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The role of genetics and epigenetics in the pathogenesis of systemic sclerosis

机译:遗传学和表观遗传学在系统性硬化症发病机制中的作用

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摘要

Systemic sclerosis (SSc) is a complex autoimmune disease of unclear aetiology. A multitude of genetic studies, ranging from candidate-gene studies to genome-wide association studies, have identified a large number of genetic susceptibility factors for SSc and its clinical phenotypes, but the contribution of these factors to disease susceptibility is only modest. However, in an endeavour to explore how the environment might affect genetic susceptibility, epigenetic research into SSc is rapidly expanding. Orchestrated by environmental factors, epigenetic modifications can drive genetically predisposed individuals to develop autoimmunity, and are thought to represent the crossroads between the environment and genetics in SSc. Therefore, in addition to providing a comprehensive description of the current understanding of genetic susceptibility underlying SSc, this Review describes the involvement of epigenetic phenomena, including DNA methylation patterns, histone modifications and microRNAs, in SSc.
机译:系统性硬化症(SSc)是一种病因不明的复杂自身免疫性疾病。从候选基因研究到全基因组关联研究,许多遗传学研究已经确定了SSc及其临床表型的大量遗传易感性因素,但是这些因素对疾病易感性的贡献仅是适度的。然而,为了探索环境如何影响遗传易感性,对SSc的表观遗传学研究正在迅速扩展。受环境因素影响,表观遗传修饰可以驱动遗传易感个体发展自身免疫性,并被认为代表了SSc中环境与遗传学之间的交叉路口。因此,除了全面介绍SSc的遗传易感性的当前理解外,本综述还描述了SSc中涉及表观遗传现象,包括DNA甲基化模式,组蛋白修饰和microRNA。

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