Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis

PLoS One. 2013;8(3):e60472. doi: 10.1371/journal.pone.0060472. Epub 2013 Mar 27.

Abstract

Background: The association between polymorphism 4b/a, T-786C and G894T in endothelial NO synthase gene (eNOS) and ischemic stroke (IS) remains controversial in Asian. A meta-analysis was performed to better clarify the association between eNOS gene and IS risk.

Methods: Based on the search of PubMed, Web of Science (ISI), CNKI (National Knowledge Infrastructure), Wan Fang Med Online and CBM (Chinese Biology Medical Literature Database) databases, all eligible case-control or cohort studies were identified. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) from fixed and random effect models were calculated. Heterogeneity among studies was evaluated using the I(2). Meta-regression was used to explore the potential sources of between-study heterogeneity. Begg's test was used to estimate publication bias.

Results: Our study included 27 articles, contained 28 independent case-control studies, involved a total of 3,742 cases and 3,691 controls about 4b/a, 1,800 cases and 1,751 controls about T-786C and 2,747 cases and 2,872 controls about G894T. A significant association of 4a allele with increased risk of IS was found in dominant (FEM: OR = 1.498, 95% CI = 1.329-1.689), recessive (FEM: OR = 2.132, 95% CI = 1.383-3.286) and codominant (REM: OR = 1.456, 95% CI = 1.235-1.716) models. For T-786C and G894T, there were significant associations with dominant and codominant genetic models, but not with recessive genetic model.

Conclusions: The meta-analysis indicated that eNOS gene 4b/a, T-786C, G894T polymorphism might be associated with IS.

Publication types

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

MeSH terms

  • Asian People / genetics*
  • Brain Ischemia / complications
  • Brain Ischemia / genetics*
  • Case-Control Studies
  • Genetic Heterogeneity
  • Genetic Predisposition to Disease*
  • Humans
  • Nitric Oxide Synthase Type III / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Publication Bias
  • Risk Factors
  • Stroke / complications
  • Stroke / genetics*

Substances

  • NOS3 protein, human
  • Nitric Oxide Synthase Type III

Grants and funding

This study was supported by the Natural Science Foundation of Shandong Province (grant # ZR2010HM100). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.