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~ 363 ~
The Pharma Innovation Journal 2018; 7(4): 363-365
ISSN (E): 2277- 7695
ISSN (P): 2349-8242
NAAS Rating: 5.03
TPI 2018; 7(4): 363-365
© 2018 TPI
www.thepharmajournal.com
Received: 24-02-2018
Accepted: 25-03-2018
Neelesh Kumar Maurya
Research Scholar, Institute of
Home Science, Bundelkhand
University, Jhansi,
Uttar Pradesh, India
Prof. NS Sengar
Professor, Department of
Medicine, MLB Medical College,
Jhansi, Uttar Pradesh, India
Dr. Pratibha Arya
Assistant Professor, Institute of
Home Science, Bundelkhand
University, Jhansi,
Uttar Pradesh, India
Correspondence
Neelesh Kumar Maurya
Research Scholar, Institute of
Home Science, Bundelkhand
University, Jhansi,
Uttar Pradesh, India
Impact of Hemodialysis on lipid profile among chronic
renal failure patients (Regular and Non–Regular
Haemodialysis)
Neelesh Kumar Maurya, Prof. NS Sengar and Dr. Pratibha Arya
Abstract
Chronic Renal Failure (CRF) patients are at risk of cardiovascular diseases due to the elevation of various
forms of lipids. Many a time CRF patients live on hemodialysis on regular basis. Chronic renal failure
(CRF) is complicated by characteristic dyslipidemias. We sought to evaluate the pattern of lipid profile in
CRF patients with and without hemodialysis. Study were divided into 2 groups, Group-I: CRF patients
who never undergone hemodialysis (24) and Group-II: CRF patients on hemodialysis (24). We obtained
serum samples from patients in the morning after an overnight fast and were analyzed for total
cholesterol (TC), triglycerides (TGs), HDL, LDL and VLDL. Significant change (p<0.05) was found in
Total cholesterol (TC), HDL-C, VLDL-C, HDL-C(level) between first and second group.
Keywords: Chronic renal failure, cardiovascular disease, Haemodialysis, CKD stage – 5
1. Introduction
Chronic renal failure (CRF) is a syndrome of constant renal impairment involving loss of both
glomerular and tubular function [1]
. Progressive CRF not only leads to end stage renal disease
(ESRD), but it is associated with high cardiovascular morbidity & mortality. In fact, patients
with CRF are much more likely to die of cardiovascular complications such as dyslipidemias
than to progress to ESRD [2]
. Dyslipidemias is a very common complication of Chronic Renal
Failure (CRF). Disturbances in lipoprotein metabolism are evident even at the early stages of
CRF and usually follow a downhill course that parallels the deterioration in renal function.
Recently published studies indicate that dyslipidemias in these patients may actively
participate in the pathogenesis of Cardiovascular disease (CVD) as well as in the deterioration
of renal function [3]
. The characteristic lipid abnormalities seen in CRF patients are elevated
triglycerides, normal/reduced total cholesterol (TC), decreased High Density Lipoprotein
(HDL), normal Low Density Lipoprotein (LDL) [4]
.
With the implication of plasma lipids in the pathogenesis of atherosclerosis and ischemic heart
disease, it becomes worthwhile to study the behavior of various lipid fractions in CRF patients
[5]
. CVD constitutes the major cause of death in patients with ESRD and it is still higher in
hemodialysis patients than in post transplantation patients [6]
. ESRD Patients on hemodialysis
have abnormalities in lipoprotein structure and metabolism and have a high incidence of
cardiovascular diseases [7]
. CRF patients with CKD stage-5, their glomelurar filitration rate
have 15ml/min or less they need to kidney transplant or dialysis to survive.
The high coronary heart disease (CHD) prevalence in CRF patients is likely related to their
high frequency of dyslipidemia. The characterization of the type of lipid and lipoprotein
abnormalities should therefore be considered important in the management of CRF patients to
prevent CHD. It has also been suggested that dyslipidemia may contribute to accelerate
development of renal insufficiency. The characteristic lipid abnormalities seen in CRF patients
are elevated triglycerides, normal/reduced total cholesterol, decreased High Density
Lipoprotein (HDL), normal Low Density Lipoprotein (LDL). This disturbed lipid pattern
accelerates the process of atherosclerosis and impairs the blood supply, further damaging the
kidneys. While this process in heart and brain causes morbidity due to cardiovascular and
cerebrovascular accidents [8]
.
