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Journal Presentation
Department of
Endocrinology
1. Dr Mahbub Islam
2. Dr MD Azimuddin
3. Dr Pappon Kumar Chondo
4. Dr Mitun Debnath
5. Dr. Tanveer kamal Fahim
Phase-A, MD Pulmonology
Introduction
Metabolic Syndrome is a Poor
Predictor of Incident Diabetes
Compared with Hemoglobin A1c
(HbA1C) in a General Japanese
Population
Kaneko M, Suzuki H, Watanabe H, Oda E, Aizawa Y
(2011) Metabolic Syndrome is a Poor Predictor of Incident
Diabetes Compared with
Hemoglobin A1c (Hba1c) in a General Japanese
Population. J Diabetes Metab S:2. doi:10.4172/2155-
6156.S2-001
 Metabolic syndrome (MetS) is considered to
be a risk factor of diabetes and cardiovascular
disease (CVD). However, its predictive value
for diabetes beyond fasting plasma glucose
(FPG) is questioned.
 MetS is a pre-morbid condition rather than a
clinical diagnosis, and should thus exclude
individuals with established diabetes or known
CVD
 MetS is not a better predictor of diabetes
than prediabetes because the risk for incident
diabetes among those with prediabetes but
not MetS was almost triple that of those with
MetS but not prediabetes. Even for the
purpose of predicting CVD, it may
be dangerous for individuals to be diagnosed
with MetS
 On the other hand, the usefulness of
hemoglobin A1c (HbA1c) for predicting
diabetes has been reported in several studies
 In the present study the usefulness of
MetS has been evaluated as a
predictor of incident diabetes
comparing with other predictors of
incident diabetes including HbA1c in a
general Japanese population.
Definition of Mets
 MetS was defined as the clustering of three
or more of the following:
1) high BMI: BMI ≥ 25 kg/m2, 2) high BP:
systolic BP≥ 130 mmHg and/or diastolic BP ≥
85 mmHg and/or antihypertensive medication
3) high triglycerides: triglycerides ≥ 1.7
mmol/L, 4) low HDL cholesterol: HDL
cholesterol < 1.0 mmol/L in men and <
1.3 mmol/L in women, and 5) high FPG: FPG
≥ 5.6 mmol/L.
Aim of the study
 To evaluate the usefulness of metabolic
syndrome (MetS) as a predictor of incident
diabetes comparing with other predictors of
diabetes including hemoglobin A1c (HbA1c)
Materials and
Methods
It is a retrospective five-year follow-up study from annual
health examination data in a community including 1,997
Japanese subjects without diabetes at baseline.
Logistic regressions using incident diabetes as a
dependent variable were calculated for each predictor
adjusted for age, sex and drinking status.
Area under receiver operating characteristic curves
(AUCs) and population attributable risk fractions (PAFs)
of incident diabetes were calculated for each predictor.
Study
Subjects
This community-based, retrospective
cohort study was based on annual
health examination consisted of a
medical history, physical examination,
blood examination, chest x-ray, and
electrocardiography.This report includes
2,153 subjects who took the health
examination including FPG and HbA1c
in 1998 as a baseline study and
subsequently received the examination
in 2003.
Measurements
 After an overnight fast, blood samples
were obtained to measure FPG, HbA1c,
triglycerides, high-density lipoprotein
(HDL) cholesterol,alanine
aminotransferase (ALT), and gamma
glutamyltransferase.(GGT). Blood
pressure was measured in supine
position after a five minutes rest. Body
mass index (BMI) was calculated as
weight in kilograms divided by the
square of height in meters. Values of
HbA1c are presented as NGSP %.
Results
 The odds ratios (95% confidence interval)
of incident diabetes for MetS, fasting
plasma glucose (FPG) ≥5.6 mmol/L and
HbA1c ≥ 6.0% were 5.39 (2.72-10.7), 9.52
(5.08-17.9), and 33.5 (13.0-86.4),
respectively. The AUCs (95% confidence
interval) of diagnosing incident diabetes for
FPG, HbA1c, and MetS were 0.82 (0.76-
0.88), 0.89(0.82-0.95) and 0.63 (0.53-0.72)
respectively.
Result (contd..)
