首页> 外文期刊>Diabetologia >Association of the SLC30A8 missense polymorphism R325W with proinsulin levels at baseline and after lifestyle, metformin or troglitazone intervention in the Diabetes Prevention Program
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Association of the SLC30A8 missense polymorphism R325W with proinsulin levels at baseline and after lifestyle, metformin or troglitazone intervention in the Diabetes Prevention Program

机译:SLC30A8错义多态性R325W与基线和生活方式,二甲双胍或曲格列酮干预糖尿病及基线后胰岛素水平的相关性

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Individuals with impaired glucose tolerance have increased proinsulin levels, despite normal glucose or C-peptide levels. In the Diabetes Prevention Program (DPP), increased proinsulin levels predicted type 2 diabetes and proinsulin levels were significantly reduced following treatment with metformin, lifestyle modification or troglitazone compared with placebo. Genetic and physiological studies suggest a role for the zinc transporter gene SLC30A8 in diabetes risk, possibly through effects on insulin-processing in beta cells. We hypothesised that the risk allele at the type 2 diabetes-associated missense polymorphism rs13266634 (R325W) in SLC30A8 would predict proinsulin levels in individuals at risk of type 2 diabetes and may modulate response to preventive interventions.
机译:尽管葡萄糖或C肽水平正常,但糖耐量受损的个体的胰岛素原水平却升高。在糖尿病预防计划(DPP)中,与安慰剂相比,二甲双胍,生活方式改变或曲格列酮治疗后,胰岛素原水平的升高预测2型糖尿病和胰岛素原水平显着降低。遗传和生理学研究表明,锌转运蛋白基因SLC30A8在糖尿病风险中的作用可能是通过影响β细胞中胰岛素的加工来实现的。我们假设SLC30A8中2型糖尿病相关错义多态性rs13266634(R325W)的风险等位基因将预测处于2型糖尿病风险的个体的胰岛素原水平,并可能调节对预防干预的反应。

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