Apolipoprotein E gene polymorphism and risk for coronary heart disease in the Chinese population: a meta-analysis of 61 studies including 6634 cases and 6393 controls

PLoS One. 2014 Apr 22;9(4):e95463. doi: 10.1371/journal.pone.0095463. eCollection 2014.

Abstract

Background: Numerous studies have evaluated the association between the apolipoprotein E (apoE) gene polymorphisms in coronary heart disease (CHD). However, the results remain uncertain. We carried out a meta-analysis to derive a more comprehensive estimation of the association in Chinese population.

Methods: Case-control studies in Chinese and English publications were identified by searching databases of PubMed, EMBASE, Web of Science, CNKI, CBM, Wanfang, VIP and hand searching of relevant journals and the reference lists of retrieved articles. Odds ratio (OR) and 95% confidence interval (CI) were applied to assess the strength of the associations. Subgroup analysis and sensitivity analysis were performed to explore the between-study heterogeneity.

Results: We finally identified 61 relevant studies which comprised 6634 case-patients and 6393 controls. The pooled OR for ε4 carriers was 96% higher than the ε3/3 genotype for CHD (OR, 1.96; 95% CI, 1.70 to 2.24; P<0.001). However, there was no evidence of statistically significant association between ε2 carriers and risk of CHD (OR, 1.02; 95% CI, 0.91 to 1.13; P = 0.729). In the subgroup analysis, different endpoints may partially account for the heterogeneity. No publication bias was found.

Conclusions: Our meta-analysis suggests that the apoE ε4 allele may be a risk factor for CHD in the Chinese population, however, ε2 allele has no significant association.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein E3 / genetics
  • Apolipoprotein E4 / genetics
  • Apolipoproteins E / genetics*
  • Asian People / genetics*
  • Case-Control Studies
  • China
  • Coronary Artery Disease / genetics
  • Coronary Disease / genetics*
  • Genetic Predisposition to Disease*
  • Humans
  • Odds Ratio
  • Polymorphism, Genetic*
  • Publication Bias
  • Risk Factors

Substances

  • Apolipoprotein E3
  • Apolipoprotein E4
  • Apolipoproteins E

Grants and funding

This study is supported by “Twelve Five” National Key Technology R&D Program of China (Grant No. 2011BAI11B05)(http://www.most.gov.cn/eng/programmes1/200610/t20061009_36224.htm) and Beijing Natural Science Foundation of China(Grant No. 7132078) (http://www.bjkw.gov.cn/n244495/index.html). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.