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使用 I 类和 II 类 HLA 基因座预测多个群体 1 型糖尿病的发病年龄。

Use of class I and class II HLA loci for predicting age at onset of type 1 diabetes in multiple populations.

机构信息

Department of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital, London SE1 7EH, UK.

出版信息

Diabetologia. 2012 Sep;55(9):2394-401. doi: 10.1007/s00125-012-2608-z. Epub 2012 Jun 17.

Abstract

AIMS/HYPOTHESIS: The study aimed to assess, in multiple populations, the role of HLA alleles on early and late age at onset of type 1 diabetes.

METHODS

Stepwise linear regression models were used to determine which HLA class I and class II risk alleles to include. High-resolution genotyping data for patients from the Type 1 Diabetes Genetics Consortium (T1DGC) collection (n = 2,278) and four independent cohorts from Denmark, Sardinia and the USA (Human Biological Data Interchange [HBDI] and Joslin Diabetes Center) (n = 1,324) (total n = 3,602) were used to assess the role of HLA variation on age of onset and predict early onset (age ≤ 5 years) and late onset (age ≥ 15 years) of type 1 diabetes.

RESULTS

In addition to carriage of HLA class I alleles A24:02, B39:06, B44:03 and B18:01, HLA class II DRB1-DQB1 loci significantly contributed to age at onset, explaining 3.4% of its variance in the combined data. HLA genotypes, together with sex, were able to predict late onset in all cohorts studied, with AUC values ranging from 0.58 to 0.63. Similar AUC values (0.59-0.70) were obtained for early onset for most cohorts, except in the Sardinian study, in which none of the models tested had significant predictive power.

CONCLUSIONS/INTERPRETATION: HLA associations with age of onset are consistent across most white populations and HLA information can predict some of the risk of early and late onset of type 1 diabetes. Considerable heterogeneity was observed between Sardinian and other populations, particularly with regard to early age of onset.

摘要

目的/假设:本研究旨在评估多种人群中 HLA 等位基因对 1 型糖尿病早发和晚发年龄的作用。

方法

采用逐步线性回归模型来确定包含哪些 HLA Ⅰ类和Ⅱ类风险等位基因。使用来自 1 型糖尿病遗传学联合会(T1DGC)数据集的患者高分辨率基因分型数据(n=2278)和来自丹麦、撒丁岛和美国的四个独立队列(人类生物数据交换[HBDI]和 Joslin 糖尿病中心)(n=1324)(总 n=3602)来评估 HLA 变异对发病年龄的作用,并预测 1 型糖尿病的早发(年龄≤5 岁)和晚发(年龄≥15 岁)。

结果

除了 HLA Ⅰ类等位基因 A24:02、B39:06、B44:03 和 B18:01 的携带外,HLA Ⅱ类 DRB1-DQB1 基因座也显著影响发病年龄,在合并数据中解释了其方差的 3.4%。HLA 基因型与性别一起能够预测所有研究队列的晚发,AUC 值范围为 0.58-0.63。对于大多数队列,早发的 AUC 值(0.59-0.70)也相似,但在撒丁岛研究中,测试的模型均无显著预测能力。

结论/解释:HLA 与发病年龄的关联在大多数白人群体中是一致的,HLA 信息可以预测 1 型糖尿病的早发和晚发风险的一部分。在撒丁岛人群和其他人群之间观察到相当大的异质性,特别是在早发年龄方面。

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