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

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

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

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Nakanishi, Hideo Saito, Masaaki Yamada, Ryo Tsujikawa, Akitaka Matsuda, Fumihiko Nakata, Isao Miyake, Masahiro Oishi, Akio Yoshimura, Nagahisa Iida, Tomohiro Yamashiro, Kenji Akagi-Kurashige, Yumiko Kawaguchi, Takahisa Gotoh, Norimoto
Description	Country affiliation: Japan Author Affiliation: Nakata I ( Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.)
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.
ISSN	01460404
e-ISSN	15525783
Journal	Investigative Opthalmology & Visual Science
Issue Number	9
Volume Number	54
Language	English
Publisher	Association for Research in Vision and Ophthalmology
Publisher Date	2013-09-09
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Cholesterol Ester Transfer Proteins Genetics Choroidal Neovascularization Polymorphism, Single Nucleotide Alleles Metabolism Pathology Fluorescein Angiography Fundus Oculi Genetic Predisposition To Disease Genotype Tomography, Optical Coherence Comparative Study Research Support, Non-u.s. Gov't Discipline Ophthalmology
Content Type	Text
Resource Type	Article
Subject	Ophthalmology Sensory Systems Cellular and Molecular Neuroscience

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