Association between the cholesteryl ester transfer protein gene and polypoidal choroidal vasculopathy

Invest Ophthalmol Vis Sci. 2013 Sep 9;54(9):6068-73. doi: 10.1167/iovs.13-11605.

Abstract

Purpose: To determine whether genetic variants in the lipid-associated genes are related to the risk of developing polypoidal choroidal vasculopathy (PCV) in a Japanese population.

Methods: Five hundred eighty-one patients with PCV and 793 controls were enrolled in the study. Association analysis of allele and genotype frequencies was performed for the following single-nucleotide polymorphisms (SNPs) that are associated with high-density lipoprotein cholesterol levels in blood: rs493258 at the hepatic lipase gene (LIPC), rs3764261 at the cholesteryl ester transfer protein gene (CETP), and rs12678919 at the lipoprotein lipase gene (LPL). A further model adjusting for age-related maculopathy susceptibility 2 (ARMS2) A69S, complement factor H (CFH) I62V, age, sex, and smoking status was used to confirm the independent association of these SNPs with other covariates.

Results: CETP rs3764261 was significantly associated with the development of PCV; the frequency of the minor allele A was higher in the PCV cases (24.0%) than in the control subjects (18.5%) (P = 0.0025; odds ratio [OR], 1.41; 95% confidence interval, 1.13-1.75). Furthermore, we found an independent association of CETP variants with age, sex, smoking status, and genetic background of ARMS2 A69S, CFH I62V, LIPC rs493258, and LPL rs12678919 (P = 0.0013; OR, 1.50). LIPC rs493258 and LPL rs12678919 did not show significant associations with the development of PCV (P > 0.05).

Conclusion: CETP variants are associated a risk of developing PCV among the Japanese population.

Keywords: CETP; PCV; case-control study; lipid.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alleles
  • Cholesterol Ester Transfer Proteins / genetics*
  • Cholesterol Ester Transfer Proteins / metabolism
  • Choroidal Neovascularization / genetics*
  • Choroidal Neovascularization / metabolism
  • Choroidal Neovascularization / pathology
  • DNA / genetics*
  • Female
  • Fluorescein Angiography
  • Fundus Oculi
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Tomography, Optical Coherence

Substances

  • CETP protein, human
  • Cholesterol Ester Transfer Proteins
  • DNA