Lp(a) is a cholesterol-rich lipoprotein with structural similarities to LDL but contains apo(a), a
glycoprotein with sequence homology to plasminogen. Lp(a) plays a causal role in the
development of atherosclerosis and is a potentially modifiable cardiovascular disease risk
factor in hemodialysed CRF patients [9]
.
~ 364 ~
The Pharma Innovation Journal
Cardiovascular disease constitutes the major cause of death in
patients with ESRD and it is still higher in dialysis patients
than in post transplantation patients due to abnormalities in
lipids and lipoproteins structure and metabolism [10]
.
Controversies exist regarding Lp(a) levels in CRF patients
with and without hemodialysis. There are few studies that
showed Lp(a) levels were elevated in CRF patients [10, 11, 12]
.
Lp(a) levels were elevated in hemodialysed patients, Lp(a)
levels were decreased after hemodialysis [12, 14]
and Lp(a) lev-
els did not vary before and after hemodialysis [9, 15]
. With the
implication of plasma lipids and lipoproteins in the patho-
genesis of atherosclerosis and ischemic heart disease, it
becomes worthwhile to study the behavior of various lipid
fractions in CRF patients [5]
. Thus the present study was
undertaken to compare the levels of lipid profile in CRF
patients with and without hemodialysis
2. Materials and methods
This prospective, observational study was started at MLB,
Medical college Jhansi department of internal medicine and
dialysis unit. The patients were divided into two groups, both
were suffering from chronic renal failure with CKD-5 stage in
last 6-month. Twenty four patients were taken in each group.
The group first with 24 patients undergoes with haemodialysis
at regular interval, at least two times in a week. In Group
second, all patients were having same condition as like group
first but due to some reason they were unable to take
haemodialysis at least once in a week.
5 ml of venous blood samples were collected in plain tubes
after an overnight fast. After collection, the samples were
allowed to clot for half an hour following which the samples
were centrifuged and serum was analysed. Serum total
cholesterol (TC), triglycerides (TGs), HDL cholesterol (HDL-
C), LDL cholesterol (LDL-C), were measured
colorimetrically using commercially available kits on fully
auto analyzer of Clinical Biochemistry Laboratory. VLDL
cholesterol concentration was calculated using Friedewald’s
Formula [17]
.
3. Statistical analysis
Statistical data was recorded on Microsoft Excel programme.
The comparison between two groups was done by unpaired t-
test in Graph Pad Prism 7 software.
4. Results and Discussion
CRF is a worldwide health problem and is the leading cause
of morbidity and mortality in the developed world. Patients
with CRF are at high risk for CVD and cerebrovascular
disease (CBVD), and they are more likely to die of CVD than
to develop ESRD. CRF is associated with premature
atherosclerosis and increased incidence of cardiovascular
morbidity and mortality. Several factors contribute to
atherogenesis and cardiovascular disease in patients with
CRF, the notably among all is dyslipidemias [18]
. Chronic
renal failure, per se, primarily affects the metabolism of high-
density lipoprotein (HDL) and triglyceride (TG)-rich
lipoproteins [19]
In the present study we found hypertriglyceridemia in CRF
patients with and without hemodialysis. This elevated
triglyceride level is because of decreased activity of
lipoprotein lipase (LPL) which hydrolyses triglycerides and
also enhanced triglyceride synthesis in liver from free fatty
acids released from fatty tissue and muscles [20]
. Table I
revealed the biochemical parameters among CRF patients
with and without hemodialysis.
