瘦素受体rs1137101基因多态性对2型糖尿病和肥胖症发生的影响

Ziablitsev Sv
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引用次数: 2

摘要

本研究的目的是研究LEPR基因多态性rs1137101在2型糖尿病发展中的作用及其对这些患者肥胖相关临床和实验室数据的影响。103名患者接受了检查,这些患者有临床表现出的并发症。对照组由100名相应年龄的实际健康人组成。多态性DNA位点的分析是通过聚合酶链式反应的方法实时进行的(TaqMan®SNP基因分型测定)。结果表明,rs1137101等位基因多态性(223Gln>Arg)与2型糖尿病的发生有关:等位基因Gln促进糖尿病的发生,而等位基因Arg降低糖尿病的发生风险(OR=1.5;P=0.039)。糖尿病患者的存在等位基因Gln有助于肥胖的发展和他的表现,即,在高密度脂蛋白维持的背景下,体重指数和HOMA-IR的值更高,瘦素和甘油三酯的血液水平也更高。这些患者患肥胖症的风险增加了1.8倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of rs1137101 gene polymorphism of leptin receptor on the development of diabetes mellitus type 2 and obesity
The aim of this research was a study of gene LEPR polymorphism rs1137101 role in diabetes mellitus 2 type development and his influences on the clinical and laboratory data, related to obesity for these patients. 103 patients are inspected, that had the clinically expressed complications. A control group was made by 100 practically healthy persons of corresponding age. The analysis of polymorphic DNA-loci was carried out by the method of polymerase chain reaction in real time (TaqMan® SNP Genotyping Assay). Results showed that allelic polymorphism of rs1137101 (223Gln>Arg) had been associated with diabetes mellitus 2 types development: allele Gln promotes, while allele Arg – reduces (OR=1.5; P=0.039) the risk of its development. Presence allele Gln for diabetic patients assists development of obesity and his displays, namely – to the higher values of body mass index and HOMA-IR, and also to the greater leptin and triglycerides blood levels on a background reduction of high-density lipoproteides maintenance. The risk of developing obesity in these patients is increased by 1.8 times.
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