izquierdo M. Improvements cardiometabolic
risk factors in Latin American Amerindians (the Mapuche) with concur‑
rent training. Scand J Med Sci Sports. 2019;29(6):886–96.
	21.	 Tjonna AE, Stolen TO, Bye A, Volden M, Slordahl SA, Odegard R, Skogvoll
E, Wisloff U. Aerobic interval training reduces cardiovascular risk factors
more than a multitreatment approach in overweight adolescents. Clin
Sci. 2009;116(4):317–26.
	22.	 Boudou P, Sobngwi E, Mauvais-Jarvis F, Vexiau P, Gautier JF. Absence of
exercise-induced variations in adiponectin levels despite decreased
abdominal adiposity and improved insulin sensitivity in type 2 diabetic
men. Eur J Endocrinol. 2003;149(5):421–4.
	23.	 Trapp EG, Chisholm DJ, Freund J, Boutcher SH. The effects of high-inten‑
sity intermittent exercise training on fat loss and fasting insulin levels of
young women. Int J Obes. 2008;32(4):684–91.
	24.	 Kim K, Park SM. Association of muscle mass and fat mass with insulin
resistance and the prevalence of metabolic syndrome in Korean adults: a
cross-sectional study. Sci Rep. 2018;8(1):2703.
	25.	 Kwon H, Kim D, Kim JS. Body fat distribution and the risk of incident met‑
abolic syndrome: a longitudinal cohort study. Sci Rep. 2017;7(1):10955.
	26.	 Medina-Inojosa JR, Batsis JA, Supervia M, Somers VK, Thomas RJ, Jenkins
S, Grimes C, Lopez-Jimenez F. Relation of waist–hip ratio to long-term car‑
diovascular events in patients with coronary artery disease. Am J Cardiol.
2018;121(8):903–9.
	27.	 Medina-Inojosa JR, Somers VK, Thomas RJ, Jean N, Jenkins SM,
Gomez-Ibarra MA, Supervia M, Lopez-Jimenez F. Association between
adiposity and lean mass with long-term cardiovascular events in
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
Page 11 of 11
Dun et al. Cardiovasc Diabetol (2019) 18:104
• fast, convenient online submission
• thorough peer review by experienced researchers in your field
• rapid publication on acceptance
• support for research data, including large and complex data types
• gold Open Access which fosters wider collaboration and increased citations
maximum visibility for your research: over 100M website views per year
•
At BMC, research is always in progress.
Learn more biomedcentral.com/submissions
Ready to submit your research ? Choose BMC and benefit from:
patients with coronary artery disease: no paradox. J Am Heart Assoc.
2018;7(10):e007505. https​://doi.org/10.1161/JAHA.117.00750​7.
	28.	 Padwal R, Leslie WD, Lix LM, Majumdar SR. Relationship among body fat
percentage, body mass index, and all-cause mortality: a cohort study.
Ann Intern Med. 2016;164(8):532–41.
	29.	 Keating SE, Johnson NA, Mielke GI, Coombes JS. A systematic review and
meta-analysis of interval training versus moderate-intensity continuous
training on body adiposity. Obes Rev. 2017;18(8):943–64.
	30.	 Wewege M, van den Berg R, Ward RE, Keech A. The effects of high-inten‑
sity interval training vs. moderate-intensity continuous training on body
composition in overweight and obese adults: a systematic review and
meta-analysis. Obes Rev. 2017;18(6):635–46.
	31.	 Preston SH, Vierboom YC, Stokes A. The role of obesity in excep‑
tionally slow US mortality improvement. Proc Natl Acad Sci USA.
2018;115(5):957–61.
	32.	 Romero-Corral A, Montori VM, Somers VK, Korinek J, Thomas RJ, Allison
TG, Mookadam F, Lopez-Jimenez F. Association of bodyweight with total
mortality and with cardiovascular events in coronary artery disease: a
systematic review of cohort studies. Lancet. 2006;368(9536):666–78.
	33.	 Dong B, Peng Y, Wang Z, Adegbija O, Hu J, Ma J, Ma YH. Joint associa‑
tion between body fat and its distribution with all-cause mortality: a
data linkage cohort study based on NHANES (1988–2011). PLoS ONE.
2018;13(2):e0193368.
	34.	 Ribeiro PAB, Boidin M, Juneau M, Nigam A, Gayda M. High-intensity inter‑
val training in patients with coronary heart disease: prescription models
and perspectives. Ann Phys Rehabil Med. 2017;60(1):50–7.
	35.	 Dun Y, Smith JR, Liu S, Olson TP. High-intensity interval training in cardiac
rehabilitations. Clin Geriatr Med. 2019 (in press).
	36.	 Thum JS, Parsons G, Whittle T, Astorino TA. High-intensity interval training
elicits higher enjoyment than moderate intensity continuous exercise.
PLoS ONE. 2017;12(1):e0166299.
	37.	 Viana AA, Fernandes B, Alvarez C, Guimaraes GV, Ciolac EG. Prescribing
high-intensity interval exercise by RPE in individuals with type 2 diabetes:
metabolic and hemodynamic responses. Appl Physiol Nutr Metab.
2019;44(4):348–56.
	38.	 Buchheit M, Laursen PB. High-intensity interval training, solutions to the
programming puzzle: part I: cardiopulmonary emphasis. Sports Med.
2013;43(5):313–38.
	39.	 Levinger I, Bronks R, Cody DV, Linton I, Davie A. Perceived exertion as
an exercise intensity indicator in chronic heart failure patients on Beta-
blockers. J Sports Sci Med. 2004;3(YISI 1):23–7.
	40.	 Godfrey R, Theologou T, Dellegrottaglie S, Binukrishnan S, Wright J, Whyte
G, Ellison G. The effect of high-intensity aerobic interval training on
postinfarction left ventricular remodelling. BMJ Case Rep. 2013. https​://
doi.org/10.1136/bcr-2012-00766​8.
	41.	 Wilson GA, Wilkins GT, Cotter JD, Lamberts RR, Lal S, Baldi JC. Impaired
ventricular filling limits cardiac reserve during submaximal exercise in
people with type 2 diabetes. Cardiovasc Diabetol. 2017;16(1):160.
	42.	 Boidin M, Gayda M, Henri C, Hayami D, Trachsel LD, Besnier F, Lalonge
J, Juneau M, Nigam A. Effects of interval training on risk markers
for arrhythmic death: a randomized controlled trial. Clin Rehabil.
2019;33(8):1320–30.
	43.	 Ramirez-Velez R, Hernandez-Quinones PA, Tordecilla-Sanders A, Alvarez C,
Ramirez-Campillo R, Izquierdo M, Correa-Bautista JE, Garcia-Hermoso A,
Garcia RG. Effectiveness of HIIT compared to moderate continuous train‑
ing in improving vascular parameters in inactive adults. Lipids Health Dis.
2019;18(1):42.
	44.	 Hollekim-Strand SM, Bjorgaas MR, Albrektsen G, Tjonna AE, Wisloff
U, Ingul CB. High-intensity interval exercise effectively improves
cardiac function in patients with type 2 diabetes mellitus and dias‑
tolic dysfunction: a randomized controlled trial. J Am Coll Cardiol.
2014;64(16):1758–60.
	45.	 Qiu S, Cai X, Yin H, Sun Z, Zugel M, Steinacker JM, Schumann U. Exercise
training and endothelial function in patients with type 2 diabetes: a
meta-analysis. Cardiovasc Diabetol. 2018;17(1):64.
	46.	 Campbell WW, Kraus WE, Powell KE, Haskell WL, Janz KF, Jakicic JM,
Troiano RP, Sprow K, Torres A, Piercy KL, et al. High-intensity interval
training for cardiometabolic disease prevention. Med Sci Sports Exerc.
2019;51(6):1220–6.
	47.	 Verissimo P, Casalaspo TJ, Goncalves LH, Yang AS, Eid RC, Timenetsky KT.
High prevalence of respiratory muscle weakness in hospitalized acute
heart failure elderly patients. PLoS ONE. 2015;10(2):e0118218.
	48.	 Tasoulis A, Papazachou O, Dimopoulos S, Gerovasili V, Karatzanos E,
Kyprianou T, Drakos S, Anastasiou-Nana M, Roussos C, Nanas S. Effects
of interval exercise training on respiratory drive in patients with chronic
heart failure. Respir Med. 2010;104(10):1557–65.
	49.	 Dun Y, Liu S, Zhang W, Xie M, Qiu L. Exercise combined with Rhodiola
sacra supplementation improves exercise capacity and ameliorates
exhaustive exercise-induced muscle damage through enhancement of
mitochondrial quality control. Oxid Med Cell Longev. 2017;2017:8024857.
	50.	 Motta VF, Bargut TL, Aguila MB, Mandarim-de-Lacerda CA. Treating
fructose-induced metabolic changes in mice with high-intensity interval
training: insights in the liver, white adipose tissue, and skeletal muscle. J
Appl Physiol (1985). 2017;123(4):699–709.
	51.	 Schubert MM, Clarke HE, Seay RF, Spain KK. Impact of 4 weeks of interval
training on resting metabolic rate, fitness, and health-related outcomes.
Appl Physiol Nutr Metab. 2017;42(10):1073–81.
	52.	 Schleppenbach LN, Ezer AB, Gronemus SA, Widenski KR, Braun SI, Janot
JM. Speed- and circuit-based high-intensity interval training on recovery
oxygen consumption. Int J Exerc Sci. 2017;10(7):942–53.
	53.	 Lazzer S, Tringali G, Caccavale M, De Micheli R, Abbruzzese L, Sartorio
A. Effects of high-intensity interval training on physical capacities and
substrate oxidation rate in obese adolescents. J Endocrinol Invest.
2017;40(2):217–26.
	54.	 Authors/Task Force M, Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C,
Catapano AL, Cooney MT, Corra U, Cosyns B, et al. 2016 European Guide‑
lines on cardiovascular disease prevention in clinical practice: the Sixth
Joint Task Force of the European Society of Cardiology and Other Socie‑
ties on Cardiovascular Disease Prevention in Clinical Practice (constituted
by representatives of 10 societies and by invited experts) Developed with
the special contribution of the European Association for Cardiovascular
Prevention & Rehabilitation (EACPR). Atherosclerosis. 2016;252:207–74.
	55.	 Rognmo O, Moholdt T, Bakken H, Hole T, Molstad P, Myhr NE, Grimsmo
J, Wisloff U. Cardiovascular risk of high- versus moderate-intensity
aerobic exercise in coronary heart disease patients. Circulation.
2012;126(12):1436–40.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in pub‑
lished maps and institutional affiliations.
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
1.
2.
3.
4.
5.
6.
Terms and Conditions
Springer Nature journal content, brought to you courtesy of Springer Nature Customer Service Center GmbH (“Springer Nature”).
Springer Nature supports a reasonable amount of sharing of research papers by authors, subscribers and authorised users (“Users”), for small-
scale personal, non-commercial use provided that all copyright, trade and service marks and other proprietary notices are maintained. By
accessing, sharing, receiving or otherwise using the Springer Nature journal content you agree to these terms of use (“Terms”). For these
purposes, Springer Nature considers academic use (by researchers and students) to be non-commercial.
These Terms are supplementary and will apply in addition to any applicable website terms and conditions, a relevant site licence or a personal
subscription. These Terms will prevail over any conflict or ambiguity with regards to the relevant terms, a site licence or a personal subscription
(to the extent of the conflict or ambiguity only). For Creative Commons-licensed articles, the terms of the Creative Commons license used will
apply.
We collect and use personal data to provide access to the Springer Nature journal content. We may also use these personal data internally within
ResearchGate and Springer Nature and as agreed share it, in an anonymised way, for purposes of tracking, analysis and reporting. We will not
otherwise disclose your personal data outside the ResearchGate or the Springer Nature group of companies unless we have your permission as
detailed in the Privacy Policy.
While Users may use the Springer Nature journal content for small scale, personal non-commercial use, it is important to note that Users may
not:
use such content for the purpose of providing other users with access on a regular or large scale basis or as a means to circumvent access
control;
use such content where to do so would be considered a criminal or statutory offence in any jurisdiction, or gives rise to civil liability, or is
otherwise unlawful;
falsely or misleadingly imply or suggest endorsement, approval , sponsorship, or association unless explicitly agreed to by Springer Nature in
writing;
use bots or other automated methods to access the content or redirect messages
override any security feature or exclusionary protocol; or
share the content in order to create substitute for Springer Nature products or services or a systematic database of Springer Nature journal
content.
In line with the restriction against commercial use, Springer Nature does not permit the creation of a product or service that creates revenue,
royalties, rent or income from our content or its inclusion as part of a paid for service or for other commercial gain. Springer Nature journal
content cannot be used for inter-library loans and librarians may not upload Springer Nature journal content on a large scale into their, or any
other, institutional repository.
These terms of use are reviewed regularly and may be amended at any time. Springer Nature is not obligated to publish any information or
content on this website and may remove it or features or functionality at our sole discretion, at any time with or without notice. Springer Nature
may revoke this licence to you at any time and remove access to any copies of the Springer Nature journal content which have been saved.
To the fullest extent permitted by law, Springer Nature makes no warranties, representations or guarantees to Users, either express or implied
with respect to the Springer nature journal content and all parties disclaim and waive any implied warranties or warranties imposed by law,
including merchantability or fitness for any particular purpose.
Please note that these rights do not automatically extend to content, data or other material published by Springer Nature that may be licensed
from third parties.
If you would like to use or distribute our Springer Nature journal content to a wider audience or on a regular basis or in any other manner not
expressly permitted by these Terms, please contact Springer Nature at
onlineservice@springernature.com

