Four complement factor H gene polymorphisms in association with AMD: A meta-analysis

Arch Gerontol Geriatr. 2016 May-Jun:64:123-9. doi: 10.1016/j.archger.2016.01.011. Epub 2016 Jan 28.

Abstract

Aim: To investigate the possible association between CFH gene polymorphisms -543G>A (rs1410996), A473A (rs2274700), -257C>T (rs3753394), IVS15 (rs1329428) and AMD risk.

Methods: We searched the published literature in the Medline and Scopus from inception to May 2015. A meta-analysis was performed by the programs RevMan 5.1 and Stata 12.0, and the Pooled odds ratio (OR) with 95% confidence interval (CI) was calculated in fixed or random effect model based on heterogeneity test among studies.

Results: Nineteen studies with a total of 10,676 subjects were included in the present meta-analysis. A statistical significant association was observed between AMD risk and CFH -543G>A polymorphism with OR of 1.77 (95% CI, 1.47-2.12), 2.24 (95% CI, 1.71-2.94), 0.49 (95% CI, 0.38-0.62) and 0.25 (95% CI, 0.18-0.37) in additive, dominant, recessive and codominant models, respectively. Similar results were obtained in polymorphisms A473A, -257C>T, IVS15. Furthermore, stratified analysis for ethnicity showed a significantly strong association between -543G>A, A473A polymorphisms and AMD risk.

Conclusion: The present meta-analysis suggested that CFH -543G>A, A473A, -257C>T, and IVS15 polymorphisms might be moderately associated with AMD risk. This conclusion warrants confirmation by further studies.

Keywords: Complement factor H; Macular degeneration; Meta-analysis; Polymorphism.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Aged
  • Asian People / genetics*
  • Complement Factor H / genetics*
  • Humans
  • Macular Degeneration / genetics*
  • Polymorphism, Single Nucleotide

Substances

  • Complement Factor H