 The optimal cutoff points of FPG,
HbA1c, and body mass index were 5.3
mmol/L, 6.0% and 23.5 kg/m2
respectively. The sensitivity and
specificity of FPG, HbA1c
and MetS for predicting diabetes were
0.67 and 0.80, 0.88 and 0.83, and
0.33 and 0.93, respectively. The PAFs
of FPG ≥ 5.3 mmol/L, HbA1c ≥ 6.0%,
and MetS were 59%, 86%, and 27%,
respectively
Statistical
analysis
 Logistic regressions were performed
using incident diabetes as
a dependent variable adjusted for sex,
age and drinking status. Areas under
receiver operating characteristic
curves (AUCs) for diagnosing incident
diabetes were calculated. Population
attributable risk fractions (PAFs) were
calculated for each predictor. P values
of less than 0.05 were considered as
significant.
Table 1: Baseline data stratified by incident diabetes.
diabetes non-diabetes p
n 43 1,954
male sex (%) 37.2 22.9 0.03
age (years) 65.3 ± 7.6 61.6 ± 8.9 0.006
fasting plasma glucose
(mmol/L)
5.56 ± 0.56 4.92 ± 0.48 <0.0001
hemoglobin A1c (%) 6.3 ± 0.5 5.6 ± 0.4 <0.0001
body mass index
(kg/m2)
23.9 ± 2.7 22.6 ± 2.7 0.002
systolic blood pressure
(mmHg)
133.3 ± 14.0 128.9 ± 15.5 0.07
diastolic blood pressure
(mmHg)
79.8 ± 11.7 78.0 ± 10.0 0.3
HDL cholesterol
(mmol/L)
1.47 ± 0.30 1.67 ± 0.40 .002
triglycerides (mmol/L) 1.49 ± 0.74 1.14 ± 0.73 0.002
alanine
aminotransferase (U/L)
26.3 ± 21.9 19.1 ± 12.8 0.0004
gamma
glutamyltransferase
(U/L)
21.7 ± 15.6 16.7 ± 18.8 0.08
total cholesterol
(mmol/L)
5.74 ± 0.79 5.62 ± 0.87 0.4
smoker (%) 14.0 11.0 0.5
everyday drinker
(%)
20.9 18.5 0.7
Table 2: Prevalence of metabolic syndrome* and its
components by incident
diabetes.
diabetes non-diabetes p
metabolic
syndrome
32.6 7.0 <0.0001
high fasting
plasma glucose
51.2 9.3 <0.0001
high body mass
index
39.5 18.5 0.0005
high blood
pressure
62.8 53.3 0.2
high triglycerides 32.6 12.7 0.0001
low HDL
cholesterol
18.6 7.8 0.01
Odds ratios of incident diabetes
for numerical variables.
odds ratio* (95%
confidence interval)
p
metabolic syndrome 5.39 (2.72-10.7) <0.0001
fasting plasma glucose ≥
5.6 mmol/L
9.52 (5.08-17.9) <0.0001
body mass index ≥ 25
kg/m2
2.98 (1.59-5.58) 0.0006
high blood pressure † 1.17 (0.61-2.24) 0.6
triglycerides ≥ 1.7 mmol/L 3.07 (1.59-5.92) 0.0008
low HDL cholesterol 1.88 (0.76-4.67) .2
hemoglobin A1c ≥ 6.0% 33.5 (13.0-86.4) <0.0001
alanine aminotransferase
≥ 22 U/L
2.05 (1.10-3.83) 0.02
Table 4: Odds ratios of incident diabetes for
categorical variables.
odds ratio* (95%
confidence interval)
p
metabolic syndrome 5.39 (2.72-10.7) <0.0001
fasting plasma glucose ≥
5.6 mmol/L
9.52 (5.08-17.9) <0.0001
body mass index ≥ 25
kg/m2
2.98 (1.59-5.58) 0.0006
high blood pressure † 1.17 (0.61-2.24) 0.6
triglycerides ≥ 1.7 mmol/L 3.07 (1.59-5.92) 0.0008
low HDL cholesterol# 1.88 (0.76-4.67) 0.2
hemoglobin A1c ≥ 6.0% 33.5 (13.0-86.4) <0.0001
alanine aminotransferase
≥ 22 U/L
2.05 (1.10-3.83) 0.02
Table 5: Area under receiver operating characteristic
curves (AUCs) for predicting
incident diabetes.
AUC (95% confidence
interval)
p
fasting plasma
glucose
0.82 (0.76-0.88) <0.0001
hemoglobin A1c 0.89 (0.82-0.95) <0.0001
metabolic syndrome 0.63 (0.53-0.72) 0.004
body mass index 0.66 (0.57-0.74) 0.0005
alanine
aminotransferase
0.60 (0.50-0.69) 0.03
Table 6: Optimal cutoff points (sensitivity; specificity) and PAFs * for
incident diabetes.
