Original
Article#
Prevalence of
Dyslipidemia in Young Adult Indian Population
AM Sawant,
Dhanashri Shetty, R Mankeshwar, Tester F Ashavaid*
Abstract
Background:
Cardiovascular diseases (CVD) are the major cause of morbidity and mortality in
our society with dyslipidemia contributing significantly to atherosclerosis.
Thus measurement of plasma lipids would help in identifying people at risk for
CVD. The goal of this study was to ascertain the prevalence of Dyslipidemia
among young adult population in urban India.
Material and Methods : The study was conducted for a period of one year –
from 1st January 2006 to 31st December 2006. Around 1805 subjects with ³ 40 age group
were selected from a population of approximately 9000 urban dwellers who had
attended annual general health check ups in P. D. Hinduja National Hospital and
Medical research Center. Health status was evaluated by physical check ups,
complete fasting lipid profiles and blood glucose levels. Dyslipidemia risk and
impaired blood sugar levels were determined as per National Cholesterol
Education Program (NCEP) – Adult Treatment Panel (ATP) III guidelines and
American Diabetes Association (ADA) respectively.
Results: The
prevalence of dyslipidemia was observed to be higher in males then in females.
Among participants who had a total Cholesterol (TC) concentration ³ 200mg/dl,
38.7% were males and 23.3% were females. High density lipoprotein cholesterol
(HDL-C) was abnormally low in 64.2% males and 33.8% in females. The increase of
prevalence of hypercholesterolemia and hypertriglyceridemia was more prominent
in 31-40 age group than in £ 30 age group.
Conclusion: The
low percentage of adults with controlled lipid concentrations suggests that
there is a need for awareness programs for the prevention and control of
Dyslipidemia and impaired blood sugar levels. ©
INTRODUCTION
Cardiovascular diseases (CVD) are the most prevalent
cause of death and disability in both developed as well as developing
countries.1 South Asians
around the globe have the highest rates of Coronary Artery Disease (CAD).2 According to National Commission on Macroeconomics and Health (NCMH), a
government of India undertaking, there would be around 62 million patients with
CAD by 2015 in India and of these, 23 million would be patients younger than 40
years of age.3 CAD is usually due to atherosclerosis of large and
medium sized arteries and Dyslipidemia has been found to be one of the most
important contributing factor.4 As it has long been known that lipid
abnormalities are major risk factors for premature CAD,6,2 studies
on the prevalence of these risk factors are urgently needed. In this
retrospective study, we report the prevalence of dyslipidemia in young adult
Indian population.
Material and Methods
Design and Data
Collection
The study
population consisted of 8967 members who attended Health check-up program from
January - December 2006 at P. D. Hinduja National Hospital and Medical Research
Center, Mumbai, India. Of these, around 1805 healthy individuals were selected
from the Medical database which included, demographics
(age, gender), anthropometric measurements (relative body weight, height),
lifestyle related factors (smoking status, alcohol consumption, diet and
physical activity) and clinical findings (hypertension, diabetes, ischemic
heart disease, medication profile and family history). Blood samples were
collected by venipuncture after an overnight fast for 12-14 hours. Venous blood
was collected in plain and fluoride bulbs for measurement of serum lipids and
glucose respectively.
Serum Lipid and
Glucose Analysis
The analysis
was carried on an automated clinical chemistry analyzer; Beckman Synchron Lx20.
Serum glucose was measured by oxygen rate method employing a Beckman oxygen
electrode (glucose oxidase). TC, low density lipoprotein cholesterol (LDL-C),
HDL-C and triglyceride (TG) concentrations were measured by International
Federation of Clinical Chemistry (IFCC) approved enzymatic methods. Beckman
reagents and calibrators were used for the analysis. HDL-N and LDL-N are
directly estimated by ready to use stable liquid reagents. Control sera were
included in each batch of samples analyzed. As a part of external quality
assurance, our laboratory is enrolled with the proficiency testing surveys of
the College of American (CAP) Pathologists and is the first hospital lab in
India to be CAP accredited.
