The genetics of scleroderma (systemic sclerosis)

被引:47
作者
Agarwal, Sandeep K. [1 ]
Reveille, John D. [1 ]
机构
[1] Univ Texas Houston, Hlth Sci Ctr, Div Rheumatol & Clin Immunogenet, Dept Internal Med, Houston, TX 77030 USA
关键词
genetics; polymorphisms; scleroderma; systemic sclerosis; SINGLE-NUCLEOTIDE POLYMORPHISM; GENOME-WIDE ASSOCIATION; PERIPHERAL-BLOOD CELLS; FACTOR T-BET; LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS; FUNCTIONAL POLYMORPHISM; TRANSCRIPTION FACTOR; CONFERS SUSCEPTIBILITY; JAPANESE POPULATION;
D O I
10.1097/BOR.0b013e3283367c17
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review To determine the advances made in the genetics of scleroderma in candidate gene association studies. Recent findings Over the past 18 months, a number of candidate gene studies using large case-control.. series in scleroderma have been reported. The studies have identified multiple genes involved in immune regulation including BANK1, C8orf13-BLK, IL-23R, IRF5, STAT4, TBX21, and TNFSF4 as susceptibility genes for the development of SSc. Furthermore, gene-gene interaction studies suggest that IRF5, STAT4, and BANK1 as well as TBX21 and STAT4 interact with regard to scleroderma susceptibility. Many of the genetic variants associated with SSc susceptibility are shared among other autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. Summary Candidate gene association studies have substantially advanced our understanding of the pathogenesis of SSc and demonstrate that SSc is a polygenic, autoimmune disease.
引用
收藏
页码:133 / 138
页数:6
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