Association of the ephreceptor tyrosinekinase-type A2 (EPHA2) gene polymorphism rs3754334 with age-related cataract risk: a meta-analysis

PLoS One. 2013 Aug 16;8(8):e71003. doi: 10.1371/journal.pone.0071003. eCollection 2013.

Abstract

Background: Recent clinical studies have assessed the association of various polymorphisms on the ephreceptor tyrosinekinase-type A2 (EPHA2) with the risk for age-related cataract in populations of different ethnic/racial backgrounds, but inconsistent results have been obtained.

Objective: This meta-analysis aimed to identify if any polymorphism(s) might be commonly present in different ethnic/racial populations in association with the age-related cataract risk.

Methods: The PubMed and Web of Science databases (up to December 1, 2012) were searched for clinical studies on the association of EPHA2 polymorphisms with the risk for age-related cataract. The polymorphisms that were assessed in all eligible studies were analyzed for their association with the risk for age-related cataract using different models.

Results: Three studies were identified, which were conducted, respectively, on white Americans in the Unites States and on Asians in Indian and China. The polymorphism, rs3754334, was the only one studied in all these three studies and was therefore the focus of this meta-analysis. No publication bias or heterogeneity was found. Our analysis results demonstrated that rs3754334 was associated with the risk of any cataracts in the recessive (OR = 1.202, 95% CI: 1.051-1.375, P = 0.007) and Codominant (OR = 1.194, 95% CI: 1.035-1.378, P = 0.015) models, but its association with cortical or nuclear phenotype of age-related cataract was not evident.

Conclusion: Polymorphism, rs3754334, might be a variant on the EPHA2 gene that is commonly associated with the risk for age-related cataract in different ethnical and geographical populations.

Publication types

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

MeSH terms

  • Age Factors
  • Cataract / ethnology
  • Cataract / genetics*
  • Databases, Bibliographic
  • Genetic Association Studies
  • Genetic Predisposition to Disease*
  • Humans
  • Models, Genetic
  • Phenotype
  • Polymorphism, Single Nucleotide*
  • Racial Groups
  • Receptor, EphA2 / genetics*
  • Risk Factors

Substances

  • Receptor, EphA2

Grants and funding

This work was supported by the National Natural Science Foundation of China (NSFC), grants (#81270989 and #81200669), and the Research Fund for the Doctoral Program of Higher Education of China (#20120071120089). None of the authors has any financial conflict of interest to disclose. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.