Defenitions and
Preferred Cutoff Values
For serum
lipids, we referred to NCEP - ATP III Guidelines.4,5 According to these standard guidelines, hypercholesterolemia is defined as TC
>200mg/dl, LDL-C as >100mg/dl, hypertriglyceridemia as TG >150mg/dl
and HDL-C <40mg/dl. Dyslipidemia is defined by presence of one or more than
one abnormal serum lipid concentration. For serum Glucose levels, we referred
to ADA Guidelines.7 Persons with fasting blood glucose >126mg/dl
or who were on medication for diabetes was considered as having diabetes
mellitus.
Statistical
Analysis
The
statistical analysis was performed using the SPSS (version 13.0). Lipid and
glucose levels were expressed as the mean ± SD. The data was further
categorized according to age group and gender. The normality of the data was
checked by the Shapiro-Wilk procedure. As the underlying data distribution is
non-normal, Mann Whitney U test was applied to test the relationship of
independent and dependent variables. Pearson’s chi square test was applied in
comparisons of independent and dependent proportions. Odds ratio (OR) and 95%
confidence interval (CI) was calculated to find out the significance of the
data. A p value <0.05 was considered deemed significant. Prevalence of
dyslipidemia by means of its determinants was calculated using the prevalence
rate formula: number of patients per total number of all subjects at the time
of study multiplied by 100. Results were expressed as percentages.
RESULTS
The study
population was comprised of 1805 subjects that included 1128 males and 677
females (Fig. 1) and the clinical features of the subjects are shown in (Table
1). On applying NCEP and ADA guidelines we found out that nearly 80% of the
subjects had atleast one abnormal parameter.
Increased
levels of fasting and postprandial blood glucose, hypercholesterolemia,
hypertriglyceridemia and increased levels of LDL-C were found to be more in
males. Similarly decreased HDL-C levels were again found to be more in males
(Table 2).
On further
comparing between males and females according to age we found significantly
increased levels of fasting blood glucose, postprandial blood glucose,
hypercholesterolemia, hypertriglyceridemia, low HDL, and high LDL to be in
31-40 year old males and females than in £ 30 year old males and females.
There were no significant differences in low HDL concentration between age
groups in males and females (Figs. 2 and 3).
The Figure 4
shows specific prevalence of dyslipidemia and impaired blood glucose levels
according to gender. The prevalence of elevated fasting and postprandial blood
glucose, hypercholesterolemia, hypertriglyceridemia, low HDL, and high LDL were
significantly higher in males than in females (34.1% vs. 22.1%, 13.2% vs. 8.1%,
38.6% vs. 23.3%, 42.6% vs. 17.2%, 64.2% vs 33.8%, 74.3% vs. 61.2%)
respectively.
DISSCUSSION
This study
is a step towards evaluating the lipids and lipoprotiens and glucose levels in
health urban Indian population. The study reveals the prevalence of hypercholesterolemia,
hypertriglyceridemia and abnormally high LDL-C and low HDL-C levels which are
well-known risk factors for cardiovascular diseases in all age groups. Our
results are consistent with the previous cross-sectional study conducted among
selected industrial population wherein increased prevalence of dyslipidemia in
young adults was found to be one of the major contributors of CVD.6 Increased prevalence of high fasting glucose and serum lipids were more
prominent in 31 – 40 age group as compared to £ 30 years which means
the risk of dyslipidemia increases as the age advances. In our study we
observed, both fasting and postprandial impaired glucose levels to be more in
31-40 age group males and of these 7% were found to be actually diabetic i.e.
they were either on some medication or were newly diagnosed. This means the
remaining subjects with impaired blood glucose levels are on their way to
develop diabetes, which is an important risk factor for CAD. Enas et al.
