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Genetic aspects of type 1 diabetes

机译:1型糖尿病的遗传因素

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摘要

Type 1 diabetes mellitus (T1DM) is characterized by autoimmune destruction of pancreatic beta-cells in genetically predisposed individuals, eventually resulting in severe insulin deficiency. It is the most common form of diabetes in children and adolescents. Genetic susceptibility plays a crucial role in development of T1DM. The human leukocyte antigen complex plays a key role in the pathogenesis of T1DM. Furthermore, genome-wide association studies and linkage analysis have recently made a significant contribution to current knowledge relative to the impact of genetics on T1DM development and progression. This review focuses on current knowledge of genetics as a pathogenesis for T1DM. It also discusses mechanisms by which genes influence the risk of developing T1DM as well as the clinical and research applications of genetic risk scores in T1DM.
机译:1型糖尿病(T1DM)的特征是遗传易感人群中胰腺β细胞的自身免疫破坏,最终导致严重的胰岛素缺乏。它是儿童和青少年中最常见的糖尿病形式。遗传易感性在T1DM的发展中起着至关重要的作用。人白细胞抗原复合物在T1DM的发病机理中起关键作用。此外,全基因组关联研究和连锁分析最近对有关遗传对T1DM发育和进展的影响的当前知识做出了重要贡献。这篇综述侧重于遗传学作为T1DM发病机理的当前知识。它还讨论了基因影响T1DM风险的机制,以及T1DM中遗传风险评分的临床和研究应用。

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