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南亚人2型糖尿病早发及进展的遗传基础。

Genetic basis of early onset and progression of type 2 diabetes in South Asians.

作者信息

Hodgson Sam, Williamson Alice, Bigossi Margherita, Stow Daniel, Jacobs Benjamin M, Samuel Miriam, Gafton Joseph, Zöllner Julia, Spreckley Marie, Langenberg Claudia, van Heel David A, Mathur Rohini, Siddiqui Moneeza K, Finer Sarah

机构信息

Wolfson Institute of Population Health, Queen Mary University of London, London, UK.

Precision Healthcare University Research Institute, Queen Mary University of London, London, UK.

出版信息

Nat Med. 2025 Jan;31(1):323-331. doi: 10.1038/s41591-024-03317-8. Epub 2024 Nov 26.

Abstract

South Asians develop type 2 diabetes (T2D) early in life and often with normal body mass index (BMI). However, reasons for this are poorly understood because genetic research is largely focused on European ancestry groups. We used recently derived multi-ancestry partitioned polygenic scores (pPSs) to elucidate underlying etiological pathways British Pakistani and British Bangladeshi individuals with T2D (n = 11,678) and gestational diabetes mellitus (GDM) (n = 1,965) in the Genes & Health study (n = 50,556). Beta cell 2 (insulin deficiency) and Lipodystrophy 1 (unfavorable fat distribution) pPSs were most strongly associated with T2D, GDM and younger age at T2D diagnosis. Individuals at high genetic risk of both insulin deficiency and lipodystrophy were diagnosed with T2D 8.2 years earlier with BMI 3 kg m lower compared to those at low genetic risk. The insulin deficiency pPS was associated with poorer HbA1c response to SGLT2 inhibitors. Insulin deficiency and lipodystrophy pPSs were associated with faster progression to insulin dependence and microvascular complications. South Asians had a greater genetic burden from both of these pPSs than white Europeans in the UK Biobank. In conclusion, genetic predisposition to insulin deficiency and lipodystrophy in British Pakistani and British Bangladeshi individuals is associated with earlier onset of T2D, faster progression to complications, insulin dependence and poorer response to medication.

摘要

南亚人在年轻时就会患上2型糖尿病(T2D),而且通常体重指数(BMI)正常。然而,人们对其原因了解甚少,因为基因研究主要集中在欧洲血统群体上。在“基因与健康”研究(n = 50,556)中,我们使用最近得出的多血统分区多基因评分(pPSs)来阐明患有T2D(n = 11,678)和妊娠糖尿病(GDM)(n = 1,965)的英国巴基斯坦人和英国孟加拉国人的潜在病因途径。β细胞2(胰岛素缺乏)和脂肪营养不良1(不利的脂肪分布)pPSs与T2D、GDM以及T2D诊断时的年轻年龄关联最为密切。与低遗传风险个体相比,胰岛素缺乏和脂肪营养不良遗传风险高的个体被诊断为T2D的时间要早8.2年,BMI低3 kg/m²。胰岛素缺乏pPS与对SGLT2抑制剂的糖化血红蛋白反应较差有关。胰岛素缺乏和脂肪营养不良pPSs与更快进展为胰岛素依赖和微血管并发症有关。在英国生物银行中,南亚人这两种pPSs的遗传负担比白人欧洲人更大。总之,英国巴基斯坦人和英国孟加拉国人胰岛素缺乏和脂肪营养不良的遗传易感性与T2D发病更早、并发症进展更快、胰岛素依赖以及药物反应较差有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fce/11750703/007bcf5d3767/41591_2024_3317_Fig1_HTML.jpg

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