Once haemodialysis commences, continuous haemodialysis
patients develop atherogenic serum lipid profile. Total
cholesterol (TC), HDL-C, Triglycerides, VLDL-C level was
found elevated in regular haemodialysis patients as compared
to irregular Haemodialysis patients. A number of factor are
important in producing more atherogenic lipoprotein profile
in continuous haemodialysis. There was significant change
(p<0.05) found in Total cholesterol (TC), HDL-C, LDC-C,
VLDL-C, HDL-C(level) between first and second group as
shown in the table 1.
Table I: The Biochemical parameters among CRF patients with and without hemodialysis (In Mean± Standard deviation)
Parameters
Serum lipids (mg/dl)
Group -1
regular hemodialysis
patients (N=24)
(Mean ± SD)
Group -2
irregular dialysis patients
(Mean ±SD)
Unpaired t- test
P valve
Significant
difference (p<0.05)
Total cholesterol (TC) 216.5 ± 9.589 193 ± 6.223 0.0472 YES
Triglycerides (TG ) 207.4 ± 11.88 165.8 ± 11.6 0.0172 YES
High density lipoprotein (HDL) 46.29 ± 1.192 52.28 ± 1.189 0.0011 Yes
Low density lipoprotein (LDL) 111.9 ± 3.069 77.26 ± 3.187 <0.0001 Yes
Very low density lipoprotein (VLDL 69.15 ± 3.747 34.29 ± 2.347 <0.0001 Yes
5. Conclusion
It is concluded that the number of dialysis increase the level
of, Total cholesterol(TC) and Low density lipoprotein( LDL-
C),Triglycerides(TG),Very low density lipoprotein( VLDL-C)
level in regular CRF patients. HDL-C level decreases as
compare to irregular haemodialysis patients. Dialysis patients
need to cure of dyslipidemia. In irregular and regular patients,
hypertriglyceridemia treatment is necessary that will improve
the quality of life of CRF patients.
6. Acknowledgement
We acknowledge the support and cooperation from the
patients enrolled in the study. We also thankful to the staff of
Department of Medicine and Dialysis unit of MLB Medical
College, Jhansi for their valuable help and support.
7. References
1. William JM, Stephen KB, editors. Clinical Biochemistry:
metabolic and clinical aspects. 2nd ed. Philadelphia:
Churchill Livingstone, Elsevier. 2008, 145-154.
2. Godela B, Mony F. CME topic on Chronic Kidney
Disease: Whom to Screen and How to Treat, Part 1:
Definition, Epidemiology and Laboratory Testing.
Southern Medical Journal. 2010; 103(2):140-6.
3. G Brosnahan, Fraer M. Chronic Kidney Disease: Whom
to Screen and How to Treat, Part 1: Definition,
Epidemiology, and Laboratory Testing. Southern Medical
Journal. February 2010, 103-2.
~ 365 ~
The Pharma Innovation Journal
4. Amin K. Pattern of Dyslipidemia in patients with CRF.
Professional Medical Journal. 2006; 13(1):79-84.
5. Ravichandran RR, Hyperlipidemia in patients with
chronic renal failure. Journal of Post Graduate Medicine.
1983; 29(4): 212-217.
6. Fauci AS. Editor. Harrison’s principles of Internal
Medicine. USA: The McGraw Hill’s, 17th edition,
chapter 275.
7. Cressman MD. Lipoprotein(a) is an independent risk
factor for cardiovascular disease in hemodialysis patients.
Circulation, 1992, 86(2).
8. Amin K, Javed M, Abid M. Pattern of dyslipidemia in
patients with CRF. Professional Medical Journal. 2006;
13(1):79-84.
9. Cressman MD, Heyka RJ, Paganini EP. Lipoprotein(a) is
an independent risk factor for cardiovascular disease in
hemodialysis patients. Circulation. 1992; 86(2):475-82.
10. Fauci AS, Kasper DL, Longo DL, Braunwald E, Hauser
SL, Larry Jameson J et al editors. Harrison’s principles of
Internal Medicine. 17th ed. New York: McGraw Hill,
Health Professions Division, 2008, 1772–6.
11. Kronenberg F, Lingenhel A, Neyer U. Prevalence of
Dyslipidemic risk factors in hemodialysis and CAPD
patients. Kidney International. 2003; 63(Suppl 84):113-
16.
