Rheumatology, UPMC, Institut Pierre Louis d'épidémiologie et Santé publique, GRC 08, Paris, France.
Department of Rhumatologie, AP-HP, GH Pitié Salpêtrière, Paris, France.
Ann Rheum Dis. 2018 Aug;77(8):1099-1106. doi: 10.1136/annrheumdis-2017-212612. Epub 2018 Jun 8.
Recent advances in knowledge of the pathogenesis of rheumatoid arthritis (RA) has led to promoting very early intervention.
To assess the efficacy of therapeutic interventions in preventing or delaying RA onset with a systematic literature review (SLR) and meta-analysis (MA).
The SLR aimed to include all reports of randomised controlled trials of disease-modifying antirheumatic drugs or glucocorticoids used in patients presenting genetic and/or environmental risk factors for RA and/or systemic autoimmunity associated with RA, and/or symptoms without clinical arthritis and/or unclassified arthritis and in patients with RA. We searched PubMed, EMBASE and Cochrane databases for English articles published from 2006 to 2016 using the keywords 'undifferentiated arthritis' or 'very early rheumatoid arthritis' with 'therapy' or 'treatment'. Main outcome was RA occurrence, defined as fulfilment of the 1987 ACR criteria. The MA was performed with RevMan with the Mantel-Haenszel method.
Among 595 abstracts screened, 10 reports of trials were selected. The studies included 1156 patients, with mean symptom duration 16.2±12.6 weeks. The occurrence of RA was available for nine studies, assessing methylprednisolone, methotrexate, a tumour necrosis factor blocker, abatacept or rituximab. In the group arthralgia without arthritis (people at risk of RA), the MA of the two available studies did not show significant reduction in RA occurrence at week 52 or more (pooled OR 0.74, 95% CI 0.37 to 1.49). For people with undifferentiated arthritis, the MA of the seven available studies revealed significant risk reduction with OR 0.73(95% CI 0.56 to 0.97).
This MA demonstrates that early therapeutic intervention may significantly reduce the risk of RA onset in this very first phase of the disease.
类风湿关节炎(RA)发病机制的研究进展,促使人们开始提倡早期干预。
通过系统文献回顾(SLR)和荟萃分析(MA)评估治疗干预措施预防或延迟 RA 发病的疗效。
SLR 的目标是纳入所有关于疾病修饰抗风湿药物或糖皮质激素治疗的随机对照试验报告,这些药物用于出现 RA 遗传和/或环境危险因素和/或与 RA 相关的系统性自身免疫、以及/或无临床关节炎和/或未分类关节炎和/或 RA 症状的患者。我们使用“未分化关节炎”或“早期类风湿关节炎”和“治疗”或“疗法”等关键词,在 PubMed、EMBASE 和 Cochrane 数据库中搜索了 2006 年至 2016 年发表的英文文章。主要结局是 RA 发病,定义为符合 1987 年 ACR 标准。MA 采用 RevMan 软件,使用 Mantel-Haenszel 法进行分析。
在筛选的 595 篇摘要中,有 10 项试验报告入选。这些研究共纳入 1156 例患者,平均症状持续时间为 16.2±12.6 周。9 项研究报告了 RA 发病情况,评估了甲泼尼龙、甲氨蝶呤、肿瘤坏死因子阻滞剂、阿巴西普或利妥昔单抗的疗效。在关节炎前期(有 RA 发病风险的人群),两项可用研究的 MA 结果显示,在第 52 周或更长时间内,RA 发病的风险没有显著降低(合并 OR 0.74,95%CI 0.37 至 1.49)。对于未分化关节炎患者,7 项可用研究的 MA 显示,早期治疗可显著降低 RA 发病风险,OR 为 0.73(95%CI 0.56 至 0.97)。
本 MA 表明,在疾病的最初阶段,早期治疗干预可能显著降低 RA 发病风险。