期刊
DIABETOLOGIA
卷 53, 期 11, 页码 2289-2297出版社
SPRINGER
DOI: 10.1007/s00125-010-1876-8
关键词
Diabetes mellitus type 2; GIPR; Glucagon-like peptide-1; Glucose-dependent insulinotropic peptide; Insulin secretion; KCNQ1; Pancreatic beta cell; Review; TCF7L2; WFS1
资金
- German Research Foundation [Fr 1561/5-1]
Recent genome-wide association studies identified several novel risk genes for type 2 diabetes. The majority of these type 2 diabetes risk variants confer impaired pancreatic beta cell function. Though the molecular mechanisms by which common genetic variation within these loci affects beta cell function are not completely understood, risk variants may alter glucose-stimulated insulin secretion, proinsulin conversion, and incretin signals. In humans, the incretin effect is mediated by the secretion and insulinotropic action of two peptide hormones, glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1. This review article aims to give an overview of the type 2 diabetes risk loci that were found to associate with incretin secretion or incretin action, paying special attention to the potential underlying mechanisms.
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