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A meta-analysis of the role of p38 mitogen-activated protein kinase inhibitors in patients with active rheumatoid arthritis

机译:p38丝裂原活化蛋白激酶抑制剂在活动性类风湿关节炎患者中作用的荟萃分析

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摘要

The role of p38 mitogen-activated protein kinase (MAPK) inhibitors for treating rheumatoid arthritis (RA) is debated. Therefore, we performed a meta-analysis of all published randomized controlled trials (RCTs) to evaluate the efficacy and safety of p38 MAPK inhibitors in patients with active RA. Searches were conducted in the databases PubMed, EMBASE, and Cochrane Library. We identified three articles including four RCTs with analysis on the efficacy and safety of p38 inhibitors for the treatment of RA. Our meta-analysis showed that a better American College of Rheumatology 20 % improvement (ACR20) was observed in the p38 inhibitors group compared with the placebo group, but there were no meaningful differences in ACR50, Disease Activity Score in 28 joints response, and CRP levels between two groups past week 12. The overall adverse events were similar between placebo and treatment groups. In conclusion, p38 MAPK inhibitors showed modest efficacy in patients with RA. However, this conclusion is based on the small number of available studies and inadequate sample size, and more well-designed RCTs will be necessary to determine the role of p38 MAPK inhibitors in RA.
机译:讨论了p38丝裂原活化蛋白激酶(MAPK)抑制剂在治疗类风湿关节炎(RA)中的作用。因此,我们对所有公开的随机对照试验(RCT)进行了荟萃分析,以评估p38 MAPK抑制剂在活动性RA患者中的疗效和安全性。搜索在数据库PubMed,EMBASE和Cochrane库中进行。我们鉴定了三篇文章,包括四篇RCT,并分析了p38抑制剂治疗RA的功效和安全性。我们的荟萃分析显示,与安慰剂组相比,p38抑制剂组观察到美国风湿病学会改善了20%(ACR20),但ACR50、28个关节反应的疾病活动性评分和CRP没有有意义的差异过去12周两组之间的水平相同。安慰剂组和治疗组之间的总体不良事件相似。总之,p38 MAPK抑制剂在RA患者中显示适度的疗效。但是,该结论是基于少量可用研究和样本量不足而得出的,需要更多设计良好的RCT来确定p38 MAPK抑制剂在RA中的作用。

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