Lee Young Ho, Ji Jong Dae, Song Gwan Gyu
Division of Rheumatology, Department of Internal Medicine, Korea University Medical Center, Korea University, College of Medicine, Seoul, Korea.
J Rheumatol. 2008 Nov;35(11):2129-35. doi: 10.3899/jrheum.080186. Epub 2008 Oct 1.
.To investigate whether the Fcgamma receptor (FCGR) polymorphism confers susceptibility to rheumatoid arthritis (RA).
We conducted metaanalyses on the associations between FCGR polymorphisms and RA susceptibility as determined using (1) allele contrast, (2) recessive models, (3) dominant models, and (4) contrast of homozygotes, using fixed or random effects models.
A total of 10 separate comparisons were considered, which comprised 6 European and 4 Asian population samples. Metaanalysis of FCGR3A polymorphism revealed a significant association between the VV genotype and the risk of developing RA relative to the VF+FF genotype (OR 1.256, 95% CI 1.045-1.510, p = 0.015), with no evidence of between-study heterogeneity (p = 0.167). In subjects of European descent, a stronger association was observed between the VV genotype and RA than for the FF genotype (OR 1.374, 95% CI 1.101-1.714, p = 0.005). In Asians, no such association was found. Metaanalysis of the VV vs FF genotype revealed a significantly increased OR in Europeans (OR 1.399, 95% CI 1.107-1.769, p = 0.005), but not in Asians. No association was found between RA and the FCGR2A and FCGR3B polymorphisms in all subjects and in European and Asian populations, except for the NA22 vs NA11 of FCGR3B in Europeans.
No relation was found between the FCGR2A polymorphism and susceptibility to RA in Europeans or Asians. The FCGR3A polymorphism was found to be associated with RA in Europeans but not in Asians. The FCGR3B polymorphism was associated with RA susceptibility in Europeans.
研究Fcγ受体(FCGR)基因多态性是否与类风湿关节炎(RA)易感性相关。
我们采用固定效应模型或随机效应模型,对FCGR基因多态性与RA易感性之间的关联进行了荟萃分析,分析方法包括:(1)等位基因对比;(2)隐性模型;(3)显性模型;(4)纯合子对比。
共纳入10项独立比较,包括6个欧洲人群样本和4个亚洲人群样本。FCGR3A基因多态性的荟萃分析显示,与VF + FF基因型相比,VV基因型与发生RA的风险显著相关(比值比[OR] 1.256,95%置信区间[CI] 1.045 - 1.510,p = 0.015),且无研究间异质性证据(p = 0.167)。在欧洲血统受试者中,观察到VV基因型与RA的关联比FF基因型更强(OR 1.374,95% CI 1.101 - 1.714,p = 0.005)。在亚洲人中未发现此类关联。VV与FF基因型的荟萃分析显示,欧洲人OR显著升高(OR 1.399,95% CI 1.107 - 1.769,p = 0.005),但亚洲人未升高。在所有受试者以及欧洲和亚洲人群中,除欧洲人中FCGR3B的NA22与NA11外,未发现RA与FCGR2A和FCGR3B基因多态性之间存在关联。
在欧洲人或亚洲人中,未发现FCGR2A基因多态性与RA易感性之间存在关联。发现FCGR3A基因多态性在欧洲人与RA相关,但在亚洲人中无此关联。FCGR3B基因多态性与欧洲人的RA易感性相关。