More Related Content

What's hot

3. combined exercise and inspiratory muscle training in patients
3. combined exercise and inspiratory muscle training in patients3. combined exercise and inspiratory muscle training in patients
3. combined exercise and inspiratory muscle training in patientsHibaAnis2
 
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...guestaf1e4
 
Cardiac rehabilitation
Cardiac rehabilitationCardiac rehabilitation
Cardiac rehabilitationmrinal joshi
 
Cardiac Rehabilitation
Cardiac RehabilitationCardiac Rehabilitation
Cardiac Rehabilitationguest785be1
 
2. exercise prescription for patients with acute coronary syndrome
2. exercise prescription for patients with acute coronary syndrome2. exercise prescription for patients with acute coronary syndrome
2. exercise prescription for patients with acute coronary syndromeHibaAnis2
 
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...guestaf1e4
 
Cardiac rehabilitation (1)
Cardiac rehabilitation (1)Cardiac rehabilitation (1)
Cardiac rehabilitation (1)Archana Morey
 
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...LucyPi1
 
Cardiac rehab, telehealth, the evidence for alternatives for ACOs
Cardiac rehab, telehealth, the evidence for alternatives for ACOsCardiac rehab, telehealth, the evidence for alternatives for ACOs
Cardiac rehab, telehealth, the evidence for alternatives for ACOsMaxpowerjr
 
Phase 1of cardiac rehabilitation ppt x
Phase 1of cardiac rehabilitation ppt xPhase 1of cardiac rehabilitation ppt x
Phase 1of cardiac rehabilitation ppt xQuratBenu1
 

What's hot (20)

3. combined exercise and inspiratory muscle training in patients
3. combined exercise and inspiratory muscle training in patients3. combined exercise and inspiratory muscle training in patients
3. combined exercise and inspiratory muscle training in patients
 
Ijpr.2016.129
Ijpr.2016.129Ijpr.2016.129
Ijpr.2016.129
 
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...
Economic And Humanistic Outcomes Of Post Acs In Cardiac Rehabilitation Progra...
 
Cardiac rehabilitation
Cardiac rehabilitationCardiac rehabilitation
Cardiac rehabilitation
 
Diss Pub View
Diss Pub ViewDiss Pub View
Diss Pub View
 
Cardiac Rehabilitation
Cardiac RehabilitationCardiac Rehabilitation
Cardiac Rehabilitation
 
2. exercise prescription for patients with acute coronary syndrome
2. exercise prescription for patients with acute coronary syndrome2. exercise prescription for patients with acute coronary syndrome
2. exercise prescription for patients with acute coronary syndrome
 
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...
 
Cardiac rehabilitation
Cardiac rehabilitationCardiac rehabilitation
Cardiac rehabilitation
 
Cardiac rehabilitation (1)
Cardiac rehabilitation (1)Cardiac rehabilitation (1)
Cardiac rehabilitation (1)
 
Cardiac Rehabilitation
Cardiac Rehabilitation Cardiac Rehabilitation
Cardiac Rehabilitation
 
Stroke
StrokeStroke
Stroke
 
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...
Acupuncture and/or moxibustion for the treatment of lumbar disc herniation: q...
 
Cardiac rehabilitation
Cardiac rehabilitationCardiac rehabilitation
Cardiac rehabilitation
 
Cardiac rehab, telehealth, the evidence for alternatives for ACOs
Cardiac rehab, telehealth, the evidence for alternatives for ACOsCardiac rehab, telehealth, the evidence for alternatives for ACOs
Cardiac rehab, telehealth, the evidence for alternatives for ACOs
 
Effect of Sports on Blood Pressure and Heart Rate Variability: An Interventio...
Effect of Sports on Blood Pressure and Heart Rate Variability: An Interventio...Effect of Sports on Blood Pressure and Heart Rate Variability: An Interventio...
Effect of Sports on Blood Pressure and Heart Rate Variability: An Interventio...
 
Cardiac rehabitalization ppt
Cardiac rehabitalization pptCardiac rehabitalization ppt
Cardiac rehabitalization ppt
 
Cardiac rehabilitation
Cardiac rehabilitationCardiac rehabilitation
Cardiac rehabilitation
 
Effect of Meditation on Respiratory System, Cardiovascular System and Lipid P...
Effect of Meditation on Respiratory System, Cardiovascular System and Lipid P...Effect of Meditation on Respiratory System, Cardiovascular System and Lipid P...
Effect of Meditation on Respiratory System, Cardiovascular System and Lipid P...
 
Phase 1of cardiac rehabilitation ppt x
Phase 1of cardiac rehabilitation ppt xPhase 1of cardiac rehabilitation ppt x
Phase 1of cardiac rehabilitation ppt x
 

Similar to High intensity interval-training improves metabolic syndrome

Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...
Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...
Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...ssuser4701fb
 
Global health 2018_3_30_70034
Global health 2018_3_30_70034Global health 2018_3_30_70034
Global health 2018_3_30_70034Zahra SADEK
 
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...Yogacharya AB Bhavanani
 
International Journal of Pharmaceutical Science Invention (IJPSI)
International Journal of Pharmaceutical Science Invention (IJPSI)International Journal of Pharmaceutical Science Invention (IJPSI)
International Journal of Pharmaceutical Science Invention (IJPSI)inventionjournals
 
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Yogacharya AB Bhavanani
 
Impact of a designed nursing intervention protocol on myocardial infarction p...
Impact of a designed nursing intervention protocol on myocardial infarction p...Impact of a designed nursing intervention protocol on myocardial infarction p...
Impact of a designed nursing intervention protocol on myocardial infarction p...Alexander Decker
 
Respiratory muscle training...
Respiratory muscle training...Respiratory muscle training...
Respiratory muscle training...Kimberly Walsh
 
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Yogacharya AB Bhavanani
 
Effect of Post-MI Exercise-Final Draft
Effect of Post-MI Exercise-Final DraftEffect of Post-MI Exercise-Final Draft
Effect of Post-MI Exercise-Final DraftCastural Thompson
 
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...IOSR Journals
 
Medical Exercise Training: The New Modality
Medical Exercise Training: The New ModalityMedical Exercise Training: The New Modality
Medical Exercise Training: The New ModalityMichael Jones, PhD, PT
 
Exercise Training Recommendation For Individual With Left Ventricular Assisti...
Exercise Training Recommendation For Individual With Left Ventricular Assisti...Exercise Training Recommendation For Individual With Left Ventricular Assisti...
Exercise Training Recommendation For Individual With Left Ventricular Assisti...Javidsultandar
 
Supervised exercise and diabetes and oxidative stress
Supervised exercise and diabetes and oxidative stressSupervised exercise and diabetes and oxidative stress
Supervised exercise and diabetes and oxidative stresssenthil kumar Elumalai
 
1. Phase -1 Cardiac Rehabilitation in CABG patients.
1. Phase -1 Cardiac Rehabilitation in CABG patients.1. Phase -1 Cardiac Rehabilitation in CABG patients.
1. Phase -1 Cardiac Rehabilitation in CABG patients.ShagufaAmber
 

Similar to High intensity interval-training improves metabolic syndrome (20)

Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...
Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...
Optimizing Outcomes in Cardiac Rehabilitation The Importance of Exercise Inte...
 
