Korman B D, Alba M I, Le J M, Alevizos I, Smith J A, Nikolov N P, Kastner D L, Remmers E F, Illei G G
Complex Disease Genetics Unit, Genetics and Genomics Branch, National Institute of Arthritis, Musculoskeletal, and Skin Diseases, Bethesda, MD 20892, USA.
Genes Immun. 2008 Apr;9(3):267-70. doi: 10.1038/gene.2008.1. Epub 2008 Feb 14.
Single nucleotide polymorphisms in the STAT4 gene have recently been shown to be associated with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). Primary Sjögren's syndrome (pSS) is a related autoimmune disease thought to have a pathogenesis similar to these diseases. To test the hypothesis that the variant haplotype of STAT4 seen in RA and SLE is also associated with pSS, we genotyped rs7574865, the most strongly disease-associated SNP in the variant STAT4 haplotype, in 124 Caucasian pSS subjects and compared them to 1143 Caucasian controls. The disease-associated T allele was more common in chromosomes of the pSS patients (29.6%) than in controls (22.3%), leading to a P-value for association of 0.01. These results implicate polymorphisms in the STAT4 gene in the pathogenesis of pSS.
信号转导和转录激活因子4(STAT4)基因中的单核苷酸多态性最近已被证明与类风湿性关节炎(RA)和系统性红斑狼疮(SLE)有关。原发性干燥综合征(pSS)是一种相关的自身免疫性疾病,其发病机制被认为与这些疾病相似。为了检验在RA和SLE中发现的STAT4变异单倍型也与pSS相关的假设,我们对124名白种人pSS患者的rs7574865进行了基因分型,rs7574865是变异STAT4单倍型中与疾病关联最强的单核苷酸多态性,并将他们与1143名白种人对照进行比较。与疾病相关的T等位基因在pSS患者的染色体中(29.6%)比在对照中(22.3%)更常见,导致关联的P值为0.01。这些结果表明STAT4基因多态性参与了pSS的发病机制。