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伊朗2型糖尿病微血管病变患者醛糖还原酶C-106T基因多态性

Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals.

作者信息

Rezaee Majid Reza Sheikh, Amiri Ahmad Ahmadzadeh, Hashemi-Soteh Mohammad Bagher, Daneshvar Fatemeh, Emady-Jamaly Roghaye, Jafari Reza, Soleimani Behyar, Haghiaminjan Hamed

机构信息

Bu Ali-Sina Clinical Research Development Unit, Mazandaran University of Medical Sciences, Mazandaran, Sari, Iran.

Molecular and Cell Biology Research Center and Medical Faculty, Mazandaran University of Medical Sciences, Mazandaran, Sari, Iran.

出版信息

Indian J Endocrinol Metab. 2015 Jan-Feb;19(1):95-9. doi: 10.4103/2230-8210.131762.

Abstract

BACKGROUND

Aldose reductase (AR) is the rate-limiting enzyme in the glucose metabolism, which has been implicated in the pathogenesis of diabetic microvascular complications (MVCs). Frequent C-106T polymorphism in the promoter of the AR gene may change the expression of the gene.

AIMS

The aim of the following study is to study the association between AR C106T genotypes and diabetic MVCs in Iranian population.

MATERIALS AND METHODS

We included 206 type 2 diabetic patients categorized into two groups according to the presence or absence of diabetic microangiopathy. The cases of interest were diabetic neuropathy, retinopathy and nephropathy identified during clinical and or laboratory examination. In addition, 114 age- and sex-matched individuals were selected to serve as a control group. AR genotyping was done using an amplification gel electrophoresis.

RESULTS

The frequency of CC genotype was specifically higher in subjects with diabetic retinopathy as compared to those without it (53.2% vs. 38.1%, P = 0.030). Patients with diabetic microangiopathy in general; however, did not differ significantly between AR genotype groups.

CONCLUSION

The C-106T polymorphism in the AR gene is likely a risk factor for development of only retinal complication of diabetes microvascular in Iranian individuals.

摘要

背景

醛糖还原酶(AR)是葡萄糖代谢中的限速酶,与糖尿病微血管并发症(MVCs)的发病机制有关。AR基因启动子区域常见的C-106T多态性可能会改变该基因的表达。

目的

本研究旨在探讨伊朗人群中AR C106T基因型与糖尿病MVCs之间的关联。

材料与方法

我们纳入了206例2型糖尿病患者,根据是否存在糖尿病微血管病变分为两组。感兴趣的病例为临床和/或实验室检查中确诊的糖尿病神经病变、视网膜病变和肾病。此外,选取114名年龄和性别匹配的个体作为对照组。采用扩增凝胶电泳法进行AR基因分型。

结果

与无糖尿病视网膜病变的患者相比,糖尿病视网膜病变患者中CC基因型的频率显著更高(53.2%对38.1%,P = 0.030)。然而,总体上糖尿病微血管病变患者在AR基因型组之间无显著差异。

结论

在伊朗人群中,AR基因的C-106T多态性可能是糖尿病微血管仅视网膜并发症发生的危险因素。

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