Shcherbak N S, Schwartz E I
Laboratory of Molecular Cardiology, St. Petersburg State Medical University, Russia.
J Hum Genet. 2001;46(4):188-91. doi: 10.1007/s100380170087.
Complications of insulin-dependent diabetes mellitus (IDDM) are a major cause of morbidity and mortality; however, the mechanisms of their development are still to be elucidated. Genetic susceptibility contributes to the pathogenesis of nephropathy in IDDM. Enhanced G-protein activation, a cellular phenotype observed in cultured cells from patients with essential hypertension, was recently documented in IDDM subjects with nephropathy. A C825T polymorphism was recently described in GNB3, the gene encoding the beta 3 subunit of heterotrimeric G-proteins. This genetic variant has been associated with enhanced G-protein activation. The 825T allele was observed more frequently in a group with essential hypertension. We analyzed the role of the C825T polymorphism in the predisposition to diabetic complications in IDDM. In this study, we investigated the frequency of this polymorphism in a large case-control study and found no association of the 825T allele with diabetic nephropathy, retinopathy, and neuropathy.
胰岛素依赖型糖尿病(IDDM)的并发症是发病和死亡的主要原因;然而,其发病机制仍有待阐明。遗传易感性在IDDM肾病的发病机制中起作用。增强的G蛋白激活是原发性高血压患者培养细胞中观察到的一种细胞表型,最近在患有肾病的IDDM患者中也有记录。最近在编码异三聚体G蛋白β3亚基的基因GNB3中描述了一种C825T多态性。这种基因变异与增强的G蛋白激活有关。在原发性高血压组中更频繁地观察到825T等位基因。我们分析了C825T多态性在IDDM糖尿病并发症易感性中的作用。在这项研究中,我们在一项大型病例对照研究中调查了这种多态性的频率,发现825T等位基因与糖尿病肾病、视网膜病变和神经病变无关联。