Poster presentation Royal Society Of Medicine London
Poster presentation Royal Society Of Medicine LondonPoster presentation Royal Society Of Medicine London
Poster presentation Royal Society Of Medicine London
 
Global health 2018_3_30_70034
Global health 2018_3_30_70034Global health 2018_3_30_70034
Global health 2018_3_30_70034
 
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...
IMMEDIATE EFFECT OF CHANDRANADI PRANAYAM ON HEART RATE VARIABILITY AND CARDIO...
 
Poster presentation rsm london
Poster presentation rsm londonPoster presentation rsm london
Poster presentation rsm london
 
International Journal of Pharmaceutical Science Invention (IJPSI)
International Journal of Pharmaceutical Science Invention (IJPSI)International Journal of Pharmaceutical Science Invention (IJPSI)
International Journal of Pharmaceutical Science Invention (IJPSI)
 
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
 
Cardio vascular functional capacity and reactivity to exercise in Normotensiv...
Cardio vascular functional capacity and reactivity to exercise in Normotensiv...Cardio vascular functional capacity and reactivity to exercise in Normotensiv...
Cardio vascular functional capacity and reactivity to exercise in Normotensiv...
 
Stroke robot assisted therapy
Stroke robot assisted therapyStroke robot assisted therapy
Stroke robot assisted therapy
 
Impact of a designed nursing intervention protocol on myocardial infarction p...
Impact of a designed nursing intervention protocol on myocardial infarction p...Impact of a designed nursing intervention protocol on myocardial infarction p...
Impact of a designed nursing intervention protocol on myocardial infarction p...
 
Respiratory muscle training...
Respiratory muscle training...Respiratory muscle training...
Respiratory muscle training...
 
Ecercise in
Ecercise in Ecercise in
Ecercise in
 
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
Randomized controlled trial of 12-week yoga therapy as lifestyle intervention...
 
Effect of Post-MI Exercise-Final Draft
Effect of Post-MI Exercise-Final DraftEffect of Post-MI Exercise-Final Draft
Effect of Post-MI Exercise-Final Draft
 
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...
Assess The Effect of Resistance Training Compared To a Weight Loss Diet Progr...
 
Medical Exercise Training: The New Modality
Medical Exercise Training: The New ModalityMedical Exercise Training: The New Modality
Medical Exercise Training: The New Modality
 
Exercise Training Recommendation For Individual With Left Ventricular Assisti...
Exercise Training Recommendation For Individual With Left Ventricular Assisti...Exercise Training Recommendation For Individual With Left Ventricular Assisti...
Exercise Training Recommendation For Individual With Left Ventricular Assisti...
 
Exercise-and-MS-(1).pptx
Exercise-and-MS-(1).pptxExercise-and-MS-(1).pptx
Exercise-and-MS-(1).pptx
 
Supervised exercise and diabetes and oxidative stress
Supervised exercise and diabetes and oxidative stressSupervised exercise and diabetes and oxidative stress
Supervised exercise and diabetes and oxidative stress
 
1. Phase -1 Cardiac Rehabilitation in CABG patients.
1. Phase -1 Cardiac Rehabilitation in CABG patients.1. Phase -1 Cardiac Rehabilitation in CABG patients.
1. Phase -1 Cardiac Rehabilitation in CABG patients.
 

Recently uploaded

Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...CALL GIRLS
 
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort ServicePremium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Servicevidya singh
 
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.MiadAlsulami
 
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...Taniya Sharma
 
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Service
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls ServiceCall Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Service
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Servicenarwatsonia7
 
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escorts
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore EscortsCall Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escorts
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escortsvidya singh
 
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...Miss joya
 
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Delivery
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on DeliveryCall Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Delivery
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Deliverynehamumbai
 
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoy
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night EnjoyCall Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoy
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoynarwatsonia7
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...narwatsonia7
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...narwatsonia7
 
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...Call girls in Ahmedabad High profile
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoybabeytanya
 
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...Miss joya
 
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...Miss joya
 
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune) Girls Service
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune)  Girls ServiceCALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune)  Girls Service
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune) Girls ServiceMiss joya
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatorenarwatsonia7
 

Recently uploaded (20)

Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
 
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort ServicePremium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
Premium Call Girls Cottonpet Whatsapp 7001035870 Independent Escort Service
 
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
Russian Call Girls in Delhi Tanvi ➡️ 9711199012 💋📞 Independent Escort Service...
 
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.
 
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...
💎VVIP Kolkata Call Girls Parganas🩱7001035870🩱Independent Girl ( Ac Rooms Avai...
 
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Service
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls ServiceCall Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Service
Call Girls Service Bellary Road Just Call 7001305949 Enjoy College Girls Service
 
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escorts
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore EscortsCall Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escorts
Call Girls Horamavu WhatsApp Number 7001035870 Meeting With Bangalore Escorts
 
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...
Russian Call Girls in Pune Tanvi 9907093804 Short 1500 Night 6000 Best call g...
 
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Delivery
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on DeliveryCall Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Delivery
Call Girls Colaba Mumbai ❤️ 9920874524 👈 Cash on Delivery
 
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoy
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night EnjoyCall Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoy
Call Girls Yelahanka Bangalore 📲 9907093804 💞 Full Night Enjoy
 
sauth delhi call girls in Bhajanpura 🔝 9953056974 🔝 escort Service
sauth delhi call girls in Bhajanpura 🔝 9953056974 🔝 escort Servicesauth delhi call girls in Bhajanpura 🔝 9953056974 🔝 escort Service
sauth delhi call girls in Bhajanpura 🔝 9953056974 🔝 escort Service
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
 
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...
Call Girls Service Navi Mumbai Samaira 8617697112 Independent Escort Service ...
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
 
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...
Russian Call Girls in Pune Riya 9907093804 Short 1500 Night 6000 Best call gi...
 
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...
College Call Girls Pune Mira 9907093804 Short 1500 Night 6000 Best call girls...
 
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCREscort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
 
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune) Girls Service
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune)  Girls ServiceCALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune)  Girls Service
CALL ON ➥9907093804 🔝 Call Girls Hadapsar ( Pune) Girls Service
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
 

