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DRB1*0403可保护具有高危杂合DQA1*0301-DQB1*0302/DQA1*0501-DQB1*0201基因型的白种人预防胰岛素依赖型糖尿病。比利时糖尿病登记处。

DRB1*0403 protects against IDDM in Caucasians with the high-risk heterozygous DQA1*0301-DQB1*0302/DQA1*0501-DQB1*0201 genotype. Belgian Diabetes Registry.

作者信息

Van der Auwera B, Van Waeyenberge C, Schuit F, Heimberg H, Vandewalle C, Gorus F, Flament J

机构信息

Department of Biochemistry, Vrije Universiteit Brussel, Belgium.

出版信息

Diabetes. 1995 May;44(5):527-30. doi: 10.2337/diab.44.5.527.

Abstract

The human leukocyte antigen (HLA) class II genotype DQA10301-DQB10302/DQA10501-DQB10201 has been identified as a marker strongly predisposing to insulin-dependent diabetes mellitus (IDDM) in Caucasian populations. Its frequency in control populations (1-3%) is still, however, 1 order of magnitude higher than the prevalence of IDDM, suggesting that its penetrance can be modified by protective factors. In this study we searched for such a factor in the DRB1 locus by studying DRB104 polymorphism in 174 European Caucasian IDDM patients and 73 nondiabetic control subjects, all sharing the HLA-DR3/DR4 phenotype. Significant protection was encoded by the DRB10403 allele, which was observed in 5 of 49 control subjects (10%) and none of 171 IDDM patients (0%) with the DQA10301-DQB10302/DQA10501-DQB10201 genotype (RR = 0.02 [0.01-0.18], P < 0.0005). These data support the concept that protective HLA class II genes can overrule the risk caused by HLA-DQ susceptibility dimers. They also contribute to a possible strategy to screen for nondiabetic individuals with increased genetic risk of developing IDDM.

摘要

人类白细胞抗原(HLA)II类基因型DQA10301-DQB10302/DQA10501-DQB10201已被确定为白种人群中胰岛素依赖型糖尿病(IDDM)的一个强烈易感标记。然而,其在对照人群中的频率(1%-3%)仍比IDDM的患病率高1个数量级,这表明其外显率可被保护因素所改变。在本研究中,我们通过研究174例欧洲白种IDDM患者和73例非糖尿病对照者(均具有HLA-DR3/DR4表型)的DRB1基因多态性,在DRB1基因座中寻找这样一个因素。DRB10403等位基因具有显著的保护作用,在49例具有DQA10301-DQB10302/DQA10501-DQB1*0201基因型的对照者中有5例(10%)携带该等位基因,而在171例IDDM患者中无1例携带(0%)(相对危险度RR = 0.02 [0.01-0.18],P < 0.0005)。这些数据支持了保护性HLA II类基因可抵消HLA-DQ易感二聚体所带来风险的概念。它们还为筛查具有增加的发生IDDM遗传风险的非糖尿病个体提供了一种可能的策略。

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