【PPARG2基因rs1801282位点变异与糖尿病肾病的关系】。

Genetika Pub Date : 2016-08-01
D Sh Avzaletdinova, L F Sharipova, O V Kochetova, T V Morugova, V V Erdman, O E Mustafina
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引用次数: 0

摘要

分析了巴什科尔托斯坦共和国居民PPARG2基因(过氧化物酶体增殖物激活受体γ)变异位点rs1801282与2型糖尿病及其并发症的关系。在所有三种考虑的遗传模型(共显性、显性和隐性)中,PPARG2基因可变rs1801282位点的基因型频率在健康人组和2型糖尿病患者组中没有显著差异。同时证明糖尿病并发症之一糖尿病肾病的发生风险与PPARG2基因的可变位点rs1801282相关。C/C基因型患者糖尿病肾病发生率(62.7%)高于C/G和G/G基因型患者(37.5%),P = 0.036。G等位基因对2型糖尿病患者的糖尿病肾病具有保护作用(OR = 0.36)。
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[Association of variable rs1801282 locus of PPARG2 gene with diabetic nephropathy].

The association of the variable rs1801282 locus of the PPARG2 gene (peroxisome proliferator-activated receptor gamma) with type 2 diabetes mellitus and its complications was analyzed in inhabitants of the Republic of Bashkortostan. The genotype frequencies of the variable rs1801282 locus of the PPARG2 gene did not significantly differ in groups of healthy persons and patients with type 2 diabetes in all three considered inheritance models (codominant, dominant, and recessive). At the same time, it was demonstrated that the risk of one of the diabetic complications, i.e., diabetic nephropathy, was associated with the variable rs1801282 locus of the PPARG2 gene. Diabetic nephropathy was more common in patients with the C/C genotype (62.7%) compared to the C/G and G/G genotypes (37.5%), P = 0.036. The G allele is protective in regard to diabetic nephropathy (OR = 0.36) in patients with type 2 diabetes mellitus.

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