High intensity interval-training improves metabolic syndrome

  • 1. Dun et al. Cardiovasc Diabetol (2019) 18:104 https://doi.org/10.1186/s12933-019-0907-0 ORIGINAL INVESTIGATION High‑intensity interval training improves metabolic syndrome and body composition in outpatient cardiac rehabilitation patients with myocardial infarction Yaoshan Dun1,2 , Randal J. Thomas2 , Joshua R. Smith2 , Jose R. Medina‑Inojosa2 , Ray W. Squires2 , Amanda R. Bonikowske2 , Hsuhang Huang2 , Suixin Liu1* and Thomas P. Olson2* Abstract  Background:  To examine the effect of high-intensity interval training (HIIT) on metabolic syndrome (MetS) and body composition in cardiac rehabilitation (CR) patients with myocardial infarction (MI). Methods:  We retrospectively screened 174 consecutive patients with MetS enrolled in CR following MI between 2015 and 2018. We included 56 patients who completed 36 CR sessions and pre-post dual-energy X-ray absorptiom‑ etry. Of these patients, 42 engaged in HIIT and 14 in moderate-intensity continuous training (MICT). HIIT included 4–8 intervals of high-intensity (30–60 s at RPE 15–17 [Borg 6–20]) and low-intensity (1–5 min at RPE < 14), and MICT included 20–45 min of exercise at RPE 12–14. MetS and body composition variables were compared between MICT and HIIT groups. Results:  Compared to MICT, HIIT demonstrated greater reductions in MetS (relative risk = 0.5, 95% CI 0.33–0.75, P < .001), MetS z-score (− 3.6 ± 2.9 vs. − 0.8 ± 3.8, P < .001) and improved MetS components: waist circumference (− 3 ± 5 vs. 1 ± 5 cm, P = .01), fasting blood glucose (− 25.8 ± 34.8 vs. − 3.9 ± 25.8 mg/dl, P < .001), triglycerides (− 67.8 ± 86.7 vs. − 10.4 ± 105.3 mg/dl, P < .001), and diastolic blood pressure (− 7 ± 11 vs. 0 ± 13 mmHg, P = .001). HIIT group demonstrated greater reductions in body fat mass (− 2.1 ± 2.1 vs. 0 ± 2.2 kg, P = .002), with increased body lean mass (0.9 ± 1.9 vs. − 0.9 ± 3.2 kg, P = .01) than the MICT. After matching for exercise energy expenditure, HIIT- induced improvements persisted for MetS z-score (P < .001), MetS components (P < .05), body fat mass (P = .002), body fat (P = .01), and lean mass (P = .03). Conclusions:  Our data suggest that, compared to MICT, supervised HIIT results in greater improvements in MetS and body composition in MI patients with MetS undergoing CR. Keywords:  Cardiac rehabilitation, High-intensity interval training, Metabolic syndrome, Myocardial infarction, Body composition © The Author(s) 2019. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creat​iveco​mmons​.org/licen​ses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creat​iveco​mmons​.org/ publi​cdoma​in/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Open Access Cardiovascular Diabetology *Correspondence: liusuixin@csu.edu.cn; olson.thomas2@mayo.edu 1 Division of Cardiac Rehabilitation, Department of Physical Medicine & Rehabilitation, Xiangya Hospital Central South University, 87 Xiangya Road, Changsha, Hunan, People’s Republic of China 2 Division of Preventive Cardiology, Department of Cardiovascular Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 2. Page 2 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 Background Metabolic syndrome (MetS) is a constellation of cardio- vascular risk factors that include abdominal adiposity, impaired glucose tolerance, hypertension, low serum high-density lipoprotein cholesterol and hypertriglyc- eridemia [1], and is associated with an eightfold increase in the risk of myocardial infarction (MI) [2]. Presence of MetS in patients with MI is associated with increased risk of adverse cardiovascular events and recurrent MI [3]. Obesity, especially abdominal adiposity is also consid- ered an initial and principal pathophysiologic component of MetS [4]. More effective interventions to ameliorate MetS and reduce body fat among survivors of MI are critical to improving MI outcomes. Current guidelines recommend exercise training as adjunctive therapy in patients with MI [5]. Exercise train- ing improves body composition, cardiovascular, and metabolic outcomes in people with MetS [6]. High vol- ume of physical activity is associated with lower rates of CVD events, glycosylated hemoglobin (HbA1C %), and systolic blood pressure in older adults [7]. However, universal agreement on the most effective exercise pre- scription to improve MetS for patients with MI remains unclear. Recent studies have demonstrated that high- intensity interval training (HIIT) may ameliorate MetS in obese adults [8], optimize HbA1C in patients with type II diabetes [9], and improve cardiac function in MI patients [10], more so than moderate-intensity continu- ous training (MICT) [8, 10]. However, the impact of HIIT on MetS in patients with MI undergoing early outpatient cardiac rehabilitation (CR) has not been studied. The purpose of this study was to examine the effect of supervised HIIT on MetS presence and severity, and body composition in patients with MI undergoing early outpatient CR. We hypothesized that HIIT will be associ- ated with greater improvements in MetS and body com- position compared to MICT. Methods Design and participants This was a retrospective cohort study of 391 consecutive MI patients enrolled in early outpatient cardiac reha- bilitation (CR) at Mayo Clinic, Rochester, MN between September 1st, 2015 and February 28th, 2018. Of 391 patients, 174 MI patients presented with MetS. Patients meeting the following inclusion criteria were included: (1) diagnosed with both MI and MetS, (2) completion of 36 sessions of supervised outpatient cardiac rehabilita- tion, (3) pre- and post-CR blood lipids and fasting blood glucose tests, and (4) completed pre- and post-CR dual energy X-ray absorptiometry. The cardiac rehabilitation program at Mayo Clinic is a multidisciplinary health care program that includes a highly supervised exercise program (36 exercise sessions), patient education and wellness programs, nutrition and smoking cessation counseling, stress management, and psychological and pharmacological counseling. A standard 36 sessions of CR usually lasts 12 weeks (three sessions per week). Of the 56 eligible patients who met all the inclusion criteria, 42 engaged in HIIT and 14 in MICT (Fig. 1). All aspects of this study conformed to the principles outlined in the Declaration of Helsinki and were approved by the Mayo Clinic Institutional Review Board. All participants agreed to use of their medical records for research purposes. HIIT and MICT protocols Patients performed an average of three supervised HIIT or MICT sessions/week on a treadmill, cycle ergom- eter, or recumbent stepper in the CR center and were prescribed 3  days of self-guided exercise at home. In the 1st week, all patients performed MICT, after that, if patients were able to exercise for ≥  20 min at a rat- ing of perceived exertion (RPE: Borg 6–20) of 12–14, they self-determined to continue MICT or transition to HIIT. The HIIT sessions were characterized by brief, intermittent bouts of high-intensity exercise inter- spersed with periods of low-intensity exercise (active recovery). Because most patients are prescribed heart rate modulating pharmacotherapy after MI and to maximize generalizability and real-world applicability, the intensity of HIIT was prescribed using RPE. These patients began with four high-intensity intervals of 30–60 s at an RPE of 15–17 interspersed with 1–5 min of low-intensity intervals at an RPE  <  14, progress- ing to 5–8 high-intensity intervals of 2–4  min during 20–45 min of training according to the American Col- lege of Sports Medicine (ACSM) guidelines [11]. HIIT was performed only during supervised sessions with frequency not exceeding 3 days/week (non-consecutive days). MICT was performed for 20–45 min at an RPE of 12–14. Heart rate (HR) and rhythm were continu- ously monitored via a 3-lead electrocardiogram (Q-Tel telemonitoring system, Welch Allyn, USA) with blood pressure (systolic [SBP] and diastolic [DBP]) meas- ured by manual sphygmomanometry. Heart rate (HR) data were retrieved from the exercise session report of each patient, which provided documentation on HRs at specific time-points including: (a) before and after each exercise training session for both HIIT and MICT groups, (b) at the end of the second and third intervals for HIIT, and (c) at the mid-point and end of exercise for MICT. Average HR was calculated by averaging HR values that were documented during exercise. The average metabolic equivalent (MET) and exercise time for each exercise session were reported by the Q-Tel telemonitoring system and documented in exercise Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 3. Page 3 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 session reports. Energy expenditure (EE) was calculated according to the equation: calories  = [METs × body weight in kilograms  × 3.5]/200 ×  exercise time, as described previously [12]. Metabolic syndrome criteria The definition of metabolic syndrome (MetS) is based on the revised National Cholesterol Education Program’s Adult Treatment Panel III (ATP III) [1]. An ATP III MetS score was calculated as the sum of the ATP III MetS cri- teria at baseline and completion of CR. Metabolic syndrome z‑score Metabolic syndrome z-score is a continuous score of each MetS variable defined by ATP III, and was calculated from modified z-scores of the following variables: [13] waist circumference; SBP; DBP; triglycerides (TG); fast- ing blood glucose (FBG); ATP III criteria, and standard deviations (denominator of each factor in the formula) using baseline data from the entire study cohort (N = 56): Metabolic syndrome z-score  = [(50-HDL)/9.9] + [(TG- 150)/69.8] + [(FBG-100)/24.5] + [(WC-88)/10.3] + [(SBP- 130)/16.0] + [(DBP-85)/11.2]. Anthropometric measurement Dual-energy X-ray absorptiometry (Lunar iDXA Series X, Madison, WI, USA) was conducted by trained radi- ology technicians using standardized procedures as described previously [14]. The scans were performed within 1 week prior to starting and 1 week after comple- tion of CR. Scans were used to measure total body mass, body fat mass, body lean mass, body fat percentage, and abdominal region fat percentage (the area between the ribs and pelvis). Percentages of the total were calculated accordingly. The scanner was calibrated daily against a manufacturer supplied standard calibration block to control for possible baseline drift. Height was measured using a stadiometer. Dietary assessment Dietary assessment was performed using the Rate-Your- Plate (RYP) questionnaire as previously described [15] during the first and last CR session. Statin therapy intensity assessment Due to the known influence of statin therapy on blood lipids and body composition, we retrieved and analyzed statin therapy intensity data for each patient. Statin Fig. 1  Study enrollment. HIIT high-intensity interval training, MICT moderate-intensity continuous training, DXA dual-energy X-ray absorptiometry Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 4. Page 4 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 therapy intensity was assessed within 1 week prior to the start and within 1 