Grarup Niels, Moltke Ida, Albrechtsen Anders, Hansen Torben
Section for Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
The Bioinformatics Centre, Department of Biology, University of Copenhagen, 2200 Copenhagen, Denmark.
Rev Diabet Stud. 2015 Fall-Winter;12(3-4):320-9. doi: 10.1900/RDS.2015.12.320. Epub 2016 Feb 10.
Type 2 diabetes (T2D) is an increasing health problem worldwide with particularly high occurrence in specific subpopulations and ancestry groups. The high prevalence of T2D is caused both by changes in lifestyle and genetic predisposition. A large number of studies have sought to identify the genetic determinants of T2D in large, open populations such as Europeans and Asians. However, studies of T2D in population isolates are gaining attention as they provide several advantages over open populations in genetic disease studies, including increased linkage disequilibrium, homogeneous environmental exposure, and increased allele frequency. We recently performed a study in the small, historically isolated Greenlandic population, in which the prevalence of T2D has increased to more than 10%. In this study, we identified a common nonsense variant in TBC1D4, which has a population-wide impact on glucose-stimulated plasma glucose, serum insulin levels, and T2D. The variant defines a specific subtype of non-autoimmune diabetes characterized by decreased post-prandial glucose uptake and muscular insulin resistance. These and other recent findings in population isolates illustrate the value of performing medical genetic studies in genetically isolated populations. In this review, we describe some of the advantages of performing genetic studies of T2D and related cardio-metabolic traits in a population isolate like the Greenlandic, and we discuss potentials and perspectives for future research into T2D in this population.
2型糖尿病(T2D)是一个在全球范围内日益严重的健康问题,在特定亚人群体和血统群体中发病率尤其高。T2D的高患病率是由生活方式的改变和遗传易感性共同导致的。大量研究试图在欧洲人和亚洲人等大型开放人群中确定T2D的遗传决定因素。然而,对人群隔离群体中T2D的研究正受到关注,因为它们在遗传疾病研究中比开放人群具有若干优势,包括连锁不平衡增加、环境暴露同质化以及等位基因频率增加。我们最近在历史上与世隔绝的格陵兰小群体中进行了一项研究,其中T2D的患病率已升至10%以上。在这项研究中,我们在TBC1D4中鉴定出一种常见的无义变异,它对葡萄糖刺激的血浆葡萄糖、血清胰岛素水平和T2D具有全人群影响。该变异定义了一种非自身免疫性糖尿病的特定亚型,其特征为餐后葡萄糖摄取减少和肌肉胰岛素抵抗。人群隔离群体中的这些及其他近期发现说明了在基因隔离人群中开展医学遗传学研究的价值。在这篇综述中,我们描述了在像格陵兰人群这样的隔离群体中对T2D及相关心血管代谢性状进行遗传研究的一些优势,并讨论了该人群中T2D未来研究的潜力和前景。