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Arthritis Rheum. 2012 Sep;64(9):2824-35. doi: 10.1002/art.34498.
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2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis.2008年美国风湿病学会关于使用改善病情抗风湿药和生物制剂治疗类风湿关节炎的建议的2012年更新版。
Arthritis Care Res (Hoboken). 2012 May;64(5):625-39. doi: 10.1002/acr.21641.
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Combination etanercept and methotrexate provides better disease control in very early (<=4 months) versus early rheumatoid arthritis (>4 months and <2 years): post hoc analyses from the COMET study.联合依那西普和甲氨蝶呤在非常早期(<=4 个月)与早期类风湿关节炎(>4 个月且<2 年)相比能更好地控制疾病:来自 COMET 研究的事后分析。
Ann Rheum Dis. 2012 Jun;71(6):989-92. doi: 10.1136/annrheumdis-2011-201066. Epub 2012 Mar 8.
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The need to better classify and diagnose early and very early rheumatoid arthritis.需要更好地对早期和极早期类风湿关节炎进行分类和诊断。
J Rheumatol. 2012 Feb;39(2):212-7. doi: 10.3899/jrheum.110967. Epub 2011 Dec 15.
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In early rheumatoid arthritis, patients with a good initial response to methotrexate have excellent 2-year clinical outcomes, but radiological progression is not fully prevented: data from the methotrexate responders population in the SWEFOT trial.在早期类风湿关节炎中,对甲氨蝶呤初始反应良好的患者具有极佳的 2 年临床结局,但并不能完全预防影像学进展:来自 SWEFOT 试验中甲氨蝶呤应答者人群的数据。
Ann Rheum Dis. 2012 Feb;71(2):186-91. doi: 10.1136/annrheumdis-2011-200038. Epub 2011 Sep 19.
6
Delays in assessment of patients with rheumatoid arthritis: variations across Europe.类风湿关节炎患者评估延迟:欧洲各地的差异。
Ann Rheum Dis. 2011 Oct;70(10):1822-5. doi: 10.1136/ard.2011.151902. Epub 2011 Aug 7.
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Inflammatory memories: is epigenetics the missing link to persistent stromal cell activation in rheumatoid arthritis?炎症记忆:表观遗传学是否是类风湿关节炎中基质细胞持续活化的缺失环节?
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The value of early intervention in RA--a window of opportunity.类风湿关节炎早期干预的价值——一个机会之窗。
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Performance of the 2010 ACR/EULAR criteria for rheumatoid arthritis: comparison with 1987 ACR criteria in a very early synovitis cohort.2010 年 ACR/EULAR 类风湿关节炎分类标准的表现:与早期滑膜炎症队列中 1987 年 ACR 标准的比较。
Ann Rheum Dis. 2011 Jun;70(6):949-55. doi: 10.1136/ard.2010.143560. Epub 2011 Feb 1.
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Predictors of response to methotrexate in early DMARD naive rheumatoid arthritis: results from the initial open-label phase of the SWEFOT trial.早期甲氨蝶呤初治类风湿关节炎患者对甲氨蝶呤应答的预测因素:来自 SWEFOT 试验初始开放性标签阶段的结果。
Ann Rheum Dis. 2011 Mar;70(3):469-75. doi: 10.1136/ard.2010.139212. Epub 2010 Dec 13.

早期类风湿关节炎的治疗策略与类风湿关节炎的预防。

Treatment strategies in early rheumatoid arthritis and prevention of rheumatoid arthritis.

机构信息

Division of Rheumatology, University of Colorado School of Medicine, 1775 Aurora Court, Mail Stop B-115, Aurora, CO 80045, USA.

出版信息

Curr Rheumatol Rep. 2012 Oct;14(5):472-80. doi: 10.1007/s11926-012-0275-1.

DOI:10.1007/s11926-012-0275-1
PMID:22773387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3616381/
Abstract

Data now suggest that current strategies in the treatment of rheumatoid arthritis (RA) should focus on early identification and diagnosis, followed by early initiation of DMARD therapy. Initiation of treatment in early RA-ideally, less than 3-6 months after symptom onset-improves the success of achieving disease remission and reduces joint damage and disability. While the optimal treatment regimen in early RA is unclear, use of initial DMARD mono- or combination therapy with prompt escalation to achieve low disease activity or remission is an appropriate approach. Ultimately, the goal of RA management should be the prevention of inflammatory joint disease and, thereby, prevention of disability. To date, studies have shown that pharmacologic interventions can delay progression from undifferentiated inflammatory arthritis to classifiable RA. However, further investigation is needed to identify asymptomatic individuals at high risk for future RA and to intervene early enough in the pathogenesis of RA to prevent progression to clinical disease.

摘要

目前的数据表明,类风湿关节炎(RA)的治疗策略应侧重于早期识别和诊断,然后尽早开始 DMARD 治疗。在早期 RA 中开始治疗(理想情况下,症状出现后 3-6 个月内)可提高实现疾病缓解的成功率,并减少关节损伤和残疾。虽然早期 RA 的最佳治疗方案尚不清楚,但初始 DMARD 单药或联合治疗并迅速升级以实现低疾病活动度或缓解是一种合适的方法。最终,RA 管理的目标应该是预防炎症性关节疾病,从而预防残疾。迄今为止,研究表明,药物干预可以延缓未分化炎症性关节炎向可分类 RA 的进展。然而,需要进一步研究以确定未来患 RA 风险高的无症状个体,并在 RA 的发病机制中尽早干预,以防止疾病进展至临床疾病。