[*population attributable risk fractions, #PAF was 25% for body mass
index ≥ 25
Kg/m2]
Cutoff point sensitivity; specificity PAF*
fasting plasma
glucose
5.3 mmol/L 0.67; 0.80 59%
hemoglobin A1c 6.0% 0.88; 0.83 86%
metabolic
syndrome
0.33; 0.93 27%
body mass index 23.5 kg/m2 0.63; 0.66 43%
alanine
aminotransferase
22 U/L 0.42; 0.75 22%
Discussion
 In the present five-year follow-up study
among a general Japanese
population.MetS was a poor predictor of
incident diabetes compared with FPG or
HbA1c (AUC; 0.63 vs. 0.82 or 0.89) and
was comparable to BMI or ALT (AUC;
0.63 vs. 0.66 or 0.60).
 The relative risks of incident diabetes
were 3.53-5.17 in various definitions of
MetS [7].AUCs of MetS for predicting
incident diabetes were ranging from 0.68
to 0.85; sensitivity ranged from 0.224 to
0.722, and specificity ranged from 0.613
Discussion (contd)
 In our present study, HbA1c was the best
predictor of incident diabetes. HbA1c has
been suggested to be superior to FPG for
the prediction of vascular disease and
death from any cause among nondiabetic
subjects
 Thus, the usefulness of MetS diagnosis is
low for either predicting diabetes compared
with FPG or HbA1c or predicting CVD
compared with hypertension or smoking
in Japanese where obesity is not prevailing.
Limitation
1. results are hypothetical because the
subjects in the present study were not
randomly recruited from the community but
recruited because their information about
diabetic history and other relevant data
were retrospectively available, and the
number of subjects was relatively small.
2. We used BMI instead of waist
circumference as an obesity marker
because waist circumference was not
available.
 Some original data were lost and have
now only incomplete data in 1998 and
2003 where 14,244 subjects were
included. However,information about
medical history remained in only 1997
subjects and biased regarding sex and
age.
 Accordingly, the present study
was based on logistic regression using
data at only two time points.
Thus,drop-out subjects were ignored.
Conclusion
 MetS is a poor predictor of diabetes
compared with FPG or HbA1c and
A1C was the best predictor of
diabetes in a general Japanese
population.
Metabolic syndrome vs HbA1c

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Metabolic syndrome vs HbA1c

  • 1.
  • 2. Journal Presentation Department of Endocrinology 1. Dr Mahbub Islam 2. Dr MD Azimuddin 3. Dr Pappon Kumar Chondo 4. Dr Mitun Debnath 5. Dr. Tanveer kamal Fahim Phase-A, MD Pulmonology
  • 4. Metabolic Syndrome is a Poor Predictor of Incident Diabetes Compared with Hemoglobin A1c (HbA1C) in a General Japanese Population Kaneko M, Suzuki H, Watanabe H, Oda E, Aizawa Y (2011) Metabolic Syndrome is a Poor Predictor of Incident Diabetes Compared with Hemoglobin A1c (Hba1c) in a General Japanese Population. J Diabetes Metab S:2. doi:10.4172/2155- 6156.S2-001
  • 5.  Metabolic syndrome (MetS) is considered to be a risk factor of diabetes and cardiovascular disease (CVD). However, its predictive value for diabetes beyond fasting plasma glucose (FPG) is questioned.  MetS is a pre-morbid condition rather than a clinical diagnosis, and should thus exclude individuals with established diabetes or known CVD
  • 6.  MetS is not a better predictor of diabetes than prediabetes because the risk for incident diabetes among those with prediabetes but not MetS was almost triple that of those with MetS but not prediabetes. Even for the purpose of predicting CVD, it may be dangerous for individuals to be diagnosed with MetS  On the other hand, the usefulness of hemoglobin A1c (HbA1c) for predicting diabetes has been reported in several studies
  • 7.  In the present study the usefulness of MetS has been evaluated as a predictor of incident diabetes comparing with other predictors of incident diabetes including HbA1c in a general Japanese population.
  • 8. Definition of Mets  MetS was defined as the clustering of three or more of the following: 1) high BMI: BMI ≥ 25 kg/m2, 2) high BP: systolic BP≥ 130 mmHg and/or diastolic BP ≥ 85 mmHg and/or antihypertensive medication 3) high triglycerides: triglycerides ≥ 1.7 mmol/L, 4) low HDL cholesterol: HDL cholesterol < 1.0 mmol/L in men and < 1.3 mmol/L in women, and 5) high FPG: FPG ≥ 5.6 mmol/L.
