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特定人类白细胞抗原DQ对胰岛自身抗体表达及1型糖尿病进展的影响。

Specific human leukocyte antigen DQ influence on expression of antiislet autoantibodies and progression to type 1 diabetes.

作者信息

Redondo Maria J, Babu Sunanda, Zeidler Adina, Orban Tihamer, Yu Liping, Greenbaum Carla, Palmer Jerry P, Cuthbertson David, Eisenbarth George S, Krischer Jeffrey P, Schatz Desmond

机构信息

Department of Endocrinology, University Clinic of Navarra, 31008 Pamplona, Spain.

出版信息

J Clin Endocrinol Metab. 2006 May;91(5):1705-13. doi: 10.1210/jc.2005-1695. Epub 2006 Feb 7.

Abstract

CONTEXT

Human leukocyte antigen (HLA) DQ haplotypes have the strongest genetic association with type 1 diabetes (T1DM) risk.

OBJECTIVE

The objective of the study was to analyze whether HLA DQ alleles influence the development of antiislet autoantibodies, the progression to T1DM among autoantibody-positive relatives, or both.

DESIGN

The Diabetes Prevention Trial-1 screened more than 90,000 nondiabetic relatives of patients for cytoplasmic islet-cell autoantibody (ICA) expression between 1994 and 2002.

SETTING

The study was conducted in the general community.

PARTICIPANTS

The Diabetes Prevention Trial-1 found 2817 ICA-positive relatives who were tested for biochemical autoantibodies (GAD65, ICA512, and insulin) and HLA-DQ haplotypes, and 2796 of them were followed up for progression to diabetes for up to 8 yr (median, 3.6 yr).

MAIN OUTCOME MEASURE

Progression to T1DM was measured.

RESULTS

High-risk DQ haplotypes and genotypes were associated with a higher percentage of relatives expressing multiple biochemical autoantibodies and higher T1DM risk (e.g., respectively, 59 and 36% at 5 yr for carriers of the DQA10301-DQB10302/DQA10501-DQB10201 genotype). The number of autoantibodies expressed significantly increased T1DM risk and across different DQ genotypes, autoantibody positivity directly correlated with diabetes risk. However, multivariate analyses indicated that the influence of most genotypes on T1DM risk was not independent from autoantibody expression, with the possible exception of DQA10102-DQB10602. Specific genotypic combinations conferred 5-yr diabetes risks significantly lower (e.g. 7%-DQA10201-DQB10201/DQA10501-DQB10201 and 14%-DQA10301-DQB10301/DQA10501-DQB10201) than when those haplotypes were found in other combinations.

CONCLUSION

HLA DQ alleles determine autoantibody expression, which is correlated with diabetes progression. Among autoantibody-positive relatives, most HLA DQ genotypes did not further influence T1DM risk.

摘要

背景

人类白细胞抗原(HLA)DQ单倍型与1型糖尿病(T1DM)风险具有最强的遗传关联。

目的

本研究的目的是分析HLA DQ等位基因是否影响抗胰岛自身抗体的产生、自身抗体阳性亲属中T1DM的进展,或两者皆有影响。

设计

糖尿病预防试验-1在1994年至2002年期间对90000多名患者的非糖尿病亲属进行了细胞质胰岛细胞自身抗体(ICA)表达筛查。

地点

研究在普通社区进行。

参与者

糖尿病预防试验-1发现2817名ICA阳性亲属,对其进行了生化自身抗体(GAD65、ICA512和胰岛素)及HLA-DQ单倍型检测,其中2796人随访了长达8年的糖尿病进展情况(中位数为3.6年)。

主要观察指标

测量T1DM的进展情况。

结果

高危DQ单倍型和基因型与表达多种生化自身抗体的亲属比例较高以及T1DM风险较高相关(例如,对于DQA10301-DQB10302/DQA10501-DQB10201基因型携带者,5年时分别为59%和36%)。所表达的自身抗体数量显著增加T1DM风险,并且在不同的DQ基因型中,自身抗体阳性与糖尿病风险直接相关。然而,多变量分析表明,大多数基因型对T1DM风险的影响并非独立于自身抗体表达,DQA10102-DQB10602可能除外。特定的基因型组合使5年糖尿病风险显著降低(例如,7%-DQA10201-DQB10201/DQA10501-DQB10201和14%-DQA10301-DQB10301/DQA10501-DQB0201),低于这些单倍型在其他组合中的情况。

结论

HLA DQ等位基因决定自身抗体表达,而自身抗体表达与糖尿病进展相关。在自身抗体阳性亲属中,大多数HLA DQ基因型并未进一步影响TIDM风险。

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