week after the completion of CR and stratified using ACC/AHA guidelines [16]. Statin inten- sity therapy is defined as a pseudo-continuous variable, 3 =  high intensity, 2  =  moderate intensity, 1  = low inten- sity, and 0 = none. Exercise capacity Exercise capacity was evaluated at the beginning and completion of 36 sessions of CR via standard exer- cise stress test, cardiopulmonary exercise test (CPET) or 6 min walk test (6 MWT). The protocols of pre- and post-intervention were the same for each patient. In the present study, exercise capacity was represented as peak oxygen consumed ­ (VO2peak, ml/kg/min) that was directly measured by performing CPET (HIIT  = 28; MICT =  9), the ­ VO2peak calculated by the equation ­VO2peak = 3.5  ml/kg/min * peak metabolic equivalents (METs) that was determined by standard exercise stress test (HIIT  = 8; MICT =  3), or the ­ VO2peak calculated from the equation ­ VO2peak = 4.9486 + 0.023 * walk dis- tance (meters) that was determined via using 6 MWT (HIIT = 6; MICT = 2) as described previously [17]. Depressive symptoms assessment To determine if there was a difference in HIIT- and MICT-induced psychological response, we retrieved Patient Health Questionnaire 9 (PHQ-9) data that was collected monthly for patients to assess patient’s depres- sive symptoms. The PHQ-9 test was conducted as described previously [18]. Statistical analysis The primary outcomes of this study were the mean dif- ferences in metabolic syndrome variables from baseline through 36 sessions of CR between groups. A second- ary outcome of interest was the mean difference in body composition, including total body fat mass, body fat per- centage, abdominal fat percentage, and body lean mass between groups. Baseline data are presented as frequency and percent- age for categorical variables and compared between groups using the Pearson Chi-square test or Fisher exact test. Continuous data are presented as mean and stand- ard deviation and compared between groups using two- sample t-test or non-parametric Wilcoxon rank-sum test, as appropriate depending on the distribution. Prior to analyses, normality was evaluated and the distribu- tion of changes looked approximately normal. Analysis of covariance (ANCOVA) was used to compare the change in each parameter of interest between groups. In this analysis, change was modeled as the outcome in a lin- ear regression model and group effects were tested with adjustment for the baseline value of the parameter being tested. These analyses were repeated in a matched sub- set of each group to control for potential differences in exercise duration, exercise intensity, and exercise energy expenditure. In order to assess differences over time between groups, a repeated measures analysis of variance (ANOVA) was used. In this analysis, measurements at each week were used to examine the interaction of time and group and tested the differences in effects over time between groups. Energy expenditure and METs were log transformed in these analyses to approximate normality prior to analysis. Means and confidence intervals were back-transformed to the original scale for presentation. Comparisons at each week used the method of Scheffe to adjust P-values for multiple comparisons. SAS version 9.4 (Cary, NC) was used for analyses and Two-sided P-val- ues ≤ .05 were considered to be statistically significant. Results Study patients Baseline characteristics were not different between groups (Table 1): age (69  ±  14 vs. 68  ± 10 years P = .78), female (36% vs. 36%, P > .99), body weight (91.2 ± 14.4 vs. 91.5 ± 16.3  kg P =  .95), height (170  ±  10 vs. 171  ± 9  cm P = .84), and BMI (31.5 ± 4.2 vs. 31.3 ± 4.7 kg/m2 P = .90). Comorbidities and medications were also not different between groups (P > .05). Percentage of PCI (50% vs. 57%) and CABG (14% vs. 14%) were not different between groups (P = .64, P > .99 respectively). Twenty-five patients suffered one-vessel disease (MICT  =  6, 42%; HIIT  = 17, 40%; P =  .88), 17 patients suffered two-vessel disease (MICT =  4, 29%; HIIT  = 12, 31%; P =  .99), 14 patients suffered three-vessel disease (MICT = 4, 29%; HIIT = 13, 31%; P =  .74). The number of days between patients’ MI event and the beginning of CR was also not differ- ent between groups (14  ±  4 vs. 14  ± 11  days, P = .34). The ­VO2peak at baseline was not significantly differ- ent between groups (23.7  ±  7.1 vs. 23.0  ± 6.3 ml/kg/min, P = .73). Exercise parameters over the course of cardiac rehabilitation The HIIT group demonstrated significantly higher aver- age HR, average exercise intensity, longer duration of exercise, and higher energy expenditure per session at each time point compared to MICT group (P < .05), while the average exercise intensity (P = .40), duration of exer- cise at 12-weeks (P =  .39), and energy expenditure at 2-weeks (P = .09) and 12-weeks (P = .37) were not differ- ent between groups. Further, there were no differences between groups in average HR (P = .81), average exercise intensity (P =  .40), duration of exercise (P = .68), energy Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 5. Page 5 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 expenditure per session (P = .37) across groups over time (Fig. 2). Dietary quality and depressive symptoms assessment The baseline RYP scores in MICT and HIIT were not different (56  ±  7 vs. 56  ± 7, P =  .99). The changes in RYP scores between groups were not different from base- line to the completion of 36 CR sessions (5 ± 5 vs. 5 ± 5, P = .46). The changes in PHQ-9 scores were not different across the groups after the completion of 36 CR sessions (− 1.2 ± 3.6 vs. − 1.6 ± 3.5, P = .45). Statin therapy intensity assessment All 56 patients were taking statin therapy at baseline. The changes in average statin therapy intensities between the groups were not different from baseline to the comple- tion of 36 CR sessions (0.1 ± 0.3 vs. − 0.1 ± 0.5, P = .30). Metabolic syndrome Compared to MICT, the HIIT group demonstrated greater reductions in MetS presence (relative risk  = 0.5, 95% confidence interval 0.33–0.75, P < .001), MetS z-score (− 3.6 ± 2.9 vs. − 0.8 ± 3.8, P < .001), ATP III MetS scores (P =  .005) and improvements in individual MetS variables, including, waist circumference (P = .01), FBG (P < .001), TG (P = .001) and DBP (P = .001). The changes in HDL-C and SBP were not different between groups (Table 2). Body composition The HIIT group demonstrated greater improvements in total body fat mass (P =  .002), body fat percentage (P = .002), abdominal fat percentage (P = .004), and body lean mass (P = .01) compared to MICT (Fig. 3). Sub‑group analysis Due to the difference in exercise energy expenditure between HIIT and MICT, we matched HIIT and MICT participants for exercise energy expenditure. In this sub- group analysis, the HIIT group demonstrated greater improvements in MetS z-score (P <  .001), ATP III MetS score (P =  .005), and MetS variables (including FBG (P =  .002), TG (P =  .008), DBP (P <  .001), total body fat mass (P =  .02), body fat percentage (P =  .01), body lean mass (P =  .03), and abdominal fat percentage (P = .01) compared to MICT, with no differences in RYP scores (P =  .95) and average statin therapy intensity between groups from baseline to follow-up (P = .23) (Table 3). Discussion This study has, for the first time, demonstrated that supervised HIIT elicited greater improvements in MetS z-score and ATP III MetS score, and some components of MetS that include waist circumference, FBG, TG, and DBP, than MICT in MI patients with MetS enrolled in early outpatient CR. These findings support the use of HIIT, as an alternative and/or complimentary to MICT, for MI patients with MetS to improve CVD risk factor related outcomes. Our findings demonstrate that HIIT decreased the prevalence of MetS and MetS severity (MetS z-score) to a greater extent than MICT in MI patients enrolled in early outpatient CR. The observed magnitude of HIIT-induced benefit in the current study parallels a recent study by Morales-Palomo et al. [19] in individuals with MetS but without MI. These authors found that 2 yearly 16-week HIIT programs resulted in chronically lower MetS and halted the increase in medication use that occurs in Table 1  Baseline characteristics of study patients ACEIs angiotensin-converting enzyme inhibitors, ARBs angiotensin II receptor blockers, BMI body mass index, CABG coronary artery bypass graft, CCBs calcium channel blockers, HIIT high-intensity interval training, MICT moderate-intensity continuous training, PCI percutaneous coronary intervention, VO2peak peak oxygen consumed MICT (n = 14) HIIT (n = 42) P value Age, mean (SD), years 69 ± 14 68 ± 10 P = .78 Female sex, n (%) 5 (36) 15 (36) P > .99 Height, mean (SD), cm 170 ± 10 171 ± 9 P = .84 Body weight, mean (SD), kg 91.2 ± 14.4 91.5 ± 16.3 P = .95 BMI, mean (SD), kg/m2 31.5 ± 4.2 31.3 ± 4.7 P = .90 Days between CR and MI, mean (SD), days 14 ± 4 14 ± 11 P = .34 Medical history, n (%)  PCI 7 (50) 24 (57) P = .64  CABG 2 (14) 6 (14) P > .99  Hyperglycemia 11 (79) 33 (79) P > .99  Hypertension 8 (57) 20 (48) P = .54  Dyslipidemia 14 (100) 39 (92) P = .57  Ever smoker 5 (36) 14 (33) P > .99 Coronary angiography  One-vessel disease, n (%) 6 (42) 17 (40) P = .88  Two-vessel disease, n (%) 4 (29) 12 (29) P = .99  Three-vessel disease, n (%) 4 (29) 13 (31) P = .74 Medications, n (%)  Insulin 3 (21) 9 (21) P > .99  Oral hypoglycemic drugs 4 (29) 15 (36) P = .75  Statins 14 (100) 42 (100) P = .99  ACEIs/ARBs 9 (64) 24 (57) P = .64  Antiplatelet drugs 12 (86) 41 (98) P = .15  Anticoagulants 7 (50) 26 (62) P = .43  Beta receptor blockers 9 (64) 37 (88) P = .10  CCBs 2 (14) 7 (17) P > .99  Diuretics 2 (14) 1 (2) P = .15  Nitrates 4 (29) 6 (14) P = .25 Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 6. Page 6 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 non-exercising MetS individuals. Similarly, Ramos et al. [8] demonstrated low-volume HIIT was sufficient to ameliorate the MetS severity in middle-aged adults, and was superior to MICT in terms of time efficiency. In addition, an across race study demonstrated that high- intensity interval and resistance training led to improve- ments in cardiometabolic risk factors, including FBG, TG, and SBP, in both Mapuche and European hyper- glycemic adult women [20]. Our findings are consistent with these observations further supporting the important impact of HIIT on components of MetS and suggest that HIIT could be encouraged for MI patient with MetS. The present study, for the first time, demonstrated that HIIT contributes to greater decreases in total body fat mass (P =  .002), body fat percentage (P = .002), and abdominal fat percentage (P < .004) while increasing body lean mass (P =  .01) in MI patients with MetS compared to MICT. Several other studies have also examined the efficacy of HIIT on reducing subcutaneous and abdomi- nal fat in overweight adolescents [21] and type 2 diabetic men [22]. Trapp et al. [23] compared HIIT and MICT in young women and found that HIIT resulted in greater reductions in subcutaneous fat. These are important findings, as increasing evidence suggests body fat (and its distribution) and lean body mass are associated with risk of incident MetS [24, 25]. For example, risk of MetS for individuals in the highest abdominal fat quintile is more than three times greater compared with the lowest quintile [25]. Moreover, individuals with high fat and low muscle mass have an approximately twofold increase in the risk of developing MetS [24]. We have also demon- strated that total body fat mass, abdominal fat percent- age, and body lean mass are independent risk factors for long-term cardiovascular events and mortality in patients Fig. 2  Exercise parameters over the course of cardiac rehabilitation. HIIT high-intensity interval training, MICT moderate-intensity continuous training. a Average heart rate during training. HIIT vs. MICT, 2-weeks: 110 vs. 96 bpm, P = .04; 4-weeks: 113 vs. 96 bpm, P = .008; 8-weeks: 116 vs. 98 bpm, P = .009; 12-weeks: 116 vs. 102 bpm, P = .003, respectively. There was no evidence of a difference across groups over time (P = .81). b Average intensity. 