Kobayashi Shu, Ikari Katsunori, Kaneko Hirotaka, Kochi Yuta, Yamamoto Kazuhiko, Shimane Kenichi, Nakamura Yusuke, Toyama Yoshiaki, Mochizuki Takeshi, Tsukahara So, Kawaguchi Yasushi, Terai Chihiro, Hara Masako, Tomatsu Taisuke, Yamanaka Hisashi, Horiuchi Takahiko, Tao Kayoko, Yasutomo Koji, Hamada Daisuke, Yasui Natsuo, Inoue Hiroshi, Itakura Mitsuo, Okamoto Hiroshi, Kamatani Naoyuki, Momohara Shigeki
Tokyo Women's Medical University, Tokyo, Japan.
Arthritis Rheum. 2008 Jul;58(7):1940-6. doi: 10.1002/art.23494.
STAT4 encodes a transcriptional factor that transmits signals induced by several key cytokines, and it might be a key molecule in the development of autoimmune diseases. Recently, a STAT4 haplotype was reported to be associated with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) in Caucasian populations. This was replicated in a Korean RA population. Interestingly, the degree of risk of RA susceptibility with the STAT4 haplotype was similar in the Caucasian and Korean populations. The present study was undertaken to investigate the effect of STAT4 on susceptibility to RA and SLE in the Japanese.
We performed an association study using 3 independent Japanese RA case-control populations (total 3,567 cases and 2,199 controls) and 3 independent Japanese SLE populations (total 591 cases). All samples were genotyped using the TaqMan fluorogenic 5' nuclease assay for single-nucleotide polymorphism (SNP) rs7574865, which tags the susceptibility haplotype. The association of the SNP with disease susceptibility in each case-control study was calculated using Fisher's exact test, and the results were combined, using the Mantel-Haenszel method, to obtain combined odds ratios (ORs).
We observed a significant association of the STAT4 polymorphism with susceptibility to both RA and SLE. The combined ORs for RA and SLE, respectively, were 1.27 (P = 8.4 x 10(-9)) and 1.61 (P = 2.1 x 10(-11)) for allele frequency distribution; these ORs were quite similar to those previously observed in the Caucasian population.
We conclude that STAT4 is associated with RA and SLE in the Japanese. Our results indicate that STAT4 is a common genetic risk factor for autoimmune diseases, with similar strength across major racial groups.
信号转导和转录激活因子4(STAT4)编码一种转录因子,可传递由多种关键细胞因子诱导产生的信号,它可能是自身免疫性疾病发展过程中的关键分子。最近,有报道称一种STAT4单倍型与白种人群的类风湿关节炎(RA)和系统性红斑狼疮(SLE)相关。这一结果在韩国RA人群中得到了重复验证。有趣的是,携带STAT4单倍型的RA易感性风险程度在白种人和韩国人群中相似。本研究旨在调查STAT4对日本人患RA和SLE易感性的影响。
我们使用3个独立的日本RA病例对照人群(共3567例病例和2199例对照)以及3个独立的日本SLE人群(共591例病例)进行了一项关联研究。所有样本均采用TaqMan荧光5'核酸酶分析法对单核苷酸多态性(SNP)rs7574865进行基因分型,该SNP标记了易感单倍型。在每项病例对照研究中,使用Fisher精确检验计算该SNP与疾病易感性的关联,并采用Mantel-Haenszel方法合并结果,以获得合并优势比(OR)。
我们观察到STAT4多态性与RA和SLE的易感性均存在显著关联。对于等位基因频率分布,RA和SLE的合并OR分别为1.27(P = 8.4×10⁻⁹)和1.61(P = 2.1×10⁻¹¹);这些OR与之前在白种人群中观察到的结果非常相似。
我们得出结论,STAT4与日本人的RA和SLE相关。我们的结果表明,STAT4是自身免疫性疾病的一个常见遗传风险因素,在主要种族群体中的作用强度相似。