Kim Seong-Kyu, Choe Jung-Yoon, Bae Jisuk, Chae Soo-Cheon, Park Dong-Jin, Kwak Sang Gyu, Lee Shin-Seok
Rheumatology (Oxford). 2014 Jun;53(6):1009-13. doi: 10.1093/rheumatology/ket473.
We investigated the relationship between polymorphisms in the TNF-a-induced protein 3 (TNFAIP3) gene and genetic susceptibility to SLE and RA in the Korean population.
The present case control study included 422 patients with RA, 133 patients with SLE and 422 healthy controls. Genotyping for TNFAIP3 gene polymorphisms rs5029941 (C>T), rs2230926 (T>G), rs5029930 (C>A), rs5029937 (G>T) and rs5029939 (G>C) in TNFAIP3 gene polymorphisms was performed. The status of RA-related autoantibodies, including RF and anti-CCP, in RA and the presence of arthritis and nephritis in SLE were assessed.
Significantly different frequencies of minor alleles in two TNFAIP3 polymorphisms were found in patients with SLE compared with healthy controls [odds ratio (OR) 2.13, 95% CI 1.25, 3.65, P= 0.02 for rs5029937; OR 2.17, 95% CI 1.27, 3.72, P= 0.01 for rs5029939). Moreover, patients with SLE showed different frequencies of haplotypes compared with healthy controls (P<0.001). However, no association was found between RA susceptibility and TNFAIP3 polymorphisms (P= 0.28). Interactions between RA-related autoantibody status and TNFAIP3 polymorphisms were not associated with RA susceptibility. Interestingly, arthritis in patients with SLE was marginally associated with TNFAIP3 polymorphisms (P= 0.04).
The results suggest that TNFAIP3 gene polymorphisms are associated with differential susceptibility to SLE and RA in the Korean population. The relationship between TNFAIP3 gene polymorphisms and RA susceptibility may be dependent on ethnic background.
我们研究了韩国人群中肿瘤坏死因子-α诱导蛋白3(TNFAIP3)基因多态性与系统性红斑狼疮(SLE)和类风湿关节炎(RA)遗传易感性之间的关系。
本病例对照研究纳入了422例RA患者、133例SLE患者和422名健康对照。对TNFAIP3基因多态性rs5029941(C>T)、rs2230926(T>G)、rs5029930(C>A)、rs5029937(G>T)和rs5029939(G>C)进行基因分型。评估了RA患者中类风湿因子(RF)和抗环瓜氨酸肽(anti-CCP)等RA相关自身抗体的状态,以及SLE患者中关节炎和肾炎的存在情况。
与健康对照相比,SLE患者中两个TNFAIP3多态性的次要等位基因频率存在显著差异[rs5029937的比值比(OR)为2.13,95%置信区间(CI)为1.25至3.65,P=0.02;rs5029939的OR为2.17,95%CI为1.27至3.72,P=0.01]。此外,与健康对照相比,SLE患者的单倍型频率也有所不同(P<0.001)。然而,未发现RA易感性与TNFAIP3多态性之间存在关联(P=0.28)。RA相关自身抗体状态与TNFAIP3多态性之间的相互作用与RA易感性无关。有趣的是,SLE患者的关节炎与TNFAIP3多态性存在微弱关联(P=0.04)。
结果表明,TNFAIP3基因多态性与韩国人群中SLE和RA的易感性差异有关。TNFAIP3基因多态性与RA易感性之间的关系可能取决于种族背景。