Rabbind Singh Amrathlal, Gupta Rahul, Shukla Manish, Jain Anupreeti, Shukla Dhananjay
Centre for Genomics, Molecular and Human Genetics, Jiwaji University, Gwalior, India.
Department of Exercise Physiology, Lakshmibai National Institute of Physical Education, Gwalior, India.
Ophthalmic Genet. 2022 Feb;43(1):80-87. doi: 10.1080/13816810.2021.1992786. Epub 2021 Oct 25.
Diabetes mellitus type 2 is often described as the global pandemic of the 21 century with India emerging as its capital. Microvascular complications such as retinopathy associated with diabetes are a serious world health problem, leading to the already existing burden of blindness. The aim of this study was to determine whether VEGF gene polymorphisms rs35569394 and rs699947 are associated with DR in North Indians.
North Indian subjects, diabetic controls with no retinopathy (DR I, n = 51), subjects with diabetes with mild-moderate retinal changes (DR II, n = 50), and subjects with diabetes with severe retinopathy with/without retinal neovascularization (DR III, n = 55) were recruited for this study. Genotyping of the VEGF gene I/D polymorphism was done by PCR and C/A polymorphism by PCR-RFLP method.
DD-genotype was 2.73 times over expressed among DR III category ( = .02; OR: 2.73; 95% CI: 1.20-6.19) as compared to DR I category among male subgroup. C-allele (rs699947) had 1.66-times more exposure among DR III as compared to DR I (C vs. A allele; = .063; OR: 1.66; 95% CI: 0.97-2.84), probably due to high linkage disequilibrium between both the polymorphisms.
Results of our study support the hypothesis that D-allele and DD-genotype of rs35569394 have deleterious effect on the progression of DR. C-allele had skewed frequency towards DR III subjects owing to strong linkage disequilibrium between C-allele (rs699947) and D-allele (rs35569394).
2型糖尿病常被描述为21世纪的全球大流行病,印度已成为其重灾区。糖尿病相关的微血管并发症如视网膜病变是一个严重的全球健康问题,导致了现有的失明负担。本研究的目的是确定血管内皮生长因子(VEGF)基因多态性rs35569394和rs699947是否与北印度人的糖尿病视网膜病变(DR)相关。
本研究招募了北印度受试者,包括无视网膜病变的糖尿病对照组(DR I,n = 51)、有轻度至中度视网膜病变的糖尿病受试者(DR II,n = 50)以及有严重视网膜病变伴或不伴视网膜新生血管形成的糖尿病受试者(DR III,n = 55)。采用聚合酶链反应(PCR)对VEGF基因I/D多态性进行基因分型,采用PCR-限制性片段长度多态性(PCR-RFLP)方法对C/A多态性进行基因分型。
在男性亚组中,与DR I组相比,DR III组中DD基因型的表达量高出2.73倍(P = 0.02;比值比:2.73;95%置信区间:1.20 - 6.19)。与DR I组相比,DR III组中C等位基因(rs699947)的暴露量高出1.66倍(C等位基因与A等位基因相比;P = 0.063;比值比:1.66;95%置信区间:0.97 - 2.84),这可能是由于两种多态性之间存在高度连锁不平衡。
我们的研究结果支持以下假设,即rs35569394的D等位基因和DD基因型对DR的进展具有有害影响。由于C等位基因(rs699947)和D等位基因(rs35569394)之间存在强连锁不平衡,C等位基因在DR III受试者中的频率偏高。