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Published on: November 18, 2013
Association between Apolipoprotein C-III Gene Polymorphisms and Coronary Heart Disease: A Meta-analysis
Jing-Zhan Zhang1, Xiang Xie1, Yi-Tong Ma1
1Department of Cardiology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830054, China.
Insights
Genetic variations in apolipoprotein C-III (APOC3) gene, specifically SstI and T-455C polymorphisms, are linked to increased risk of coronary heart disease (CHD). However, the C-482T polymorphism shows no significant association with CHD susceptibility.
Area of Science:
- Genetics
- Cardiovascular Disease Epidemiology
Background:
- Polymorphisms in the apolipoprotein C-III (APOC3) gene are implicated in coronary heart disease (CHD) risk.
- Previous studies on APOC3 gene polymorphisms and CHD have yielded conflicting results.
Purpose of the Study:
- To conduct a comprehensive meta-analysis investigating the association between three main APOC3 gene polymorphisms (SstI, T-455C, C-482T) and CHD.
- To provide a more precise estimation of the relationship between these genetic variations and CHD susceptibility.
Main Methods:
- Systematic literature search of multiple databases (PubMed, Web of Science, Wanfang, SinoMed, CNKI).
- Inclusion of 31 published studies examining APOC3 polymorphisms and CHD.
- Statistical analysis using odds ratios (ORs) with 95% confidence intervals (CIs) under various genetic models, employing Review Manager and Stata software.
Main Results:
- The APOC3 SstI polymorphism was significantly associated with increased CHD susceptibility (OR=1.14, P=0.003 for allelic contrast).
- The APOC3 T-455C polymorphism also showed a significant association with increased CHD risk (OR=1.19, P<0.0001 for allelic contrast).
- No significant association was found between the APOC3 C-482T polymorphism and CHD susceptibility across all genetic models.
Conclusions:
- The APOC3 SstI and T-455C polymorphisms are confirmed to significantly increase susceptibility to coronary heart disease.
- The APOC3 C-482T polymorphism does not appear to be associated with CHD risk based on current evidence.
Abstract:
Polymorphisms in the apolipoprotein C-III (APOC3) gene have been reported to be associated with coronary heart disease (CHD), but the data so far have been conflicting. To derive a more precise estimation of these associations, we performed a meta-analysis to investigate the three main polymorphisms (SstI, T-455C, C-482T) of APOC3 in all published studies. Databases including PubMed, Web of Science, Wanfang, SinoMed and CNKI were systematically searched. The association was assessed using odds ratios (ORs) with 95% confidence intervals (CIs). The statistical analysis was performed using Review Manager 5.3.3 and Stata 12.0. A total of 31 studies have been identified. The pooled odds ratio (OR) for the association between the APOC3 gene polymorphisms and CHD and its corresponding 95% confidence interval (95% CI) were evaluated by random or fixed effect models. A statistical association between APOC3 SstI polymorphism and CHD susceptibility was observed under an allelic contrast model (P= 0.003, OR = 1.14, 95% CI = 1.05-1.24), dominant genetic model (P= 0.01, OR = 1.14, 95% CI = 1.03-1.26), and recessive genetic model (P= 0.02, OR = 1.35, 95% CI = 1.06-1.71), respectively. A significant association between the APOC3 T-455C polymorphism and CHD was also detected under an allelic contrast (P < 0.0001, OR = 1.19, 95% CI = 1.10-1.29), dominant genetic model (P= 0.0003, OR = 1.24, 95% CI = 1.11-1.39) and recessive genetic model (P= 0.04, OR = 1.30, 95% CI = 1.01-1.67). No significant association between the APOC3 C-482T polymorphism and CHD was found under an allelic model (P= 0.94, OR = 1.00, 95% CI = 0.93-1.08), dominant genetic model (P= 0.20, OR = 1.07, 95% CI = 0.97-1.18) or recessive genetic model (P= 0.13, OR = 0.90, 95% CI = 0.79-1.03). This meta-analysis revealed that the APOC3 SstI and T-455C polymorphisms significantly increase CHD susceptibility. No significant association was observed between the APOC3 C-482T polymorphism and CHD susceptibility.
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