Kastbom Alf, Bratt Johan, Ernestam Sofia, Lampa Jon, Padyukov Leonid, Söderkvist Peter, Skogh Thomas
Linköping University, Linköping, Sweden.
Arthritis Rheum. 2007 Feb;56(2):448-52. doi: 10.1002/art.22390.
To determine whether a functional single-nucleotide polymorphism in the gene encoding Fcgamma receptor type IIIA (FcgammaRIIIA) correlates with the response to treatment with tumor necrosis factor alpha inhibitors in rheumatoid arthritis (RA).
The study population comprised 282 Swedish patients with RA in whom the therapeutic efficacy of conventional disease-modifying antirheumatic drugs had been insufficient. Infliximab or etanercept treatment was initiated, and patients were evaluated after 3 months, using the American College of Rheumatology 20% improvement criteria (ACR20), the ACR50, and the ACR70 or the European League Against Rheumatism (EULAR) criteria. The chi-square test was used to compare response rates across FcgammaRIIIA genotypes.
No differences in genotype distribution were observed among nonresponders compared with ACR20 responders (P = 0.80), ACR50 responders (P = 0.56), or ACR70 responders (P = 0.91). Similar results were observed when analyzing infliximab and etanercept separately or when using the EULAR response criteria.
Unlike the findings of a previous study, the results of the current study suggest that the 158V/F polymorphism of FcgammaRIIIA is very unlikely to influence the clinical efficacy of infliximab or etanercept in patients with RA.
确定编码ⅢA型Fcγ受体(FcγRIIIA)基因中的功能性单核苷酸多态性是否与类风湿关节炎(RA)患者对肿瘤坏死因子α抑制剂治疗的反应相关。
研究人群包括282名瑞典RA患者,这些患者使用传统抗风湿药物治疗效果不佳。开始使用英夫利昔单抗或依那西普治疗,3个月后根据美国风湿病学会20%改善标准(ACR20)、ACR50和ACR70或欧洲抗风湿病联盟(EULAR)标准对患者进行评估。采用卡方检验比较不同FcγRIIIA基因型的反应率。
无反应者与达到ACR20反应者(P = 0.80)、ACR50反应者(P = 0.56)或ACR70反应者(P = 0.91)相比,基因型分布无差异。分别分析英夫利昔单抗和依那西普或使用EULAR反应标准时,观察到类似结果。
与之前一项研究的结果不同,本研究结果表明,FcγRIIIA的158V/F多态性极不可能影响英夫利昔单抗或依那西普对RA患者的临床疗效。