  • 9. Aim of the study
  • 10.  To evaluate the usefulness of metabolic syndrome (MetS) as a predictor of incident diabetes comparing with other predictors of diabetes including hemoglobin A1c (HbA1c)
  • 12. It is a retrospective five-year follow-up study from annual health examination data in a community including 1,997 Japanese subjects without diabetes at baseline. Logistic regressions using incident diabetes as a dependent variable were calculated for each predictor adjusted for age, sex and drinking status. Area under receiver operating characteristic curves (AUCs) and population attributable risk fractions (PAFs) of incident diabetes were calculated for each predictor.
  • 14. This community-based, retrospective cohort study was based on annual health examination consisted of a medical history, physical examination, blood examination, chest x-ray, and electrocardiography.This report includes 2,153 subjects who took the health examination including FPG and HbA1c in 1998 as a baseline study and subsequently received the examination in 2003.
  • 16.  After an overnight fast, blood samples were obtained to measure FPG, HbA1c, triglycerides, high-density lipoprotein (HDL) cholesterol,alanine aminotransferase (ALT), and gamma glutamyltransferase.(GGT). Blood pressure was measured in supine position after a five minutes rest. Body mass index (BMI) was calculated as weight in kilograms divided by the square of height in meters. Values of HbA1c are presented as NGSP %.
  • 18.  The odds ratios (95% confidence interval) of incident diabetes for MetS, fasting plasma glucose (FPG) ≥5.6 mmol/L and HbA1c ≥ 6.0% were 5.39 (2.72-10.7), 9.52 (5.08-17.9), and 33.5 (13.0-86.4), respectively. The AUCs (95% confidence interval) of diagnosing incident diabetes for FPG, HbA1c, and MetS were 0.82 (0.76- 0.88), 0.89(0.82-0.95) and 0.63 (0.53-0.72) respectively.
  • 19. Result (contd..)  The optimal cutoff points of FPG, HbA1c, and body mass index were 5.3 mmol/L, 6.0% and 23.5 kg/m2 respectively. The sensitivity and specificity of FPG, HbA1c and MetS for predicting diabetes were 0.67 and 0.80, 0.88 and 0.83, and 0.33 and 0.93, respectively. The PAFs of FPG ≥ 5.3 mmol/L, HbA1c ≥ 6.0%, and MetS were 59%, 86%, and 27%, respectively
  • 21.  Logistic regressions were performed using incident diabetes as a dependent variable adjusted for sex, age and drinking status. Areas under receiver operating characteristic curves (AUCs) for diagnosing incident diabetes were calculated. Population attributable risk fractions (PAFs) were calculated for each predictor. P values of less than 0.05 were considered as significant.
  • 22. Table 1: Baseline data stratified by incident diabetes. diabetes non-diabetes p n 43 1,954 male sex (%) 37.2 22.9 0.03 age (years) 65.3 ± 7.6 61.6 ± 8.9 0.006 fasting plasma glucose (mmol/L) 5.56 ± 0.56 4.92 ± 0.48 <0.0001 hemoglobin A1c (%) 6.3 ± 0.5 5.6 ± 0.4 <0.0001 body mass index (kg/m2) 23.9 ± 2.7 22.6 ± 2.7 0.002 systolic blood pressure (mmHg) 133.3 ± 14.0 128.9 ± 15.5 0.07 diastolic blood pressure (mmHg) 79.8 ± 11.7 78.0 ± 10.0 0.3 HDL cholesterol (mmol/L) 1.47 ± 0.30 1.67 ± 0.40 .002 triglycerides (mmol/L) 1.49 ± 0.74 1.14 ± 0.73 0.002 alanine aminotransferase (U/L) 26.3 ± 21.9 19.1 ± 12.8 0.0004 gamma glutamyltransferase (U/L) 21.7 ± 15.6 16.7 ± 18.8 0.08 total cholesterol (mmol/L) 5.74 ± 0.79 5.62 ± 0.87 0.4 smoker (%) 14.0 11.0 0.5 everyday drinker (%) 20.9 18.5 0.7
  • 23. Table 2: Prevalence of metabolic syndrome* and its components by incident diabetes. diabetes non-diabetes p metabolic syndrome 32.6 7.0 <0.0001 high fasting plasma glucose 51.2 9.3 <0.0001 high body mass index 39.5 18.5 0.0005 high blood pressure 62.8 53.3 0.2 high triglycerides 32.6 12.7 0.0001 low HDL cholesterol 18.6 7.8 0.01