12. Kalra OP, Khaira A, Gambhir JK. Lipoprotein(a) in
Chronic Renal Failure: Effect of Maintenance
Hemodialysis. Hemodialysis International. 2003;
7(4):326–33.
13. Yerkey MW, Kernis SJ, Franklin BA. Renal Dysfunction
and Acceleration of Coronary Disease. Heart. 2004;
90:961–6.
14. Kandoussi A, Cachera C, Pagniez D. Plasma level of
lipoprotein Lp(a) is high in predialysis or hemodialysis,
but not in CAPD. Kidney International. 1992; 42:424-5.
15. Barbagallo CM, Averna MR, Sparachio V. Lp (a) levels
in end-stage renal failure and renal transplantation.
Nephron. 1993; 64:560-4.
16. Ravichandran RR, Nerurkar SV, Acharya VN.
Hyperlipidemia in patients with chronic renal failure.
Journal of Post Graduate Medicine. 1983; 29(4):212-17.
17. Friedewald WT, Levy RI, Fredrickson DS. Estimation of
the Concentration of Low-Density Lipoprotein
Cholesterol in Plasma, Without Use of the Preparative
Ultracentrifuge. Clinical Chemistry, 1972, 18(6).
18. Agarwal SK, Srivastava RK. Chronic Kidney Disease in
India: Challenges and Solutions. Nephron Clinical
Practice. 2009; 111:c197-c203.
19. Vaziri ND, Moradi H. Mechanisms of Dyslipidemia of
chronic renal failure. Hemodialysis International. 2006;
10:1-7.
20. Janicki K, Molas G, Furmaga J. Abnormal lipoprotein
metabolism in hemodialysis patients, Annales
Universitatis Mariae Curie – Sklodowska Lublin Polonia.
2007; 62:311-14.

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Impact of Hemodialysis on lipid profile among chronic renal failure patients (Regular and Non–Regular Haemodialysis)

  • 1. ~ 363 ~ The Pharma Innovation Journal 2018; 7(4): 363-365 ISSN (E): 2277- 7695 ISSN (P): 2349-8242 NAAS Rating: 5.03 TPI 2018; 7(4): 363-365 © 2018 TPI www.thepharmajournal.com Received: 24-02-2018 Accepted: 25-03-2018 Neelesh Kumar Maurya Research Scholar, Institute of Home Science, Bundelkhand University, Jhansi, Uttar Pradesh, India Prof. NS Sengar Professor, Department of Medicine, MLB Medical College, Jhansi, Uttar Pradesh, India Dr. Pratibha Arya Assistant Professor, Institute of Home Science, Bundelkhand University, Jhansi, Uttar Pradesh, India Correspondence Neelesh Kumar Maurya Research Scholar, Institute of Home Science, Bundelkhand University, Jhansi, Uttar Pradesh, India Impact of Hemodialysis on lipid profile among chronic renal failure patients (Regular and Non–Regular Haemodialysis) Neelesh Kumar Maurya, Prof. NS Sengar and Dr. Pratibha Arya Abstract Chronic Renal Failure (CRF) patients are at risk of cardiovascular diseases due to the elevation of various forms of lipids. Many a time CRF patients live on hemodialysis on regular basis. Chronic renal failure (CRF) is complicated by characteristic dyslipidemias. We sought to evaluate the pattern of lipid profile in CRF patients with and without hemodialysis. Study were divided into 2 groups, Group-I: CRF patients who never undergone hemodialysis (24) and Group-II: CRF patients on hemodialysis (24). We obtained serum samples from patients in the morning after an overnight fast and were analyzed for total cholesterol (TC), triglycerides (TGs), HDL, LDL and VLDL. Significant change (p<0.05) was found in Total cholesterol (TC), HDL-C, VLDL-C, HDL-C(level) between first and second group. Keywords: Chronic renal failure, cardiovascular disease, Haemodialysis, CKD stage – 5 1. Introduction Chronic renal failure (CRF) is a syndrome of constant renal impairment involving loss of both glomerular and tubular function [1] . Progressive CRF not only leads to end stage renal disease (ESRD), but it is associated with high cardiovascular morbidity & mortality. In fact, patients with CRF are much more likely to die of cardiovascular complications such as dyslipidemias than to progress to ESRD [2] . Dyslipidemias is a very common complication of Chronic Renal Failure (CRF). Disturbances in lipoprotein metabolism are evident even at the early stages of CRF and usually follow a downhill course that parallels the deterioration in renal function. Recently published studies indicate that dyslipidemias in