in Coronary artery disease in Indians (CADI) study reports the prevalence of
diabetes to be three to six times higher among south Asian’s than Europeans,
Americans and other Asians.2
The high
prevalence of hypercholesterolemia, hypertriglyceridemia and low HDL, in our
31-40 years age group is a major cause of concern. It has been observed that in
comparison with western population, a relatively lower level of cholesterol
appears to predispose Indians to CAD.7 Also in a Chennai based
hospital study, it was shown that around 75% of patients with myocardial
infarction (MI) had TC levels <200mg/dl indicating that the threshold for
the TC levels above which it posses a risk for CAD is low in Indians.8 The crude prevalence of hypertriglyceridemia differs between the age groups and
it was higher in men than in women. The contributing factor for
hypertriglyceridemia in our population could be our diet rich in carbohydrates.9 High TG levels have been associated with increased levels of small dense LDL
which are considered to be highly atherogenic.10 Increased
prevalence of low HDL has been reported earlier by Enas etal. who found that only 4% of Asian Indian men and 5% Asian
Indian women had optimal HDL levels.11
Low HDL-C
levels are stronger predictor of occurrence and reoccurrence of MI and stroke
and are also associated with premature and severe CAD.12 Oxidative
modification of LDL-C is a key process of atherosclerosis and elevated LDL-C
has been recognized as primary risk factor for CAD by NCEP – ATPIII.13 In our study increased LDL-C has been found to be contributing majorly to
dyslipidemia irrespective of age and gender. On comparing the prevalence of
dyslipidemia and impaired blood glucose (IBG) levels between males and females,
we observed it to be higher in males suggesting this group at higher risk of
dyslipidemia, which in turn can lead to increased risk of developing CAD.
Comparing our
data with a Turkish study conducted on similar lines, lead to the observation
that in both the studies, prevalence of dyslipidemia was more in males but the
percentage prevalence in our population was higher indicating Indians being at
higher risk.14 Diet with high fat and calorie intake and lack of
physical activity would be the major culprits of dyslipidemia in our
population. References have shown that our diets are rich in saturated fats.
Besides it also involves overcooking of food which results in destruction of
nutrients like folate, deep frying and refrying in the same oil leading to
trans fatty acids formation which probably contributes to increase of
Dyslipidemia in our population.15 The influence of diet on
Dyslipidemia was best seen in the Canadian study wherein 3 groups: a control
group, a group that was administered statin and a group with dietary
modification was included. The lipid levels were checked at baseline and again
after 4 weeks. A drastic reduction in lipid levels was observed in statin and
dietary modified groups as compared to control group. However, between the two
they did not vary much.16 This means
therapeutic intervention i.e. statin and dietary interventions seems to have
the same effect, and the latter seems to be a more viable option.
CONCLUSION
This study
revealed the increased prevalence of dyslipidemia to be more prevalent in 31-40
year males, suggesting that this group is at increased risk of developing CAD
leading to young infarcts. Combination lifestyle therapies i.e., enhanced
physical activity and dietary modification and therapeutic intervention17,18 would help us in treatment and management of
dyslipidemia.
Acknowledgements
We
acknowledge the support and help provided by the Medical Record Department of
P. D. Hinduja National Hospital and Medical Research Center, Mahim, Mumbai.
REFERENCES
1. Chaturvedi V, Bhargava B.
Health Care Delivery for Coronary Heart Disease in India- Where are we Headed. Am Heart Hosp J 2007;5:32-37.
2. Enas
EA, Chacko V, Pazhoor SG, Chennikkara H and Devarapalli P. Dyslipidemia in
South Asian Patients. Current Atherosclerosis Reports 2007;9:367-74.
3. Indrayan
A. Forecasting vascular disease cases and associated mortality in India. Reports of the
National Commission on Macroeconomics and Health. Ministry
of Health and Family Welfare, India 2005. Available at:
http://www.whoindia.org/EN/Section102/Section201_888.htm. Accessed November 2,
2006.
