医学
阿巴塔克普
托珠单抗
类风湿性关节炎
内科学
痹症科
关节炎
肿瘤坏死因子抑制剂
类风湿因子
耐火材料(行星科学)
阿达木单抗
肿瘤坏死因子α
依那西普
美罗华
物理
淋巴瘤
天体生物学
作者
Yuichi Yamasaki,Akihiro Nakamura,Tomohiro Kubota,Takuro Mitsunobu,Mizuki Moriyama,Syuji Takei,Yasuhiro Okamoto
摘要
Currently, no indicators on which biologic disease-modifying anti-rheumatic drugs (bDMARDs) should be used first for juvenile idiopathic arthritis (JIA) have been established. Thus, this study aimed to determine the useful biomarkers in JIA to enable the best selection of the first bDMARDs without primary failure.This retrospective study used data of patients examined for JIA between 2015 and 2021 at Kagoshima University Hospital in Japan.Altogether, 67 cases of non-systemic JIA were analyzed, excluding cases that had been treated for <6 months. Of the 67 cases, 52 were treated with bDMARDs and all rheumatoid factor (RF)+ types (32 cases) were treated with bDMARDs. Eleven cases (31.4&) (all were RF+ types and used anti-tumor necrosis factor (TNF)α agents) switched to other bDMARDs because of primary failure, and nine cases had secondary failure (6;anti-TNF, 3;anti-Interleukin-6). A significant difference in pre-treatment RF values (177.9 vs 25.7 IU/ml, p = 0.002) and presence (Odds Ratio 1.952,p = 0.004) were observed between the primary failure group and effective group.RF+ JIA required bDMARDs with high probability. JIA with high titre of RF tends to be refractory to anti-TNFα agents. Tocilizumab or abatacept could be a first-choice bDMARD in such cases.
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