Department of Preventive Medicine, Keck School of Medicine of USC, Los Angeles, CA 90089-9011, USA.
Curr Diab Rep. 2010 Dec;10(6):476-84. doi: 10.1007/s11892-010-0143-1.
The physiologic hallmarks of type 2 diabetes are insulin resistance in hepatic and peripheral tissues and pancreatic β-cell dysfunction. Thus, genetic loci underlying susceptibility to type 2 diabetes are likely to map to one of these endophenotypes. Genome-wide association studies have now identified up to 38 susceptibility loci for type 2 diabetes and a number of other loci underlying variation in type 2 diabetes-related quantitative traits. The majority are of unknown biology or map to pancreatic β-cell dysfunction. A seemingly disproportionate minority map to insulin resistance. We briefly discuss the known insulin resistance loci identified from genome-wide association, and then discuss reasons why additional insulin resistance loci have not been identified. We present alternative views that may partly explain the apparent dearth of insulin resistance loci contributing to genetic susceptibility to type 2 diabetes, rather than focus on traditional issues such as study design and sampling, which have been addressed elsewhere.
2 型糖尿病的生理特征是肝和外周组织的胰岛素抵抗以及胰岛β细胞功能障碍。因此,易患 2 型糖尿病的遗传位点可能映射到这些表型之一。全基因组关联研究已经确定了多达 38 个 2 型糖尿病易感性位点,以及一些其他与 2 型糖尿病相关定量性状变化相关的位点。大多数是未知生物学的,或者映射到胰岛β细胞功能障碍。一个看似不成比例的少数映射到胰岛素抵抗。我们简要讨论了从全基因组关联中确定的已知胰岛素抵抗位点,然后讨论了为什么没有发现其他胰岛素抵抗位点的原因。我们提出了替代观点,这些观点可能部分解释了导致 2 型糖尿病遗传易感性的胰岛素抵抗位点明显缺乏的原因,而不是像其他地方所讨论的那样,侧重于研究设计和采样等传统问题。