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Apolipoprotein E gene polymorphisms and risk for coronary artery disease in Chinese Xinjiang Uygur and Han population
Sheng-Li Yang1, Bing-Xian He, Hui-Liang Liu
1Department of Cardiology, General Hospital of Chinese People's Armed Police Forces, Beijing 100039. yangshengli@medmail.com.cn
Insights
The apolipoprotein E (Apo E) epsilon2 allele shows a protective effect against coronary artery disease (CAD), particularly in the Uygur population. Lower epsilon2 and higher epsilon3 or epsilon4 allele frequencies are observed in CAD patients.
Area of Science:
- Genetics
- Cardiovascular Medicine
- Population Health
Background:
- Apolipoprotein E (Apo E) gene polymorphism is implicated in cardiovascular health.
- Understanding ethnic variations in Apo E allele frequencies is crucial for assessing coronary artery disease (CAD) risk.
Purpose of the Study:
- To investigate the association between apolipoprotein E (Apo E) gene polymorphism and the risk of coronary artery disease (CAD).
- To analyze the relationship between Apo E polymorphism and established cardiovascular risk factors.
Main Methods:
- Prospective evaluation of 124 patients with verified CAD or myocardial infarction and 70 controls from Han and Uygur populations.
- Genotyping of Apo E alleles (epsilon2, epsilon3, epsilon4) using PCR and HhaI digestion.
- Assessment of classical risk factors including hypertension, diabetes, tobacco use, and lipid profiles (TC, HDL, TG, LDL).
Main Results:
- Significant differences in Apo E allele frequencies were observed between Uygur and Han populations.
- CAD patients exhibited lower frequencies of the epsilon2 allele and higher frequencies of epsilon3 or epsilon4 alleles compared to controls, especially in the Uygur group.
- Apolipoprotein E (Apo E) phenotypes E2/2, E3/2, and E4/2 showed a trend towards decreased serum lipid levels (LDL, TC, TG).
Conclusions:
- Apolipoprotein E (Apo E) phenotype distribution varies significantly between Uygur and Han populations.
- The epsilon2 allele of the apolipoprotein E (Apo E) gene demonstrates a protective effect against coronary artery disease (CAD).
- Elevated frequencies of epsilon3 and epsilon4 alleles in CAD patients suggest their association with increased disease risk.
Objective:
To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors.
Methods:
A total of 124 patients (including 84 Han population and 40 Uygur population) with angiographically verified CAD or myocardial infarction were prospectively evaluated. Data referring to hypertension, diabetes, and tobacco consumption were recorded. The levels of total cholesterol (TC), high density lipoprotein (HDL) cholesterol, Apo A1 and B, and triglycerides (TG) were determined. DNA was obtained from 124 patients and 70 controls. In order to determine Apo E genotypes, DNA was PCR amplified and digested with HhaI. The genetic polymorphism of Apo E is due to three common alleles, epsilon (epsilon) 2, epsilon3, epsilon4, at a single autosomal gene locus. These alleles determine the six phenotypes E2/2, E3/3, E4/4, E4/2, E4/3, and E3/2.
Results:
In Uygur population, the frequency of the epsilon2, epsilon3, and epsilon4 was 0.155, 0.648, and 0.197 respectively. In Han population, the frequency of the epsilon2, epsilon3, and epsilon4 was 0.081, 0.772, and 0.146 respectively. In the patient group, the frequency of the epsilon2, epsilon3, and epsilon4 was 0.060, 0.758, and 0.182 respectively. In the control group, the frequency of the epsilon2, epsilon3, and epsilon4 was 0.193, 0.671, and 0.136 respectively. epsilon2 frequency of Uygur' patients and controls was 0.050 and 0.290 respectively. Serum low density lipoprotein (LDL) cholesterol, TC, and TG values tended to decrease from the Apo E-4 phenotypes to Apo E-2 phenotypes. When deletion polymorphism of epsilon2 was compared with the common risk factors for CAD, its risk ratio (RR) is 4.38.
Conclusions:
These studies confirm and find that Apo E phenotype distribution in Uygur population differs significantly from that in Han population in Xinjiang. CAD patients have significantly lower epsilon2 allele and slightly higher epsilon3 or epsilon4 allele frequency than controls, especially in Uygur population. It shows protective effects of epsilon2 on CAD.
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