2-weeks: 3.2 vs. 2.6 METs, P = .01; 4-weeks: 3.3 vs. 2.5 METs, P = .01; 8-weeks: 3.5 vs. 2.9 METs, P = .02; 12-weeks: 3.8 vs. 3.2 METs, P = .03, respectively. Evidence of a difference across groups over time was noted (P = .40). c Duration of exercise. 2-weeks: 31 vs. 25 min, P = .03; 4-weeks: 33 vs. 27 min, P = .008; 8-weeks: 35 vs. 27 min, P = .007; 12-weeks: 34 vs. 30 min, P = .39, respectively. There was no evidence of a difference across groups over time (P = .68). d Energy expenditure per session. 2-weeks: 143 vs. 98 kcal, P = .09; 4-weeks: 152 vs. 100 kcal, P = .01; 8-weeks: 161 vs. 124 kcal, P = .05; 12-weeks: 163 vs. 143 kcal, P = .41, respectively. There was no evidence of a difference across groups over time (P = .37). Results presented are mean and 95% confidence limits based on repeated measures ANOVA. Comparisons at each time point are adjusted for multiple comparisons using the method of Scheffe Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 7. Page 7 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 Table 2  Outcomes BMI body mass index, CR cardiac rehabilitation, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-c high-density lipoprotein cholesterol, HIIT high-intensity interval training, MetS metabolic syndrome, MICT moderate-intensity continuous training, Peak VO2 peak oxygen consumed, PHQ-9 patient health questionnaire 9, SBP systolic blood pressure, TG triglycerides MICT (n = 14) HIIT (n = 42) ANCOVA Baseline Change Baseline Change P-value Rate-Your-Plate 56 ± 7 5 ± 5 56 ± 7 5 ± 5 P = .46 Average statin 2.4 ± 0.7 0.1 ± 0.3 2.8 ± 0.5 − 0.1 ± 0.5 P = .30 MetS variables  MetS z-score 5.7 ± 3.6 − 0.8 ± 3.8 4.6 ± 3.4 − 3.6 ± 2.9 P < .001  ATP III MetS score 3.9 ± 0.7 − 0.6 ± 1.0 3.6 ± 0.6 − 1.2 ± 1.0 P = .005  Waist circumference, cm 110 ± 11 1 ± 5 110 ± 10 − 3 ± 5 P = .01  FBG, mg/dl 130.4 ± 38.7 − 3.9 ± 25.8 129.3 ± 37.3 − 25.8 ± 34.8 P < .001  TG, mg/dl 222.5 ± 80.1 − 10.4 ± 105.3 185.5 ± 101.5 − 67.8 ± 86.7 P < .001  HDL-c, mg/dl 38.9 ± 10.8 6.4 ± 8.3 40.3 ± 9.8 3.8 ± 9.0 P = .42  SBP, mmHg 122 ± 18 0 ± 25 122 ± 15 − 6 ± 18 P = .16  DBP, mmHg 71 ± 12 0 ± 13 68 ± 11 − 7 ± 11 P = .001 Body composition  Body weight, kg 91.2 ± 14.4 0.6 ± 4.8 91.5 ± 16.3 − 0.5 ± 4.9 P = .45  BMI, kg/m2 31.5 ± 4.2 0 ± 1.5 31.3 ± 4.7 − 0.1 ± 1.7 P = .83  Fat mass, kg 35.4 ± 6.6 0 ± 2.2 35.7 ± 8.5 − 2.1 ± 2.1 P = .002  Body fat, % 40.2 ± 4.9 − 0.2 ± 1.4 39.9 ± 5.9 − 1.8 ± 1.7 P = .002  Lean mass, kg 53.5 ± 9.3 − 0.9 ± 3.2 53.5 ± 9.8 0.9 ± 1.9 P = .01  Abdominal fat, % 47.5 ± 5.2 0.1 ± 2.4 49.6 ± 5.7 − 2.2 ± 2.6 P = .004   Peak ­VO2, ml/kg/min 23.7 ± 7.1 1.4 ± 0.9 23.0 ± 6.3 5.0 ± 2.5 P = .03  PHQ-9 4.0 ± 2.1 − 1.2 ± 3.6 4.0 ± 3.2 − 1.6 ± 3.5 P = .45 Fig. 3  Changes in metabolic syndrome and body composition variables from the baseline to the completion of 36 sessions of cardiac rehabilitation across MICT and HIIT groups. ATP III National Cholesterol Education Program’s Adult Treatment Panel III, HIIT high-intensity interval training, MetS metabolic syndrome, MICT moderate-intensity continuous training. Values are reported as mean ± standard deviation Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 8. Page 8 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 with [26, 27] and without coronary heart disease (CHD) [28]. In patients with CHD in the highest quartile of body fat percentage, risk of cardiovascular events is double compared to the lowest quartile [27]. In contrast, two recent studies by Keating et  al. [29] and Wewege et  al. [30] demonstrated that HIIT and MICT elicited similar benefits for improvement in body composition for over- weight and obese adults, especially once controlled for energy expenditure. Our findings combined with others support that HIIT may provide similar or enhanced ben- efits for risk factor management and should be viewed as an important treatment strategy for MI patients with MetS. This study showed that there were no changes in body mass and BMI in either MICT or HIIT groups, which are consistent with previous studies by Keating et al. [29] and Wewege et al. [30] that demonstrated that HIIT and MICT elicit similar changes in body mass. This phenom- enon may be related to the obesity paradox. Overweight and obesity are associated with an increased likelihood of developing cardiovascular disease and all-cause mortal- ity [31] and have become increasingly common world- wide, with overweight and obesity conventionally defined as a BMI of >  25 kg/m2 and >  30 kg/m2 , respectively. In contrast to the general population, patients with CHD demonstrate an inverse relationship between BMI and mortality, termed the obesity paradox [32]. However, it is now apparent that this paradox is related to the preser- vation of lean muscle mass as there is no paradox in the general population [33] or patients with CHD [27] when measuring body fat percentage instead of BMI. This point helps to understand how MetS parameters were improved in our HIIT patients, even in the absence of BMI changes. A variety of HIIT protocols have been developed and used for CHD patients [34], which vary in intensity, inter- val duration, and the number of intervals. Further, exer- cise intensity is generally prescribed using a percent of maximal oxygen consumption, percent of maximal heart rate, percent of maximal power, or RPE (rated perceived exertion, Borg scale) [34, 35]. The present study used RPE to prescribe the intensity of exercise with accompany- ing HR monitoring. HIIT prescribed using RPE has been used across the aging spectrum [36, 37]. Buchheit et al. [38] and Levinger et al. [39] demonstrated that the RPE has shown a great correlation with HR, ventilation, and ­VO2 in individuals both with and without CAD, and the correlation is not impacted by beta-blocker medication, a commonly used HR modulating medication by patients with MI [39]. In addition, HIIT prescribed by RPE can promote greater positive responses than both HIIT and MICT when prescribed with imposed intensity, such as workload and HR, due to the perceived autonomy, time efficiency, and changing stimulus [36]. The present study Table 3  Outcomes after matching for differences in exercise energy expenditure BMI body mass index, CR cardiac rehabilitation, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-c high-density lipoprotein cholesterol, HIIT high-intensity interval training, MetS metabolic syndrome, MICT moderate-intensity continuous training, SBP systolic blood pressure, TG triglycerides MICT (n = 14) HIIT (n = 14) ANCOVA Baseline Change Baseline Change P-value Rate-Your-Plate 56 ± 7 5 ± 5 55 ± 7 5 ± 7 P = .95 Average statin 2.4 ± 0.7 0.1 ± 0.3 2.6 ± 0.7 − 0.1 ± 0.3 P = .23 MetS variables  MetS z-score 5.7 ± 3.6 − 0.8 ± 3.8 5.6 ± 3.2 − 5.3 ± 3.0 P < .001  ATP III MetS score 4 ± 1 − 1 ± 1 4 ± 0 − 2 ± 1 P = .005  Waist circumference, cm 110 ± 11 1 ± 5 103 ± 9 − 0.4 ± 2.2 P = .31  FBG, mg/dl 130.4 ± 38.7 − 3.9 ± 25.8 138.9 ± 46.6 − 40.1 ± 46.6 P = .002  TG, mg/dl 222.5 ± 80.1 − 10.4 ± 105.3 232.0 ± 111.1 − 97.2 ± 105.7 P = .008  HDL-c, mg/dl 38.9 ± 10.8 6.4 ± 8.3 37.6 ± 7.3 3.7 ± 4.8 P = .26  SBP, mmHg 122 ± 18 0 ± 25 122 ± 15 − 13 ± 12 P = .13  DBP, mmHg 71 ± 12 0 ± 13 70 ± 7 − 12 ± 8 P < .001 Body composition  Body weight, kg 91.2 ± 14.4 0.6 ± 4.8 80.3 ± 13.2 1.4 ± 7.0 P = .72  BMI, kg/m2 31.5 ± 4.2 − 0.1 ± 1.5 28.6 ± 4.5 0.7 ± 2.4 P = .92  Fat mass, kg 35.4 ± 6.6 0 ± 2.2 30.9 ± 7.6 − 1.7 ± 1.8 P = .02  Body fat, % 40.2 ± 4.9 − 0.2 ± 1.4 38.8 ± 7.5 − 1.8 ± 1.7 P = .01  Lean mass, kg 53.5 ± 9.3 − 0.9 ± 3.2 48.5 ± 8.5 1.2 ± 1.4 P = .03  Abdominal fat, % 47.5 ± 5.2 0.1 ± 2.4 48.1 ± 7.4 − 2.4 ± 2.4 P = .01 Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 9. Page 9 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 demonstrates that RPE should be considered an appro- priate alternative or supplementary method to HR for prescribing exercise intensity for HIIT in MI patients with MetS. To determine the relation of energy intake, statin ther- apy intensity, and energy expenditure (EE) during exer- cise and HIIT-induced improvements in MetS and body composition, the present study assessed dietary quality, average statin therapy intensity and the EE per exercise session over the course of 36 sessions of CR. Our results showed that there were no differences in RYP scores (die- tary quality) and statin therapy intensity across groups from baseline to follow-up compared to MICT. Addi- tionally, HIIT induced similar exercise EEs to MICT at the beginning and end of 36 CR sessions. These findings suggest that energy intake, statin therapy intensity, and EE during exercise are not primary explanations for the HIIT-induced greater improvements in MetS and body composition than MICT in these patients. To confirm the accuracy of these findings, we matched a sub-group of HIIT and MICT patients on exercise EE specifically and found that the improvements in MetS and body composi- tion in the HIIT group persisted. The exact mechanisms whereby HIIT leads to greater improvements in MetS variables and body composition in MI patients with MetS remain unclear. The mecha- nisms may involve a wide range of systems responsible for the physiologic adaptations to structured exercise, including the cardiovascular system, respiratory system, and musculoskeletal systems. Increasing evidence sug- gests that HIIT can improve post-infarction left ventricu- lar remodeling [40], augment stroke volume in patients with type 2 diabetes [41], optimize heart rate recovery after exercise in MI patients [42], and improve brachial artery flow-mediated dilation in sedentary adults [43] and type 2 diabetes [44, 45], which together may con- tribute to the improvements in insulin sensitivity, blood pressure, and body composition [46]. With regards to the respiratory system, respiratory muscle dysfunction is a common manifestation in older patients with CVD [47], Tasoulis et al. demonstrated that 12 weeks of HIIT sig- nificantly improved respiratory muscle function in older adults with HF [48]. With respect to skeletal muscle, we have previously shown that 4-weeks of aerobic exercise can enhance skeletal