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Chemotactic cytokine receptor 5 gene polymorphism: Relevance to microvascular complications in type 2 diabetes

机译:趋化性细胞因子受体5基因多态性:与2型糖尿病微血管并发症的相关性。

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We investigated the involvement of chemotactic cytokine receptor 5 (CCR5) gene polymorphism in microvascular complications of T2DM. All subjects were genotyped with the 59029 SNP in the CCR5 gene. The genotype/allele frequencies did not differ between T2DM patients and controls. Genotype distribution was compared in patients with and without complications (nephropathy, retinopathy and neuropathy). The frequency of A allele was significantly higher in patients with complications (OR for A allele 3.07, 95% CI 2.49-3.77). The A allele carriage was associated with diabetic nephropathy (OR 6.17, 95% CI 3.28-11.6). An association was observed between 59029 polymorphism and age at T2DM onset. The A allele was more frequent in early onset than in late onset patients. For AA homozygotes OR was 2.38 (1.19-4.76) and 2.26 (1.12-4.58) in complicated and uncomplicated subgroups, respectively. These results suggest that CCR5 gene polymorphism is associated with diabetic nephropathy in T2DM.
机译:我们调查了趋化性细胞因子受体5(CCR5)基因多态性与T2DM微血管并发症的关系。用CCR5基因中的59029 SNP对所有受试者进行基因分型。 T2DM患者和对照组之间的基因型/等位基因频率没有差异。比较有无并发症(肾病,视网膜病和神经病)患者的基因型分布。患有并发症的患者中,A等位基因的频率明显更高(A等位基因为3.07,95%CI为2.49-3.77)。 A等位基因携带者与糖尿病性肾病相关(OR 6.17,95%CI 3.28-11.6)。在T2DM发作时观察到59029多态性与年龄之间存在关联。 A等位基因在发病初期比在发病后期更为频繁。对于AA,纯合子在复杂和非复杂亚组中的OR分别为2.38(1.19-4.76)和2.26(1.12-4.58)。这些结果表明CCR5基因多态性与T2DM中的糖尿病肾病有关。

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