Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, CO, USA.
Arterioscler Thromb Vasc Biol. 2012 Sep;32(9):2091-6. doi: 10.1161/ATVBAHA.112.255463.
This review summarizes the current understanding of the genetic basis of glucose homeostasis through genome-wide association scans and candidate gene studies of case-control and family-based designs. We highlight the implications of phenotype-direct (euglycemic clamp or frequently sampled intravenous glucose tolerance test) and indirect (fasting insulin and fasting glucose) measures on the determinants of insulin resistance and β-cell response that precede and contribute to the development of type 2 diabetes mellitus (T2DM) and the metabolic syndrome. Finally, we examine future approaches that may aid in understanding the biology of insulin resistance and T2DM. Over the past 2 decades, the prevalence of insulin resistance, the metabolic syndrome, and T2DM has increased. Ethnic differences in T2DM and insulin resistance are evident, with nonwhite populations having the greatest risk. There continue to be significant gaps in our knowledge regarding the metabolic, behavioral, and genetic determinants of these conditions. Understanding the genetic basis of glucose homeostasis, insulin resistance, and T2DM should provide insight on known and novel metabolic pathways that identify potential therapeutic targets and mechanisms for intervention.
这篇综述总结了通过全基因组关联扫描和病例对照及基于家族的候选基因研究,对葡萄糖稳态遗传基础的现有认识。我们强调了表型直接(血糖钳夹或频繁采样静脉葡萄糖耐量试验)和间接(空腹胰岛素和空腹血糖)测量对胰岛素抵抗和β细胞反应决定因素的影响,这些因素先于并促成了 2 型糖尿病(T2DM)和代谢综合征的发展。最后,我们研究了未来可能有助于理解胰岛素抵抗和 T2DM 生物学的方法。在过去的 20 年中,胰岛素抵抗、代谢综合征和 T2DM 的患病率有所增加。T2DM 和胰岛素抵抗的种族差异明显,非白人群的风险最大。我们对这些疾病的代谢、行为和遗传决定因素的了解仍然存在很大差距。了解葡萄糖稳态、胰岛素抵抗和 T2DM 的遗传基础,应能深入了解已知和新的代谢途径,从而确定潜在的治疗靶点和干预机制。