muscle mitochondrial biogenesis and function in male mice [49]. Motta et  al. [50] also showed that HIIT ameliorated fructose-induced meta- bolic dysfunction in male mice through mitochondrial biogenesis and β-oxidation, via irisin and PGC1 α in skel- etal muscle. Moreover, several recent trials have demon- strated that 3–12 weeks of HIIT can significantly increase resting metabolic rate [51] and post-exercise oxygen consumption in healthy adults [52], and fat oxidation in obese adolescents [53]. In summary, HIIT can elicit numerous improvements in organ structure and physi- ological functions of multiple systems; however, more research is warranted to better understand the primary mechanisms of HIIT-induced cardiometabolic benefits. With respect to the safety of performing HIIT, all par- ticipants enrolled in this study completed 36 sessions of CR without a single major adverse event. Although no major adverse events were registered, the current study was not designed/powered to demonstrate safety of HIIT in patients with MI. However, the safety of supervised HIIT in CR is generally well documented in patients with established coronary artery disease [54, 55]. Study limitations It is important to recognize the retrospective, obser- vational nature of the present study design. Additional research in this area is encouraged to confirm these findings in a prospective fashion. To avoid bias associ- ated with the number of HIIT sessions completed, we only enrolled the patients who completed the standard 36 sessions of outpatient CR and attended follow-up assessments, which may have introduced selection bias. The patients in this study are overweight; therefore, additional research focusing on MI patients with MetS within “normal weight” is encouraged. Furthermore, although not unusual in similar studies, an unintended consequence of our clinical population is that only 36% were women. Thus, additional studies may be needed to ensure the generalizability of our findings. Conclusions The present study demonstrates that supervised HIIT prescribed by RPE can elicit greater improvements in MetS and body composition for MI patients with MetS compared to MICT. These findings support the use of HIIT as a treatment tool to improve MetS compo- nents in MI patients enrolled in early outpatient cardiac rehabilitation. Abbreviations MetS: metabolic syndrome; MI: myocardial infarction; HIIT: high-intensity interval training; MICT: moderate-intensity continuous training; CR: cardiac rehabilitation; DXA: dual-energy x-ray absorptiometry; RPE: rating of perceived exertion; ACSM: American College of Sports Medicine; HR: heart rate; SBP: systolic blood pressure; DBP: diastolic blood pressure; ATP III: Adult Treat‑ ment Panel III; TG: triglycerides; FBG: fasting blood glucose; HDL: high density lipoprotein; RYP: rate your plate; CPET: cardiopulmonary exercise test; 6 MWT: 6 min walk test; VO2peak: maximal oxygen consumption; ANCOVA: analysis of covariance; ANOVA: analysis of variance; CHD: coronary heart disease; EE: energy expenditure. Acknowledgements We thank the patients and staff of Mayo Clinic Cardiac Rehabilitation Program, in Rochester, MN, for their valuable contributions to the study. Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 10. Page 10 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 Authors’contributions YD, RJT, TPO, RWS and SL are responsible for the conception and design of the work. YD, TPO, JRM, HH, ARB, JRS and SL contributed to the acquisition or inter‑ pretation of the work. YD and TPO drafted the manuscript. All authors critically revised the manuscript, gave final approval and agree to be accountable for all aspects of the work ensuring integrity and accuracy. All authors read and approved the final manuscript. Funding The present study was supported in part by grants from the National Institutes of Health (HL-126638 to TPO) and Hunan Development and Reform Commis‑ sion Foundation of China (Grant no. [2012] 1521 to SL). Availability of data and materials Not applicable. Ethics approval and consent to participate Approval was received from the Mayo Clinic Institutional Review Board and authorization for the usage of medical records was obtained. Consent for publication It was obtained through authorization of the use of medical records by the patients. Competing interests The authors declare that they have no competing interests. Received: 14 May 2019 Accepted: 7 August 2019 References 1. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, Gordon DJ, Krauss RM, Savage PJ, Smith SC Jr, et al. Diagnosis and man‑ agement of the metabolic syndrome: an American Heart Association/ National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112(17):2735–52. 2. Hu H, Nakagawa T, Honda T, Yamamoto S, Nanri A, Konishi M, Okazaki H, Kuwahara K, Hori A, Nishiura C, et al. Metabolic syndrome over 4 years before the onset of cardiovascular disease-nested case–control study. Circ J. 2018;82(2):430–6. 3. Cavallari I, Cannon CP, Braunwald E, Goodrich EL, Im K, Lukas MA, O’Donoghue ML. Metabolic syndrome and the risk of adverse cardio‑ vascular events after an acute coronary syndrome. Eur J Prev Cardiol. 2018;25(8):830–8. 4. Han TS, Lean ME. A clinical perspective of obesity, metabolic syndrome and cardiovascular disease. JRSM Cardiovasc Dis. 2016;5:2048004016633371. 5. Fihn SD, Gardin JM, Abrams J, Berra K, Blankenship JC, Dallas AP, Douglas PS, Foody JM, Gerber TC, Hinderliter AL, et al. 2012 ACCF/AHA/ACP/AATS/ PCNA/SCAI/STS guideline for the diagnosis and management of patients with stable ischemic heart disease: a report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines, and the American College of Physicians, American Association for Thoracic Surgery, Preventive Cardiovascular Nurses Asso‑ ciation, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons. Circulation. 2012;126(25):e354–471. 6. Ostman C, Smart NA, Morcos D, Duller A, Ridley W, Jewiss D. The effect of exercise training on clinical outcomes in patients with the metabolic syndrome: a systematic review and meta-analysis. Cardiovasc Diabetol. 2017;16(1):110. 7. Amadid H, Johansen NB, Bjerregaard AL, Brage S, Faerch K, Lauritzen T, Witte DR, Sandbaek A, Jorgensen ME, Vistisen D. The role of physical activ‑ ity in the development of first cardiovascular disease event: a tree-struc‑ tured survival analysis of the Danish ADDITION-PRO cohort. Cardiovasc Diabetol. 2018;17(1):126. 8. Ramos JS, Dalleck LC, Borrani F, Beetham KS, Wallen MP, Mallard AR, Clark B, Gomersall S, Keating SE, Fassett RG, et al. Low-volume high-intensity interval training is sufficient to ameliorate the severity of metabolic syndrome. Metab Syndr Relat Disord. 2017;15(7):319–28. 9. Grace A, Chan E, Giallauria F, Graham PL, Smart NA. Clinical outcomes and glycaemic responses to different aerobic exercise training intensities in type II diabetes: a systematic review and meta-analysis. Cardiovasc Diabetol. 2017;16(1):37. 10. Choi HY, Han HJ, Choi JW, Jung HY, Joa KL. Superior effects of high-inten‑ sity interval training compared to conventional therapy on cardiovascular and psychological aspects in myocardial infarction. Ann Rehabil Med. 2018;42(1):145–53. 11. Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM, Nieman DC, Swain DP, American College of Sports Medicine position stand. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc. 2011;43(7):1334–59. 12. Ainsworth BE, Haskell WL, Herrmann SD, Meckes N, Bassett DR Jr, Tudor- Locke C, Greer JL, Vezina J, Whitt-Glover MC, Leon AS. 2011 compendium of physical activities: a second update of codes and MET values. Med Sci Sports Exerc. 2011;43(8):1575–81. 13. Dieli-Conwright CM, Courneya KS, Demark-Wahnefried W, Sami N, Lee K, Buchanan TA, Spicer DV, Tripathy D, Bernstein L, Mortimer JE. Effects of aerobic and resistance exercise on metabolic syndrome, sarcopenic obe‑ sity, and circulating biomarkers in overweight or obese survivors of breast cancer: a randomized controlled trial. J Clin Oncol. 2018;36(9):875–83. 14. Imboden MT, Welch WA, Swartz AM, Montoye AH, Finch HW, Harber MP, Kaminsky LA. Reference standards for body fat measures using GE dual energy x-ray absorptiometry in Caucasian adults. PLoS ONE. 2017;12(4):e0175110. 15. Gans KM, Hixson ML, Eaton CB, Lasater TM. Rate your plate: a dietary assessment and educational tool for blood cholesterol control. Nutr Clin Care. 2000;3(3):163–9. 16. Stone NJ, Robinson JG, Lichtenstein AH, Bairey Merz CN, Blum CB, Eckel RH, Goldberg AC, Gordon D, Levy D, Lloyd-Jones DM, et al. 2013 ACC/ AHA guideline on the treatment of blood cholesterol to reduce athero‑ sclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014;63(25 Pt B):2889–934. 17. Ross RM, Murthy JN, Wollak ID, Jackson AS. The six minute walk test accu‑ rately estimates mean peak oxygen uptake. BMC Pulm Med. 2010;10:31. 18. Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001;16(9):606–13. 19. Morales-Palomo F, Ramirez-Jimenez M, Ortega JF, Mora-Rodriguez R. Exercise periodization over the year improves metabolic syndrome and medication use. Med Sci Sports Exerc. 2018;50(10):1983–91. 20. Alvarez C, Ramirez-Velez R, Ramirez-Campillo R, Lucia A, Alonso-Martinez AM, Faundez H, Cadore EL, Izquierdo M. Improvements cardiometabolic risk factors in Latin American Amerindians (the Mapuche) with concur‑ rent training. Scand J Med Sci Sports. 2019;29(6):886–96. 21. Tjonna AE, Stolen TO, Bye A, Volden M, Slordahl SA, Odegard R, Skogvoll E, Wisloff U. Aerobic interval training reduces cardiovascular risk factors more than a multitreatment approach in overweight adolescents. Clin Sci. 2009;116(4):317–26. 22. Boudou P, Sobngwi E, Mauvais-Jarvis F, Vexiau P, Gautier JF. Absence of exercise-induced variations in adiponectin levels despite decreased abdominal adiposity and improved insulin sensitivity in type 2 diabetic men. Eur J Endocrinol. 2003;149(5):421–4. 23. Trapp EG, Chisholm DJ, Freund J, Boutcher SH. The effects of high-inten‑ sity intermittent exercise training on fat loss and fasting insulin levels of young women. Int J Obes. 2008;32(4):684–91. 24. Kim K, Park SM. Association of muscle mass and fat mass with insulin resistance and the prevalence of metabolic syndrome in Korean adults: a cross-sectional study. Sci Rep. 2018;8(1):2703. 25. Kwon H, Kim D, Kim JS. Body fat distribution and the risk of incident met‑ abolic syndrome: a longitudinal cohort study. Sci Rep. 2017;7(1):10955. 26. Medina-Inojosa JR, Batsis JA, Supervia M, Somers VK, Thomas RJ, Jenkins S, Grimes C, Lopez-Jimenez F. Relation of waist–hip ratio to long-term car‑ diovascular events in patients with coronary artery disease. Am J Cardiol. 2018;121(8):903–9. 27. Medina-Inojosa JR, Somers VK, Thomas RJ, Jean N, Jenkins SM, Gomez-Ibarra MA, Supervia M, Lopez-Jimenez F. Association between adiposity and lean mass with long-term cardiovascular events in Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 11. Page 11 of 11 Dun et al. Cardiovasc Diabetol (2019) 18:104 • fast, convenient online submission • thorough peer review by experienced researchers in your field • rapid publication on acceptance • support for research data, including large and complex data types • gold Open Access which fosters wider collaboration and increased citations maximum visibility for your research: over 100M website views per year • At BMC, research is always in progress. Learn more biomedcentral.com/submissions Ready to submit your research ? Choose BMC and benefit from: patients with coronary artery disease: no paradox. J Am Heart Assoc. 