4. Executive Summary of the
Third Report of the National Cholesterol Education Program (NCEP) Expert Panel
on Detection, Evaluation, and treatment of High Blood Cholesterol in Adults
(Adult Treatment Panel III) [special communication]. JAMA 2001;285:2486-2947.
5. Third Report of the National
Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and
Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final
report [special communication]. Circulation 2002;106:
3143-3421.
6. Reddy KS, Prabhakaran D,
Chaturvedi V, Jeemon P, Thankappan KR, Ramakrishnan L, Mohan BVM, Pandav CS,
Ahmed FU, Meera R, Joshi PP, Amin RB, Ahuja RC, Das MS, and Jaison TM. Methods for establishing a surveillance system for cardiovascular
disease in Indian industrial populations. Bulletin of the World
Health Organization 2006;84:461-69.
7. American Diabetes
Association. Diagnosis and classification of diabetes
mellitus. Diabetes Care 2006;29(suppl
1): S43-48. Available at:
http://www.diabetes.org/diabetes-prevention/pre-diabetes.jsp
8. Kumar S, Roy S. Tropical
Heart Disease in India. In: Mantosh Panja editors. Dyslipidemia
in Indians. Mumbai. Indian College of
Physicians 2005;109-18.
9. Krishnaswami V,
Radhakrishnan T, John BV, and Mathew A. Pattern of ischaemic heart disease: a
clinical study. J Indian Med Asso 1970;55:153-57.
10. Enas
EA, Senthilkumar A, Chennikkara H, and Bjurlin MA. Prudent Diet and Preventive
nutrition from Pediatrics to Geriatrics: Current Knowledge and Practical
recommendations. Indian Heart J 2003;55:310-38.
11. Mora S, Szklo M, and Otwos
JD. LDL particle subclasses, LDL particle size, and carotid
atherosclerosis in the Multiethnic Study of Atherosclerosis (MESA). Atherosclerosis 2007;192:211-17.
12. Enas
EA, Yusuf S, and Mehta JL. Prevalence of Coronary Artery Disease in Asian-
Indians. Am J Cardiol 1992;70:945-49.
13. Pearson TA, Bulkley BH,
Achuff SC, Kwiterovich PO, and Gordis L. The association of low levels of HDL
cholesterol and arteriography defined coronary artery disease. Am J
Epidermiol 1979;109:285-95.
14. Soysal A, Demiral Y, Soysal
D, Ucku R, Koseoglu M, Aksakoglu G. The prevalence of metabolic syndrome among ypung adults in Izmir,
Turkey. Anadolu Kardiyol Derg 2005;5:196-201.
15. Enas AE, Senthilkumar A,
Hancy C, and Marc AB. Prudent diet and preventive nutrition from pediatrics to
geriatrics: current knowledge and practical recommendations. Indian Heart J 2003;55:310-38.
16. David JAJ, Cyril WCK,
Augustine M, Dorothea AF, Julia MWW, Russell D, Azadeh E, Tina LP, Edward V,
Karen GL, Elke aT, Robert GJ, Lawrence AL and Philip WC. Effects
of a dietary portfolio of cholesterol – lowering foods vs lovastatin on serum
lipids and C-reactive protein. JAMA 2003;290: 17. Mc-Carron DA, Reusser ME. Reducing Cardiovascular Disease Risk with Diet. Obesity
Research 2001;9(suppl.4):335s-340s.
18. Jenkins DJA, Kendall CWC, Marchie A, Faulkner D, Wong JMW, DeSouza R, Emam A, Parker T, Vidgen E, Lapsley KG, Trautwein EA, Josse RG, Leiter LA, and Connelly PW. Effects of a Dietary portfolio of Cholesterol- Lowering foods vs Lovastain on serum lipids and C- reactive protein. JAMA 2003;290:502-10. |