Association between vascular endothelial growth factor +936 C/T gene polymorphism and age-related macular degeneration
Author(s) -
Yanming Jiang,
Liang Ge,
Liqiang Wang,
Jingjing Jiang,
Gaiping Du,
Yifei Huang
Publication year - 2013
Publication title -
journal of international medical research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 57
eISSN - 1473-2300
pISSN - 0300-0605
DOI - 10.1177/0300060513475570
Subject(s) - macular degeneration , medicine , genotype , odds ratio , vascular endothelial growth factor , choroidal neovascularization , gastroenterology , pathogenesis , angiogenesis , oncology , vegf receptors , ophthalmology , genetics , gene , biology
Objectives The pathogenesis of age-related macular degeneration (AMD) remains unknown. Vascular endothelial growth factor (VEGF) is an important regulator of angiogenesis and a target for inhibition therapy in wet AMD. This study investigated the association between the VEGF +936 C/T gene polymorphism and AMD, in a Chinese Han population.Methods Patients with AMD, and age- and sex-matched controls were enrolled. Restriction fragment length polymorphism was used to analyse the VEGF +936 polymorphism in the promoter and the 3′ untranslated region of the gene.Results The study included 200 AMD patients and 200 control subjects. There was a significantly higher prevalence of the TT genotype among AMD patients (9.0%) compared with controls (3.5%); the odds ratio for this genotype in AMD patients was 2.73 (95% confidence intervals 1.11, 6.68). There were no significant associations between any genotype and AMD subphenotypic categories (early, geographic atrophy, choroidal neovascularization).Conclusions The present study findings suggested that the VEGF +936 TT genotype was associated with AMD among Han Chinese patients.
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