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糖尿病视网膜病变:南印度队列中ALR2、RAGE、iNOS和TNFB基因变异的验证研究。

Diabetic retinopathy: Validation study of ALR2, RAGE, iNOS and TNFB gene variants in a south Indian cohort.

作者信息

Uthra Satagopan, Raman Rajiv, Mukesh Bickol N, Rajkumar Samuel A, Kumari Padmaja, Lakshmipathy Praveena, Gnanamoorthy Perumal, Sharma Tarun, McCarty Catherine A, Kumaramanickavel Govindasamy

机构信息

SN ONGC Department of Genetics and Molecular Biology, Medical and Vision Research Foundations, Sankara Nethralaya, Chennai, India.

出版信息

Ophthalmic Genet. 2010 Dec;31(4):244-51. doi: 10.3109/13816810.2010.523037.

Abstract

PURPOSE

We previously reported the association of the Z-2 allele of the promoter dinucleotide repeat in the Aldose reductase (ALR2) gene, the (CCTTT)₁₅ allele in the promoter of inductible nitric oxide synthase (iNOS) gene, and the (GT)₁₃ promoter polymorphism in the tumor necrosis factor β (TNFB) gene with an increased risk for diabetic retinopathy (DR), and the Gly82Ser polymorphism in the receptor for advanced glycation end products (RAGE) gene and the (GT)₉ allele of the TNFB gene with low-risk for DR in a hospital-based self-reported type 2 diabetes mellitus (T2DM) patients. We have repeated the study in a population-based south Indian cohort to validate the same variations in these genes.

MATERIALS AND METHODS

Type 2 diabetic patients with and without retinopathy (DR+ and DR- respectively) were recruited. (CA)(n) repeat, Gly82Ser, (CCTTT)(n) repeat and (GT)(n) repeat in ALR2, RAGE, iNOS and TNFB genes respectively were genotyped and their frequencies were analyzed using the relevant statistical tests.

RESULTS

Different allelic associations were observed in the present study as compared to our previous reports. Z+2 allele of ALR2, 13-repeat genotype of iNOS, 15-repeat genotype of TNF-β, genes were associated with susceptibility to DR. Gly82Ser polymorphisms of the RAGE gene were not associated with DR in the present study.

CONCLUSION

The present data show a difference in the association of variations in ALR2, iNOS and TNFB genes with DR, when compared to our previous reports; this could be attributed to differences between the study populations of the past and present report.

摘要

目的

我们之前报道过,醛糖还原酶(ALR2)基因启动子二核苷酸重复序列的Z-2等位基因、诱导型一氧化氮合酶(iNOS)基因启动子的(CCTTT)₁₅等位基因以及肿瘤坏死因子β(TNFB)基因启动子的(GT)₁₃多态性与糖尿病视网膜病变(DR)风险增加相关,而晚期糖基化终产物受体(RAGE)基因的Gly82Ser多态性以及TNFB基因的(GT)₉等位基因与以医院为基础的自报2型糖尿病(T2DM)患者的DR低风险相关。我们在一个基于人群的南印度队列中重复了该研究,以验证这些基因中的相同变异。

材料与方法

招募有和没有视网膜病变的2型糖尿病患者(分别为DR+和DR-)。分别对ALR2、RAGE、iNOS和TNFB基因中的(CA)(n)重复、Gly82Ser、(CCTTT)(n)重复和(GT)(n)重复进行基因分型,并使用相关统计检验分析其频率。

结果

与我们之前的报告相比,本研究观察到了不同的等位基因关联。ALR2的Z+2等位基因、iNOS的13重复基因型、TNF-β的15重复基因型与DR易感性相关。本研究中,RAGE基因的Gly82Ser多态性与DR无关。

结论

与我们之前的报告相比,本数据显示ALR2、iNOS和TNFB基因变异与DR的关联存在差异;这可能归因于过去和现在报告的研究人群之间的差异。

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