2018;7(10):e007505. https​://doi.org/10.1161/JAHA.117.00750​7. 28. Padwal R, Leslie WD, Lix LM, Majumdar SR. Relationship among body fat percentage, body mass index, and all-cause mortality: a cohort study. Ann Intern Med. 2016;164(8):532–41. 29. Keating SE, Johnson NA, Mielke GI, Coombes JS. A systematic review and meta-analysis of interval training versus moderate-intensity continuous training on body adiposity. Obes Rev. 2017;18(8):943–64. 30. Wewege M, van den Berg R, Ward RE, Keech A. The effects of high-inten‑ sity interval training vs. moderate-intensity continuous training on body composition in overweight and obese adults: a systematic review and meta-analysis. Obes Rev. 2017;18(6):635–46. 31. Preston SH, Vierboom YC, Stokes A. The role of obesity in excep‑ tionally slow US mortality improvement. Proc Natl Acad Sci USA. 2018;115(5):957–61. 32. Romero-Corral A, Montori VM, Somers VK, Korinek J, Thomas RJ, Allison TG, Mookadam F, Lopez-Jimenez F. Association of bodyweight with total mortality and with cardiovascular events in coronary artery disease: a systematic review of cohort studies. Lancet. 2006;368(9536):666–78. 33. Dong B, Peng Y, Wang Z, Adegbija O, Hu J, Ma J, Ma YH. Joint associa‑ tion between body fat and its distribution with all-cause mortality: a data linkage cohort study based on NHANES (1988–2011). PLoS ONE. 2018;13(2):e0193368. 34. Ribeiro PAB, Boidin M, Juneau M, Nigam A, Gayda M. High-intensity inter‑ val training in patients with coronary heart disease: prescription models and perspectives. Ann Phys Rehabil Med. 2017;60(1):50–7. 35. Dun Y, Smith JR, Liu S, Olson TP. High-intensity interval training in cardiac rehabilitations. Clin Geriatr Med. 2019 (in press). 36. Thum JS, Parsons G, Whittle T, Astorino TA. High-intensity interval training elicits higher enjoyment than moderate intensity continuous exercise. PLoS ONE. 2017;12(1):e0166299. 37. Viana AA, Fernandes B, Alvarez C, Guimaraes GV, Ciolac EG. Prescribing high-intensity interval exercise by RPE in individuals with type 2 diabetes: metabolic and hemodynamic responses. Appl Physiol Nutr Metab. 2019;44(4):348–56. 38. Buchheit M, Laursen PB. High-intensity interval training, solutions to the programming puzzle: part I: cardiopulmonary emphasis. Sports Med. 2013;43(5):313–38. 39. Levinger I, Bronks R, Cody DV, Linton I, Davie A. Perceived exertion as an exercise intensity indicator in chronic heart failure patients on Beta- blockers. J Sports Sci Med. 2004;3(YISI 1):23–7. 40. Godfrey R, Theologou T, Dellegrottaglie S, Binukrishnan S, Wright J, Whyte G, Ellison G. The effect of high-intensity aerobic interval training on postinfarction left ventricular remodelling. BMJ Case Rep. 2013. https​:// doi.org/10.1136/bcr-2012-00766​8. 41. Wilson GA, Wilkins GT, Cotter JD, Lamberts RR, Lal S, Baldi JC. Impaired ventricular filling limits cardiac reserve during submaximal exercise in people with type 2 diabetes. Cardiovasc Diabetol. 2017;16(1):160. 42. Boidin M, Gayda M, Henri C, Hayami D, Trachsel LD, Besnier F, Lalonge J, Juneau M, Nigam A. Effects of interval training on risk markers for arrhythmic death: a randomized controlled trial. Clin Rehabil. 2019;33(8):1320–30. 43. Ramirez-Velez R, Hernandez-Quinones PA, Tordecilla-Sanders A, Alvarez C, Ramirez-Campillo R, Izquierdo M, Correa-Bautista JE, Garcia-Hermoso A, Garcia RG. Effectiveness of HIIT compared to moderate continuous train‑ ing in improving vascular parameters in inactive adults. Lipids Health Dis. 2019;18(1):42. 44. Hollekim-Strand SM, Bjorgaas MR, Albrektsen G, Tjonna AE, Wisloff U, Ingul CB. High-intensity interval exercise effectively improves cardiac function in patients with type 2 diabetes mellitus and dias‑ tolic dysfunction: a randomized controlled trial. J Am Coll Cardiol. 2014;64(16):1758–60. 45. Qiu S, Cai X, Yin H, Sun Z, Zugel M, Steinacker JM, Schumann U. Exercise training and endothelial function in patients with type 2 diabetes: a meta-analysis. Cardiovasc Diabetol. 2018;17(1):64. 46. Campbell WW, Kraus WE, Powell KE, Haskell WL, Janz KF, Jakicic JM, Troiano RP, Sprow K, Torres A, Piercy KL, et al. High-intensity interval training for cardiometabolic disease prevention. Med Sci Sports Exerc. 2019;51(6):1220–6. 47. Verissimo P, Casalaspo TJ, Goncalves LH, Yang AS, Eid RC, Timenetsky KT. High prevalence of respiratory muscle weakness in hospitalized acute heart failure elderly patients. PLoS ONE. 2015;10(2):e0118218. 48. Tasoulis A, Papazachou O, Dimopoulos S, Gerovasili V, Karatzanos E, Kyprianou T, Drakos S, Anastasiou-Nana M, Roussos C, Nanas S. Effects of interval exercise training on respiratory drive in patients with chronic heart failure. Respir Med. 2010;104(10):1557–65. 49. Dun Y, Liu S, Zhang W, Xie M, Qiu L. Exercise combined with Rhodiola sacra supplementation improves exercise capacity and ameliorates exhaustive exercise-induced muscle damage through enhancement of mitochondrial quality control. Oxid Med Cell Longev. 2017;2017:8024857. 50. Motta VF, Bargut TL, Aguila MB, Mandarim-de-Lacerda CA. Treating fructose-induced metabolic changes in mice with high-intensity interval training: insights in the liver, white adipose tissue, and skeletal muscle. J Appl Physiol (1985). 2017;123(4):699–709. 51. Schubert MM, Clarke HE, Seay RF, Spain KK. Impact of 4 weeks of interval training on resting metabolic rate, fitness, and health-related outcomes. Appl Physiol Nutr Metab. 2017;42(10):1073–81. 52. Schleppenbach LN, Ezer AB, Gronemus SA, Widenski KR, Braun SI, Janot JM. Speed- and circuit-based high-intensity interval training on recovery oxygen consumption. Int J Exerc Sci. 2017;10(7):942–53. 53. Lazzer S, Tringali G, Caccavale M, De Micheli R, Abbruzzese L, Sartorio A. Effects of high-intensity interval training on physical capacities and substrate oxidation rate in obese adolescents. J Endocrinol Invest. 2017;40(2):217–26. 54. Authors/Task Force M, Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C, Catapano AL, Cooney MT, Corra U, Cosyns B, et al. 2016 European Guide‑ lines on cardiovascular disease prevention in clinical practice: the Sixth Joint Task Force of the European Society of Cardiology and Other Socie‑ ties on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Atherosclerosis. 2016;252:207–74. 55. Rognmo O, Moholdt T, Bakken H, Hole T, Molstad P, Myhr NE, Grimsmo J, Wisloff U. Cardiovascular risk of high- versus moderate-intensity aerobic exercise in coronary heart disease patients. Circulation. 2012;126(12):1436–40. Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in pub‑ lished maps and institutional affiliations. Content courtesy of Springer Nature, terms of use apply. Rights reserved.
  • 12. 1. 2. 3. 4. 5. 6. Terms and Conditions Springer Nature journal content, brought to you courtesy of Springer Nature Customer Service Center GmbH (“Springer Nature”). Springer Nature supports a reasonable amount of sharing of research papers by authors, subscribers and authorised users (“Users”), for small- scale personal, non-commercial use provided that all copyright, trade and service marks and other proprietary notices are maintained. By accessing, sharing, receiving or otherwise using the Springer Nature journal content you agree to these terms of use (“Terms”). For these purposes, Springer Nature considers academic use (by researchers and students) to be non-commercial. These Terms are supplementary and will apply in addition to any applicable website terms and conditions, a relevant site licence or a personal subscription. These Terms will prevail over any conflict or ambiguity with regards to the relevant terms, a site licence or a personal subscription (to the extent of the conflict or ambiguity only). For Creative Commons-licensed articles, the terms of the Creative Commons license used will apply. We collect and use personal data to provide access to the Springer Nature journal content. We may also use these personal data internally within ResearchGate and Springer Nature and as agreed share it, in an anonymised way, for purposes of tracking, analysis and reporting. We will not otherwise disclose your personal data outside the ResearchGate or the Springer Nature group of companies unless we have your permission as detailed in the Privacy Policy. While Users may use the Springer Nature journal content for small scale, personal non-commercial use, it is important to note that Users may not: use such content for the purpose of providing other users with access on a regular or large scale basis or as a means to circumvent access control; use such content where to do so would be considered a criminal or statutory offence in any jurisdiction, or gives rise to civil liability, or is otherwise unlawful; falsely or misleadingly imply or suggest endorsement, approval , sponsorship, or association unless explicitly agreed to by Springer Nature in writing; use bots or other automated methods to access the content or redirect messages override any security feature or exclusionary protocol; or share the content in order to create substitute for Springer Nature products or services or a systematic database of Springer Nature journal content. In line with the restriction against commercial use, Springer Nature does not permit the creation of a product or service that creates revenue, royalties, rent or income from our content or its inclusion as part of a paid for service or for other commercial gain. Springer Nature journal content cannot be used for inter-library loans and librarians may not upload Springer Nature journal content on a large scale into their, or any other, institutional repository. These terms of use are reviewed regularly and may be amended at any time. Springer Nature is not obligated to publish any information or content on this website and may remove it or features or functionality at our sole discretion, at any time with or without notice. Springer Nature may revoke this licence to you at any time and remove access to any copies of the Springer Nature journal content which have been saved. To the fullest extent permitted by law, Springer Nature makes no warranties, representations or guarantees to Users, either express or implied with respect to the Springer nature journal content and all parties disclaim and waive any implied warranties or warranties imposed by law, including merchantability or fitness for any particular purpose. Please note that these rights do not automatically extend to content, data or other material published by Springer Nature that may be licensed from third parties. If you would like to use or distribute our Springer Nature journal content to a wider audience or on a regular basis or in any other manner not expressly permitted by these Terms, please contact Springer Nature at onlineservice@springernature.com