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胰岛素依赖型糖尿病中的人类白细胞抗原-DR与胰岛素基因5'端多态性

HLA-DR and the 5' insulin gene polymorphism in insulin-dependent diabetes.

作者信息

Raffel L J, Vadheim C M, Klein R, Moss S E, Riley W J, Maclaren N K, Rotter J I

机构信息

Department of Pediatrics, University of Maryland School of Medicine, Baltimore.

出版信息

Metabolism. 1991 Dec;40(12):1244-8. doi: 10.1016/0026-0495(91)90023-p.

Abstract

While the human leukocyte antigen (HLA) region provides the major susceptibility for insulin-dependent (type I) diabetes mellitus (IDDM), other (non-HLA) genes must also play a role. Population studies have shown an increased frequency of small insertions (class I alleles) 5' to the insulin gene in individuals with IDDM, suggesting that this region may account for part, if not all, of the non-HLA genetic predisposition. However, no data are available as to whether the relation of the insulin gene polymorphism is to a DR-defined subset of IDDM or with all of IDDM. To test the hypothesis that specific combinations of HLA and insulin gene polymorphism alleles may interact in providing susceptibility for IDDM, HLA-DR and 5' insulin gene insertion size have been determined in 300 individuals with IDDM. The frequency of class 1 insulin gene alleles in the entire sample is 0.79 and the frequency of class 3 alleles (large inserts) is 0.20. The frequencies of class 1 alleles were equal across all DR classes: 0.79 in the DR3/X IDDM subjects, 0.80 in the DR4/X, 0.79 in the DR3/4, and 0.78 in those with DRX/X. Additionally, the frequencies of class 1/1 homozygotes and 1/3 heterozygotes were similar between HLA-DR types. These results suggest that the HLA region and the region 5' to the insulin gene provide independent and nonsynergistic genetic risks for IDDM.

摘要

虽然人类白细胞抗原(HLA)区域是胰岛素依赖型(I型)糖尿病(IDDM)的主要易感因素,但其他(非HLA)基因也必定发挥作用。人群研究显示,IDDM患者中胰岛素基因5'端小插入(I类等位基因)的频率增加,提示该区域可能至少部分地解释了非HLA遗传易感性。然而,关于胰岛素基因多态性与DR定义的IDDM亚组或所有IDDM之间的关系尚无数据。为了检验HLA和胰岛素基因多态性等位基因的特定组合可能相互作用导致IDDM易感性增加这一假说,我们测定了300例IDDM患者的HLA-DR和胰岛素基因5'端插入大小。整个样本中I类胰岛素基因等位基因的频率为0.79,III类等位基因(大插入)的频率为0.20。所有DR类别中I类等位基因的频率相等:DR3/X IDDM患者中为0.79,DR4/X中为0.80,DR3/4中为0.79,DRX/X患者中为0.78。此外,HLA-DR类型之间I/1纯合子和I/3杂合子的频率相似。这些结果提示,HLA区域和胰岛素基因5'端区域为IDDM提供了独立且非协同的遗传风险。

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