Terao Chikashi, Ohmura Koichiro, Kawaguchi Yasushi, Nishimoto Tetsuya, Kawasaki Aya, Takehara Kazuhiko, Furukawa Hiroshi, Kochi Yuta, Ota Yuko, Ikari Katsunori, Sato Shinichi, Tohma Shigeto, Yamada Ryo, Yamamoto Kazuhiko, Kubo Michiaki, Yamanaka Hisashi, Kuwana Masataka, Tsuchiya Naoyuki, Matsuda Fumihiko, Mimori Tsuneyo
Kyoto University, Kyoto, Japan.
Arthritis Rheum. 2013 Feb;65(2):472-80. doi: 10.1002/art.37777.
Systemic sclerosis (SSc) is an autoimmune disease for which multiple susceptibility genes have been reported. Genome-wide association studies have shown that large numbers of susceptibility genes are shared among autoimmune diseases. Recently, our group identified 9 novel susceptibility genes associated with rheumatoid arthritis (RA) in a Japanese population. The aim of this study was to elucidate whether the 18 genes that displayed associations or suggestive associations for RA in our previous study are associated with SSc in Japanese.
We performed an association study that included 415 patients with SSc and 16,891 control subjects, followed by a replication study that included 315 patients and 21,054 control subjects. The 18 markers reported to display association with RA were analyzed for their associations with SSc in the first study, and 5 markers were further analyzed in the replication study. The inverse variance method was used to evaluate the associations of these markers with SSc in a combined study.
In the phospholipase D4 gene (PLD4), rs2841277 displayed a significant association with SSc in Japanese patients (P = 0.00017). We observed that rs2841280 in exon 2 of PLD4 was in strong linkage disequilibrium with rs2841277 and introduced an amino acid alteration. We also observed associations between SSc and rs6932056 in TNFAIP3 and rs2280381 in IRF8 (P = 0.0000095 and P = 0.0030, respectively), both of which displayed associations with SSc in a European population.
We determined that PLD4 is a novel susceptibility gene for SSc in Japanese, thus confirming the involvement of PLD4 in autoimmunity. Associations between SSc and TNFAIP3 or IRF8 were also detected in our Japanese population. SSc and RA appear to share relatively large proportions of their genetic backgrounds.
系统性硬化症(SSc)是一种已报道有多个易感基因的自身免疫性疾病。全基因组关联研究表明,大量易感基因在自身免疫性疾病中是共享的。最近,我们小组在日本人群中鉴定出9个与类风湿关节炎(RA)相关的新易感基因。本研究的目的是阐明在我们之前的研究中显示与RA有关联或提示性关联的18个基因是否与日本人群中的SSc相关。
我们进行了一项关联研究,纳入了415例SSc患者和16891例对照受试者,随后进行了一项重复研究,纳入了315例患者和21054例对照受试者。在第一项研究中分析了报道与RA有关联的18个标记与SSc的关联,在重复研究中进一步分析了5个标记。在一项合并研究中使用逆方差法评估这些标记与SSc的关联。
在磷脂酶D4基因(PLD4)中,rs2841277与日本患者的SSc显示出显著关联(P = 0.00017)。我们观察到PLD4外显子2中的rs2841280与rs284,1277处于强连锁不平衡状态,并导致了氨基酸改变。我们还观察到SSc与TNFAIP3中的rs6932056和IRF8中的rs2280381之间存在关联(分别为P =,0000095和P = 0.0030),这两个标记在欧洲人群中均与SSc显示出关联。
我们确定PLD4是日本人群中SSc的一个新易感基因,从而证实了PLD4参与自身免疫。在我们的日本人群中也检测到了SSc与TNFAIP3或IRF8之间的关联。SSc和RA似乎共享相对较大比例的遗传背景。