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Protective Effect of the HLA-DRB1*13:02 Allele in Japanese Rheumatoid Arthritis Patients

机译:HLA-DRB1 * 13:02等位基因对日本类风湿关节炎患者的保护作用

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摘要

Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease. Certain HLA-DRB1 “shared-epitope” alleles are reported to be positively associated with increased RA susceptibility, whereas some of the other alleles may be negatively associated. However, studies on the latter are rare. Here, we focus on the protective effects of DRB1 alleles in Japanese RA patients in an association study. Relative predispositional effects (RPE) were analyzed by sequential elimination of carriers of each allele with the strongest association. The protective effects of DRB1 alleles were investigated in patients stratified according to whether they possessed anti-citrullinated peptide antibodies (ACPA). The DRB1*13:02 allele was found to be negatively associated with RA (P = 4.59×10−10, corrected P (Pc) = 1.42×10−8, odds ratio [OR] 0.42, 95% CI 0.32–0.55, P [RPE] = 1.27×10−6); the genotypes DRB1*04:05/*13:02 and *09:01/*13:02 were also negatively associated with RA. The protective effect of *13:02 was also present in ACPA-positive patients (P = 3.95×10−8, Pc = 1.22×10−6, OR 0.42, 95%CI 0.31–0.58) whereas *15:02 was negatively associated only with ACPA-negative RA (P = 8.87×10−5, Pc = 0.0026, OR 0.26, 95%CI 0.12–0.56). Thus, this study identified a negative association of DRB1*13:02 with Japanese RA; our findings support the protective role of DRB1*13:02 in the pathogenesis of ACPA-positive RA.
机译:类风湿关节炎(RA)是一种慢性全身性炎症性疾病。据报道,某些HLA-DRB1“共有表位”等位基因与RA易感性呈正相关,而其他一些等位基因则可能呈负相关。但是,关于后者的研究很少。在这里,我们在一项关联研究中重点研究了DRB1等位基因对日本RA患者的保护作用。通过顺序消除每个等位基因具有最强关联的携带者来分析相对易感作用(RPE)。根据是否具有抗瓜氨酸肽抗体(ACPA)来对分层的患者进行DRB1等位基因的保护作用研究。发现DRB1 * 13:02等位基因与RA呈负相关(P = 4.59×10 -10 ,校正后的P(Pc)= 1.42×10 -8 ,比值比[OR] 0.42,95%CI 0.32–0.55,P [RPE] = 1.27×10 -6 );基因型DRB1 * 04:05 / * 13:02和* 09:01 / * 13:02也与RA呈负相关。 * 13:02的保护作用在ACPA阳性患者中也存在(P = 3.95×10 -8 ,Pc = 1.22×10 -6 ,或0.42, 95%CI 0.31-0.58),而* 15:02仅与ACPA阴性RA呈负相关(P = 8.87×10 -5 P c = 0.0026,OR 0.26,95%CI 0.12-0.56)。因此,本研究发现 DRB1 * 13:02 与日本RA呈负相关;我们的发现支持 DRB1 * 13:02 在ACPA阳性RA发病机理中的保护作用。

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