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首页> 外文期刊>Molecular genetics and metabolism >The -106CC genotype of the aldose reductase gene is associated with an increased risk of proliferative diabetic retinopathy in Caucasian-Brazilians with type 2 diabetes.
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The -106CC genotype of the aldose reductase gene is associated with an increased risk of proliferative diabetic retinopathy in Caucasian-Brazilians with type 2 diabetes.

机译:醛糖还原酶基因的-106CC基因型与患有2型糖尿病的高加索巴西人糖尿病性增生性视网膜病变的风险增加相关。

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Diabetic retinopathy is a sight-threatening chronic complication of diabetes mellitus and is the leading cause of acquired blindness in adults. The -106C>T polymorphism in the promoter region of the aldose reductase (AR) gene has been shown to be associated with the susceptibility to diabetic nephropathy in type 2 diabetes, but the findings regarding the occurrence of diabetic retinopathy are conflicting. In this case-control study, we investigated whether the -106C>T polymorphism in the AR gene is involved in the development and progression of diabetic retinopathy in 579 Brazilians with type 2 diabetes (424 Caucasian- and 155 African-Brazilians). Patients underwent a clinical and laboratory evaluation consisting of a questionnaire, physical examination, assessment of diabetic complications and laboratory tests. Genotype analysis was performed using the polymerase chain reaction followed by digestion with restriction enzyme. Logistic regression analysis was used to control for independent risk factors associated with diabetic retinopathy. There were no differences in either genotype or allele frequencies for the -106C>T polymorphism between type 2 diabetic patients with or without diabetic retinopathy, in both ethnic groups. However, the CC genotype was associated with an increased risk of having proliferative diabetic retinopathy in Caucasian-Brazilians with type 2 diabetes (odds ratio (OR)=2.04; 95% confidence interval (CI)=1.21-3.45; P=0.007), independently of other risk factors associated with this complication. Thus, our results show that the -106CC genotype (-106C>T polymorphism) in the AR gene is related to the progression of diabetic retinopathy in Caucasian-Brazilians with type 2 diabetes.
机译:糖尿病性视网膜病是威胁视力的慢性糖尿病并发症,是成人获得性失明的主要原因。醛糖还原酶(AR)基因启动子区域的-106C> T多态性已被证明与2型糖尿病对糖尿病肾病的易感性有关,但有关糖尿病性视网膜病发生的发现存在矛盾。在本病例对照研究中,我们调查了579名2型糖尿病巴西人(424名白种人和155名非洲巴西人)中AR基因中的-106C> T多态性是否与糖尿病性视网膜病变的发生和发展有关。患者接受了临床和实验室评估,包括问卷调查,体格检查,糖尿病并发症评估和实验室检查。使用聚合酶链反应进行基因型分析,然后用限制酶消化。 Logistic回归分析用于控制与糖尿病性视网膜病变相关的独立危险因素。在两个种族中,有或没有糖尿病视网膜病变的2型糖尿病患者之间-106C> T多态性的基因型或等位基因频率均无差异。然而,CC基因型与患有2型糖尿病的白种人-巴西人罹患增生性糖尿病视网膜病变的风险增加相关(比值比(OR)= 2.04; 95%置信区间(CI)= 1.21-3.45; P = 0.007),独立于与此并发症相关的其他风险因素。因此,我们的结果表明,AR基因中的-106CC基因型(-106C> T多态性)与2型糖尿病高加索巴西人糖尿病性视网膜病变的进展有关。

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