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

被引:87
作者
Broen, Jasper C. A. [1 ]
Radstake, Timothy R. D. J. [1 ]
Rossato, Marzia [1 ]
机构
[1] Univ Med Ctr Utrecht, Lab Translat Immunol, Dept Rheumatol & Clin Immunol, NL-3584 CX Utrecht, Netherlands
关键词
GENOME-WIDE ASSOCIATION; I COLLAGEN EXPRESSION; GROWTH-FACTOR-BETA; CD4+ T-CELLS; TGF-BETA; DOWN-REGULATION; RISK-FACTOR; LUPUS-ERYTHEMATOSUS; FUNCTIONAL VARIANTS; AUTOIMMUNE-DISEASE;
D O I
10.1038/nrrheum.2014.128
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
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.
引用
收藏
页码:671 / 681
页数:11
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