同卵三胞胎的1型糖尿病和糖尿病前期状态。

M Krokowski, M Abel, A Teodorczyk, A Szadkowska, B Pyrzak, B Rymkiewicz-Kluczyńska, J Bodalski
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引用次数: 1

摘要

1型糖尿病(IDDM)是由朗格汉斯胰岛β细胞自身免疫破坏的慢性过程引起的。血清中自身抗体(ICA、GADA、抗ia2、IAA)的存在先于疾病的临床发病。IDDM的遗传易感性与HLA、CTLA-4和胰岛素基因区有关。该研究的目的是对三胞胎进行遗传和免疫学分析。其中一人患上了1型糖尿病。我们分析了整个家族HLAⅱ类、CTLA-4和胰岛素基因多态性。此外,我们还调查了三兄弟的免疫状况。所有患者的VNTR基因座:D1S80、D17S5和载脂蛋白B,以及HLA-DRB1、-DQA1、-DQB1、CTLA-4基因均具有相同的基因型,所有研究的胰岛素基因多态性均相同。这证明了它们的单一性。三胞胎表现出强烈的IDDM遗传易感性。2例无明显糖尿病的患者ICA、GADA、IA2和IAA水平均升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Type 1 diabetes and prediabetic state in a monozygotic triplet.

Type 1 diabetes mellitus (IDDM) results from a chronic process of autoimmune destruction of beta cells of the Langerhans islets. The presence of autoantibodies (ICA, GADA, anti-IA2, IAA) in serum precedes the clinical onset of the disease. Genetic predisposition for IDDM is connected with HLA, CTLA-4 and insulin gene region. The aim of the study was the genetic and immunological analysis of a triplet. One of them developed Type 1 diabetes mellitus. We analysed HLA class II, CTLA-4 and insulin gene polymorphisms in the whole family. Besides, we investigated immunological status of three brothers. All patients present identical genotype for VNTR loci: D1S80, D17S5 and Apo B, as well as for HLA-DRB1, -DQA1, -DQB1, CTLA-4 gene and all studied insulin gene polymorphisms. That proves their monozigosity. The triplet presents strong genetic predisposition for IDDM. The two patients without overt diabetes have increased levels of ICA, GADA, IA2 and IAA.

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