KCNJ11、ADIPOQ、omentin、leptin、TCF7L2和PPARg基因多态性位点在吉尔吉斯人群2型糖尿病发病中的相互作用和贡献:一项使用MDR分析的病例对照遗传关联研究

Zh. T. Isakova, E. Talaibekova, Baktygul Zh. Zhyrgalbekova, E. Mirrakhimov, N. Aldasheva, A. Aldashev
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引用次数: 3

摘要

有许多与2型糖尿病(T2DM)相关的基因位点。参与T2DM发展的遗传因素可能取决于不同种族群体内部和之间遗传变异的性质。目的-本研究的目的是研究基因-基因相互作用,并确定KCNJ11 (Glu23Lys), ADIPOQ (G276T), omentin (Val109Asp), leptin (G2548A), TCF7L2 (IVS3C/T), PPARg (Pro12Ala)基因在吉尔吉斯斯坦人群2型糖尿病(T2DM)发展中的作用。材料和方法。我们检查了114例患者(女性53例,男性61例;平均年龄(54±7.4)岁,正常对照109例(女性48例,男性61例;平均年龄(50±8.4)。采用PCR-RFLP法确定了KCNJ11 (Glu23Lys)、ADIPOQ (G276T)、omentin (Val109Asp)、leptin (G2548A)、TCF7L2 (IVS3C/T)、ppar (Pro12Ala)基因的多态性。结果。在本研究纳入的6个基因(KCNJ11、ADIPOQ、omentin、leptin、TCF7L2、PPARg)中,检测到ADIPOQ(2.17%)和KCNJ11基因(2.01%)对吉尔吉斯斯坦人群T2DM的发展贡献最大。杂合子基因型G276T (OR=1.79 CI 95% 1.05-3.05;p=0.036)和276T等位基因(OR=1.68 CI 95% 1.09-2.60;p=0.025)的ADIPOQ基因与吉尔吉斯斯坦人群中发生T2DM的高风险相关。KCNJ11基因的23Lys等位基因与吉尔吉斯人群的T2DM显著相关(OR=1.62 CI 95% 1.10-2.38;p = 0.019)。大网膜蛋白(Val109Asp)、瘦素(G2548A)、TCF7L2 (IVS3C/T)、PPARg (Pro12Ala)基因等位基因频率和基因型频率在两组间无显著差异(p>0.05)。结论。在吉尔吉斯人群中,KCNJ11基因的多态位点Glu23Lys、ADIPOQ的276T等位基因和基因型G276T与T2DM相关。单独的omentin (Val109Asp)、leptin (G2548A)、TCF7L2 (IVS3C/T)和PPARg (Pro12Ala)基因对2型糖尿病的发展没有如此显著的影响;它们主要通过基因-基因相互作用促进T2DM的表型发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene-gene interactions and the contribution of polymorphic loci of the KCNJ11, ADIPOQ, omentin, leptin, TCF7L2 and PPARg genes to the development of type 2 diabetes mellitus in the Kyrgyz population: a case-control genetic association study using MDR analysis
There are many genetic loci associated with type 2 diabetes mellitus (T2DM). The genetic factors involved in the development of the T2DM can depend on the nature of genetic variation within and across different ethnic groups. Aims — the aim of this study was to investigate the gene-gene interactions and to determine the role of the KCNJ11 (Glu23Lys), ADIPOQ (G276T), omentin (Val109Asp), leptin (G2548A), TCF7L2 (IVS3C/T), PPARg (Pro12Ala) genes in the development of type 2 diabetes mellitus (T2DM) in the Kyrgyz population using MDR analysis. Material and methods. We examined 114 patients (53 females and 61 males; mean age, 54±7.4) with T2DM and 109 apparently healthy controls (48 females and 61 males; mean age, 50±8.4). Polymorphisms of the KCNJ11 (Glu23Lys), ADIPOQ (G276T), omentin (Val109Asp), leptin (G2548A), TCF7L2 (IVS3C/T), PPARg (Pro12Ala) genes were defined by PCR-RFLP assay. Results. Among the six genes (KCNJ11, ADIPOQ, omentin, leptin, TCF7L2, PPARg) included in this study, the most significant contribution to the development of T2DM in the Kyrgyz population was detected for the ADIPOQ (2.17%) and KCNJ11 genes (2.01%). The heterozygous genotype G276T (OR=1.79 CI 95% 1.05—3.05; p=0.036) and the 276T allele (OR=1.68 CI 95% 1.09—2.60; p=0.025) of the ADIPOQ gene were associated with a high risk of developing T2DM in the Kyrgyz population. The 23Lys allele of the KCNJ11 gene was significantly associated with T2DM in the Kyrgyz population (OR=1.62 CI 95% 1.10—2.38; p=0.019). The allele and genotype frequencies of the omentin (Val109Asp), leptin (G2548A), TCF7L2 (IVS3C/T), PPARg (Pro12Ala) genes did not differ between the studied groups (p>0.05). Conclusions. In Kyrgyz population, the polymorphic loci Glu23Lys of the KCNJ11 gene, the 276T allele and genotype G276T of ADIPOQ are associated with T2DM. The omentin (Val109Asp), leptin (G2548A), TCF7L2 (IVS3C/T), and PPARg (Pro12Ala) genes alone do not have such a significant impact on the development of type 2 diabetes; they contribute to the phenotypic development of T2DM mainly due to gene-gene interactions.
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