  • 24. Odds ratios of incident diabetes for numerical variables. odds ratio* (95% confidence interval) p metabolic syndrome 5.39 (2.72-10.7) <0.0001 fasting plasma glucose ≥ 5.6 mmol/L 9.52 (5.08-17.9) <0.0001 body mass index ≥ 25 kg/m2 2.98 (1.59-5.58) 0.0006 high blood pressure † 1.17 (0.61-2.24) 0.6 triglycerides ≥ 1.7 mmol/L 3.07 (1.59-5.92) 0.0008 low HDL cholesterol 1.88 (0.76-4.67) .2 hemoglobin A1c ≥ 6.0% 33.5 (13.0-86.4) <0.0001 alanine aminotransferase ≥ 22 U/L 2.05 (1.10-3.83) 0.02
  • 25. Table 4: Odds ratios of incident diabetes for categorical variables. odds ratio* (95% confidence interval) p metabolic syndrome 5.39 (2.72-10.7) <0.0001 fasting plasma glucose ≥ 5.6 mmol/L 9.52 (5.08-17.9) <0.0001 body mass index ≥ 25 kg/m2 2.98 (1.59-5.58) 0.0006 high blood pressure † 1.17 (0.61-2.24) 0.6 triglycerides ≥ 1.7 mmol/L 3.07 (1.59-5.92) 0.0008 low HDL cholesterol# 1.88 (0.76-4.67) 0.2 hemoglobin A1c ≥ 6.0% 33.5 (13.0-86.4) <0.0001 alanine aminotransferase ≥ 22 U/L 2.05 (1.10-3.83) 0.02
  • 26. Table 5: Area under receiver operating characteristic curves (AUCs) for predicting incident diabetes. AUC (95% confidence interval) p fasting plasma glucose 0.82 (0.76-0.88) <0.0001 hemoglobin A1c 0.89 (0.82-0.95) <0.0001 metabolic syndrome 0.63 (0.53-0.72) 0.004 body mass index 0.66 (0.57-0.74) 0.0005 alanine aminotransferase 0.60 (0.50-0.69) 0.03
  • 27. Table 6: Optimal cutoff points (sensitivity; specificity) and PAFs * for incident diabetes. [*population attributable risk fractions, #PAF was 25% for body mass index ≥ 25 Kg/m2] Cutoff point sensitivity; specificity PAF* fasting plasma glucose 5.3 mmol/L 0.67; 0.80 59% hemoglobin A1c 6.0% 0.88; 0.83 86% metabolic syndrome 0.33; 0.93 27% body mass index 23.5 kg/m2 0.63; 0.66 43% alanine aminotransferase 22 U/L 0.42; 0.75 22%
  • 29.  In the present five-year follow-up study among a general Japanese population.MetS was a poor predictor of incident diabetes compared with FPG or HbA1c (AUC; 0.63 vs. 0.82 or 0.89) and was comparable to BMI or ALT (AUC; 0.63 vs. 0.66 or 0.60).  The relative risks of incident diabetes were 3.53-5.17 in various definitions of MetS [7].AUCs of MetS for predicting incident diabetes were ranging from 0.68 to 0.85; sensitivity ranged from 0.224 to 0.722, and specificity ranged from 0.613
  • 30. Discussion (contd)  In our present study, HbA1c was the best predictor of incident diabetes. HbA1c has been suggested to be superior to FPG for the prediction of vascular disease and death from any cause among nondiabetic subjects  Thus, the usefulness of MetS diagnosis is low for either predicting diabetes compared with FPG or HbA1c or predicting CVD compared with hypertension or smoking in Japanese where obesity is not prevailing.
  • 32. 1. results are hypothetical because the subjects in the present study were not randomly recruited from the community but recruited because their information about diabetic history and other relevant data were retrospectively available, and the number of subjects was relatively small. 2. We used BMI instead of waist circumference as an obesity marker because waist circumference was not available.
  • 33.  Some original data were lost and have now only incomplete data in 1998 and 2003 where 14,244 subjects were included. However,information about medical history remained in only 1997 subjects and biased regarding sex and age.  Accordingly, the present study was based on logistic regression using data at only two time points. Thus,drop-out subjects were ignored.
  • 35.  MetS is a poor predictor of diabetes compared with FPG or HbA1c and A1C was the best predictor of diabetes in a general Japanese population.