these patients may actively participate in the pathogenesis of Cardiovascular disease (CVD) as well as in the deterioration of renal function [3] . The characteristic lipid abnormalities seen in CRF patients are elevated triglycerides, normal/reduced total cholesterol (TC), decreased High Density Lipoprotein (HDL), normal Low Density Lipoprotein (LDL) [4] . With the implication of plasma lipids in the pathogenesis of atherosclerosis and ischemic heart disease, it becomes worthwhile to study the behavior of various lipid fractions in CRF patients [5] . CVD constitutes the major cause of death in patients with ESRD and it is still higher in hemodialysis patients than in post transplantation patients [6] . ESRD Patients on hemodialysis have abnormalities in lipoprotein structure and metabolism and have a high incidence of cardiovascular diseases [7] . CRF patients with CKD stage-5, their glomelurar filitration rate have 15ml/min or less they need to kidney transplant or dialysis to survive. The high coronary heart disease (CHD) prevalence in CRF patients is likely related to their high frequency of dyslipidemia. The characterization of the type of lipid and lipoprotein abnormalities should therefore be considered important in the management of CRF patients to prevent CHD. It has also been suggested that dyslipidemia may contribute to accelerate development of renal insufficiency. The characteristic lipid abnormalities seen in CRF patients are elevated triglycerides, normal/reduced total cholesterol, decreased High Density Lipoprotein (HDL), normal Low Density Lipoprotein (LDL). This disturbed lipid pattern accelerates the process of atherosclerosis and impairs the blood supply, further damaging the kidneys. While this process in heart and brain causes morbidity due to cardiovascular and cerebrovascular accidents [8] . Lp(a) is a cholesterol-rich lipoprotein with structural similarities to LDL but contains apo(a), a glycoprotein with sequence homology to plasminogen. Lp(a) plays a causal role in the development of atherosclerosis and is a potentially modifiable cardiovascular disease risk factor in hemodialysed CRF patients [9] .
  • 2. ~ 364 ~ The Pharma Innovation Journal Cardiovascular disease constitutes the major cause of death in patients with ESRD and it is still higher in dialysis patients than in post transplantation patients due to abnormalities in lipids and lipoproteins structure and metabolism [10] . Controversies exist regarding Lp(a) levels in CRF patients with and without hemodialysis. There are few studies that showed Lp(a) levels were elevated in CRF patients [10, 11, 12] . Lp(a) levels were elevated in hemodialysed patients, Lp(a) levels were decreased after hemodialysis [12, 14] and Lp(a) lev- els did not vary before and after hemodialysis [9, 15] . With the implication of plasma lipids and lipoproteins in the patho- genesis of atherosclerosis and ischemic heart disease, it becomes worthwhile to study the behavior of various lipid fractions in CRF patients [5] . Thus the present study was undertaken to compare the levels of lipid profile in CRF patients with and without hemodialysis 2. Materials and methods This prospective, observational study was started at MLB, Medical college Jhansi department of internal medicine and dialysis unit. The patients were divided into two groups, both were suffering from chronic renal failure with CKD-5 stage in last 6-month. Twenty four patients were taken in each group. The group first with 24 patients undergoes with haemodialysis at regular interval, at least two times in a week. In Group second, all patients were having same condition as like group first but due to some reason they were unable to take haemodialysis at least once in a week. 5 ml of venous blood samples were collected in plain tubes after an overnight fast. After collection, the samples were allowed to clot for half an hour following which the samples were centrifuged and serum was analysed. Serum total cholesterol (TC), triglycerides (TGs), HDL cholesterol (HDL- C), LDL cholesterol (LDL-C), were measured colorimetrically using commercially available kits on fully auto analyzer of Clinical Biochemistry Laboratory. VLDL cholesterol concentration was calculated using Friedewald’s Formula [17] . 