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对非裔美国 1 型糖尿病患者的 HLA Ⅱ类基因分型揭示了仅存在于非洲单倍型中的关联。

HLA class II genotyping of African American type 1 diabetic patients reveals associations unique to African haplotypes.

机构信息

Children's Hospital Oakland Research Institute, Oakland, California, USA.

出版信息

Diabetes. 2013 Sep;62(9):3292-9. doi: 10.2337/db13-0094. Epub 2013 Jun 25.

DOI:10.2337/db13-0094
PMID:23801574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3749336/
Abstract

HLA genotyping was performed in African American type 1 diabetic patients (n = 772) and controls (n = 1,641) in the largest study of African Americans and type 1 diabetes reported to date. Cases were from Children's Hospital and Research Center Oakland and from existing collections (Type 1 Diabetes Genetics Consortium [T1DGC], Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications [DCCT/EDIC], and Genetics of Kidneys in Diabetes [GoKinD]). Controls were from the T1DGC and from newborn bloodspot cards. The diversity of HLA DRB1-DQA1-DQB1 haplotypes and genotypes is far greater than that found in Europeans and European Americans. Association analyses replicated many type 1 diabetes risk effects of European-derived haplotypes but also revealed novel effects for African-derived haplotypes. Notably, the African-specific "DR3" haplotype DRB103:02-DQA104:01-DQB104:02 is protective for type 1 diabetes, in contrast to the common and highly-susceptible DR3 DRB103:01-DQA105:01-DQB102:01. Both DRB107:01 and DRB113:03 haplotypes are predisposing when they include DQA103:01-DQB102:01g but are protective with DQA102:01-DQB102:01g. The heterozygous DR4/DR9 genotype, containing the African-derived "DR9" haplotype DRB109:01-DQA103:01-DQB1*02:01g, exhibits extremely high risk (odds ratio = 30.88), approaching that for DR3/DR4 in European populations. Disease risk assessment for African Americans differs greatly from risk assessment in European populations. This has profound implications on risk screening programs and underscores the need for high-resolution genotyping of multiple populations for the rational design of screening programs with tests that will fairly represent the population being screened.

摘要

HLA 基因分型在迄今为止报道的最大的非裔美国 1 型糖尿病患者(n = 772)和对照(n = 1641)中进行。病例来自奥克兰儿童医院和研究中心,以及现有的收集(1 型糖尿病遗传学联合会 [T1DGC]、糖尿病控制和并发症试验/糖尿病干预和并发症的流行病学 [DCCT/EDIC]和糖尿病肾脏遗传学 [GoKinD])。对照来自 T1DGC 和新生儿血斑卡。HLA DRB1-DQA1-DQB1 单倍型和基因型的多样性远远大于欧洲人和欧洲裔美国人。关联分析复制了许多欧洲来源单倍型的 1 型糖尿病风险效应,但也揭示了非洲来源单倍型的新效应。值得注意的是,非洲特异性的“DR3”单倍型 DRB103:02-DQA104:01-DQB104:02 对 1 型糖尿病具有保护作用,与常见的高度易感 DR3 DRB103:01-DQA105:01-DQB102:01 相反。当包含 DQA103:01-DQB102:01g 时,DRB107:01 和 DRB113:03 单倍型都是易感的,但当包含 DQA102:01-DQB102:01g 时,它们是保护性的。杂合的 DR4/DR9 基因型,包含非洲来源的“DR9”单倍型 DRB109:01-DQA103:01-DQB1*02:01g,表现出极高的风险(比值比=30.88),接近欧洲人群中的 DR3/DR4。非裔美国人的疾病风险评估与欧洲人群的风险评估有很大的不同。这对风险筛查计划有深远的影响,并强调需要对多个人群进行高分辨率基因分型,以便合理设计具有代表性的筛查计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cc2/3749336/53f788c1ac02/3292fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cc2/3749336/53f788c1ac02/3292fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cc2/3749336/53f788c1ac02/3292fig1.jpg

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