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[Association between apolipoprotein A5 gene polymorphism and coronary heart disease in the Han population from
Shan Yuan1, Yi-tong Ma, Xiang Xie
1Key Laboratory of Cardiovascular Disease Research of Xinjiang, Urumqi 830054, China.
Insights
The c.553G>T polymorphism in the apolipoprotein A5 (ApoA5) gene is linked to coronary heart disease (CHD) risk in Xinjiang
Area of Science:
- Genetics
- Cardiovascular Disease
- Biochemistry
Background:
- Coronary heart disease (CHD) is a leading cause of mortality globally.
- Genetic factors play a significant role in CHD susceptibility.
- The apolipoprotein A5 (ApoA5) gene is implicated in lipid metabolism and cardiovascular risk.
Purpose of the Study:
- To investigate the association between the ApoA5 gene c.553G>T polymorphism and CHD in the Han population of Xinjiang.
- To examine the influence of serum lipid levels on this association.
Main Methods:
- Genotyping of the ApoA5 c.553G>T polymorphism using polymerase chain reaction and restriction fragment length polymorphism analysis in 486 CHD patients and 501 controls.
- Measurement of serum lipid profiles (triglyceride, total cholesterol) in all participants.
Main Results:
- A significant difference in genotype distribution was observed between CHD patients and controls (P=0.013).
- Carrying the T allele (TT + GT genotypes) was associated with an increased risk of CHD (OR=1.753, P<0.05), independent of other risk factors.
- Individuals with the T allele exhibited higher serum triglyceride levels and, in the CHD group, higher total cholesterol levels compared to those with the GG genotype.
Conclusions:
- The ApoA5 c.553G>T polymorphism influences serum triglyceride and total cholesterol levels in the Xinjiang Han population.
- This polymorphism is associated with CHD development, with the T allele potentially acting as an independent risk factor.
Objective:
The aim is to investigate the association between coronary heart disease (CHD) and c.553G>T polymorphism of apolipoprotein A5 (ApoA5) gene and the influence of serum lipid level in the Han ethnic population of Xinjiang.
Methods:
The polymorphism of ApoA5 gene in 486 patients with CHD and 501 controls was analyzed by methods of polymerase chain reaction and restriction fragment length polymorphism analysis. Level of serum lipid in each patient was detected at the same time.
Results:
There was significant difference in the distribution of genotypes between CHD group and controls group (χ(2)=8.757, P=0.013). Non-conditioned logistic regression analyses, after adjusted for age, gender, smoking, total serum cholesterol, presence of hypertension and diabetes, revealed that individuals who carried T allele (TT + GT genotype) had an increased risk of CHD, compared to GG genotype (OR=1.753, 95%CI: 1.030-2.983, P<0.05). There was also a remarkable difference noticed in the level of serum triglyceride by genotypes in CHD group and control group (t=-5.242, P<0.01; t=-3.499, P=0.001). Individuals in the two groups who carried T allele had higher level of serum triglyceride than those carried GG genotype. Individuals in CHD group who carried T allele had higher level of serum total cholesterol than those carried GG genotype (t=-2.465, P=0.014).
Conclusion:
It seemed that the c.553G>T polymorphism of ApoA5 gene had influenced on the level of serum triglyceride and the total cholesterol among Han population in Xinjiang. c.553G>T polymorphism was associated with the development of CHD, while T allele might be an influencing risk factor on CHD.
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