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自身免疫性糖尿病的遗传学

Genetics of autoimmune diabetes mellitus.

作者信息

Cerná Marie

机构信息

Department of Cellular and Molecular Biology, Third Faculty of Medicine, Charles University, Ruská 87, Prague, Czech Republic.

出版信息

Wien Med Wochenschr. 2008;158(1-2):2-12. doi: 10.1007/s10354-007-0448-0.

Abstract

Autoimmune diabetes mellitus, called type 1 diabetes mellitus (T1DM), is caused by autoimmune destruction of islet beta cells in the pancreas. T1DM susceptibility loci mapped by different genome screening are IDDM1-IDDM18. It has been estimated that HLA (IDDM1) provides up to 40-50 % of the familial clustering of T1DM (LOD score of 65.8). Many studies have verified that DQB10302 is a strong susceptibility gene and that the heterozygous combination of DQA10301-DQB10302 on the HLA-DR4 haplotype and DQA10501-DQB1*0201 on the HLA-DR3 haplotype results in a synergistically increased risk of T1DM. The presence of predisposing genes in autoimmune diabetes decreases with age, probably due to increasing influence of environmental factors. Autoimmune diabetes with manifestation in adults may have partly different immunogenetic etiopathogenesis than autoimmune diabetes with manifestation in childhood. Compared to fast progressing adult-onset T1DM, slowly progressing adult-onset type 1 diabetes (LADA) might involve genes leading to a slow progressive beta-cells destruction.

摘要

自身免疫性糖尿病,称为1型糖尿病(T1DM),是由胰腺中胰岛β细胞的自身免疫性破坏引起的。通过不同基因组筛查定位的T1DM易感基因座为IDDM1-IDDM18。据估计,HLA(IDDM1)在T1DM的家族聚集性中占比高达40%-50%(对数优势分数为65.8)。许多研究证实,DQB10302是一个强烈的易感基因,并且HLA-DR4单倍型上的DQA10301-DQB10302与HLA-DR3单倍型上的DQA10501-DQB1*0201的杂合组合会导致T1DM风险协同增加。自身免疫性糖尿病中易感基因的存在随年龄增长而减少,这可能是由于环境因素的影响增加所致。与儿童期发病的自身免疫性糖尿病相比,成人期发病的自身免疫性糖尿病可能在免疫遗传病因学上有所不同。与快速进展的成人发病型T1DM相比,缓慢进展的成人发病型1型糖尿病(LADA)可能涉及导致β细胞缓慢破坏的基因。

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