Candidate gene association study for diabetic retinopathy in Chinese patients with type 2 diabetes

被引:1
|
作者
Yang, Xiufen [1 ,2 ]
Deng, Yu [1 ,3 ]
Gu, Hong [1 ]
Ren, Xuetao [1 ,4 ]
Li, Na [1 ]
Lim, Apiradee [5 ]
Snellingen, Torkel [4 ]
Liu, Xipu [4 ]
Wang, Ningli [1 ]
Liu, Ningpu [1 ]
机构
[1] Capital Med Univ, Beijing Tongren Eye Ctr, Beijing Tongren Hosp, Beijing Ophthalmol & Visual Sci Key Lab, Beijing 100730, Peoples R China
[2] Capital Med Univ, Friendship Hosp, Dept Ophthalmol, Beijing 100730, Peoples R China
[3] Capital Med Univ, Fu Xing Hosp, Dept Ophthalmol, Beijing 100730, Peoples R China
[4] Sekwa Inst Vis Sci, Beijing, Peoples R China
[5] Prince Songkla Univ, Fac Sci & Technol, Dept Math & Comp Sci, Pattani, Thailand
来源
MOLECULAR VISION | 2014年 / 20卷
基金
北京市自然科学基金;
关键词
ENDOTHELIAL GROWTH-FACTOR; ALDOSE REDUCTASE GENE; SUSCEPTIBILITY GENES; VEGF POLYMORPHISMS; RISK-FACTORS; RECEPTORS; PROGRESSION; HERITABILITY; RANIBIZUMAB; BEVACIZUMAB;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: To investigate whether variants in a set of eight candidate genes are associated with diabetic retinopathy (DR) in a cohort of Chinese patients with type 2 diabetes mellitus (T2DM). Methods: Case-control study. Patients with T2DM were recruited from the Desheng community in urban Beijing and assigned into a DR group or diabetic without retinopathy (DWR) group, based on the duration of diabetes and grading of fundus images. Twenty-six single-nucleotide polymorphisms (SNPs) within eight candidate genes, including PPAR., vascular endothelial growth factor (VEGF) and its receptor kinase insert domain receptor (KDR), erythropoietin, aldose reductase, protein kinase C-beta, angiotensin-converting enzyme, and intercellular adhesion molecule 1, were analyzed using the MassARRAY genotyping system. Results: A total of 500 patients with T2DM (216 with DR and 284 with DWR) were enrolled in the study. Significant associations of DR were noted with genotypes of four SNPs-rs699947 (p<0.001), rs833061 (p=0.001), rs13207351 (p<0.001), and rs2146323 (p=0.006)-in the VEGF gene and one variant, rs2071559, in the KDR gene (p=0.034). After adjustment for covariates, significant association of DR remained with the homozygous genotype of the minor allele for the SNPs rs699947 (odds ratio [OR] = 3.54, 95% confidence interval [CI]: 1.12-11.19), rs833061 (OR = 3.72, 95% CI: 1.17-11.85), rs13207351 (OR = 3.76, 95% CI: 1.21-11.71), and rs2146323 (OR = 2.8, 95% CI: 1.46-5.37) in the VEGF gene as well as the SNP rs2071559 (OR = 1.62, 95% CI: 1.08-2.41) in the KDR gene. However, only rs699947 and rs13207351 in the VEGF gene remained statistically significant after Bonferroni correction. No associations were found in other genes tested. Conclusions: These data expanded previous observations on the association of DR with variants in the VEGF gene in Chinese patients with T2DM. Moreover, a possible association between DR and KDR polymorphisms is suggested.
引用
收藏
页码:200 / 214
页数:15
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