3. Statistical analysis Statistical data was recorded on Microsoft Excel programme. The comparison between two groups was done by unpaired t- test in Graph Pad Prism 7 software. 4. Results and Discussion CRF is a worldwide health problem and is the leading cause of morbidity and mortality in the developed world. Patients with CRF are at high risk for CVD and cerebrovascular disease (CBVD), and they are more likely to die of CVD than to develop ESRD. CRF is associated with premature atherosclerosis and increased incidence of cardiovascular morbidity and mortality. Several factors contribute to atherogenesis and cardiovascular disease in patients with CRF, the notably among all is dyslipidemias [18] . Chronic renal failure, per se, primarily affects the metabolism of high- density lipoprotein (HDL) and triglyceride (TG)-rich lipoproteins [19] In the present study we found hypertriglyceridemia in CRF patients with and without hemodialysis. This elevated triglyceride level is because of decreased activity of lipoprotein lipase (LPL) which hydrolyses triglycerides and also enhanced triglyceride synthesis in liver from free fatty acids released from fatty tissue and muscles [20] . Table I revealed the biochemical parameters among CRF patients with and without hemodialysis. Once haemodialysis commences, continuous haemodialysis patients develop atherogenic serum lipid profile. Total cholesterol (TC), HDL-C, Triglycerides, VLDL-C level was found elevated in regular haemodialysis patients as compared to irregular Haemodialysis patients. A number of factor are important in producing more atherogenic lipoprotein profile in continuous haemodialysis. There was significant change (p<0.05) found in Total cholesterol (TC), HDL-C, LDC-C, VLDL-C, HDL-C(level) between first and second group as shown in the table 1. Table I: The Biochemical parameters among CRF patients with and without hemodialysis (In Mean± Standard deviation) Parameters Serum lipids (mg/dl) Group -1 regular hemodialysis patients (N=24) (Mean ± SD) Group -2 irregular dialysis patients (Mean ±SD) Unpaired t- test P valve Significant difference (p<0.05) Total cholesterol (TC) 216.5 ± 9.589 193 ± 6.223 0.0472 YES Triglycerides (TG ) 207.4 ± 11.88 165.8 ± 11.6 0.0172 YES High density lipoprotein (HDL) 46.29 ± 1.192 52.28 ± 1.189 0.0011 Yes Low density lipoprotein (LDL) 111.9 ± 3.069 77.26 ± 3.187 <0.0001 Yes Very low density lipoprotein (VLDL 69.15 ± 3.747 34.29 ± 2.347 <0.0001 Yes 5. Conclusion It is concluded that the number of dialysis increase the level of, Total cholesterol(TC) and Low density lipoprotein( LDL- C),Triglycerides(TG),Very low density lipoprotein( VLDL-C) level in regular CRF patients. HDL-C level decreases as compare to irregular haemodialysis patients. Dialysis patients need to cure of dyslipidemia. In irregular and regular patients, hypertriglyceridemia treatment is necessary that will improve the quality of life of CRF patients. 6. Acknowledgement We acknowledge the support and cooperation from the patients enrolled in the study. We also thankful to the staff of Department of Medicine and Dialysis unit of MLB Medical College, Jhansi for their valuable help and support. 7. References 1. William JM, Stephen KB, editors. Clinical Biochemistry: metabolic and clinical aspects. 2nd ed. Philadelphia: Churchill Livingstone, Elsevier. 2008, 145-154. 2. Godela B, Mony F. CME topic on Chronic Kidney Disease: Whom to Screen and How to Treat, Part 1: Definition, Epidemiology and Laboratory Testing. Southern Medical Journal. 2010; 103(2):140-6. 3. G Brosnahan, Fraer M. Chronic Kidney Disease: Whom to Screen and How to Treat, Part 1: Definition, Epidemiology, and Laboratory Testing. Southern Medical Journal. February 2010, 103-2.
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