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类风湿关节炎的风险评估:从基础到临床。

Risk estimation in rheumatoid arthritis: from bench to bedside.

机构信息

Department of Rheumatology, Leiden University Medical Centre, P. O. Box 9600, 2300 RC Leiden, Netherlands.

出版信息

Nat Rev Rheumatol. 2014 Mar;10(3):171-80. doi: 10.1038/nrrheum.2013.215. Epub 2014 Jan 28.

Abstract

The prognosis for patients with rheumatoid arthritis (RA) who were diagnosed in the years since 2010 is much better than for individuals who were diagnosed with the disease 20 years ago. This improvement in the long-term outcome of disease is the result of earlier initiation of therapy, disease-activity-guided modification of treatment and the availability of new, and effective, drugs. Nonetheless, current treatment strategies remain population-based, rather than individualized. Decision-making processes relevant to the provision of individualized treatment require appropriate prognostication with regard to a number of variables. Here, the methods available to evaluate the performance of predictive models are discussed. In addition, I highlight the advances in risk estimation that have been made concerning three treatment decisions relevant to the management of RA that are made daily in the clinic: when to initiate treatment with DMARDs in patients in the early stages of arthritis; the ideal intensity of initial treatment; and the likely responsiveness of the patient to a particular therapy. Apart from a model predicting the development of RA, the majority of prognostic tools derived in arthritis and RA are not accurate or not validated. Hence, personalized treatment decisions in arthritis and RA are still far from bedside.

摘要

对于 2010 年后被诊断为类风湿关节炎 (RA) 的患者,其预后明显好于 20 年前被诊断为该病的患者。疾病长期预后的这种改善是由于更早地开始治疗、根据疾病活动度调整治疗以及新的有效药物的出现。尽管如此,目前的治疗策略仍然基于人群,而不是个体化。与提供个体化治疗相关的决策过程需要对多个变量进行适当的预测。本文讨论了评估预测模型性能的方法。此外,我还强调了在与 RA 管理相关的三个日常临床治疗决策中,风险评估方面的进展:在关节炎早期阶段,何时开始使用 DMARDs 治疗;初始治疗的理想强度;以及患者对特定治疗的可能反应性。除了预测 RA 发展的模型外,大多数源自关节炎和 RA 的预后工具要么不准确,要么未经验证。因此,关节炎和 RA 的个体化治疗决策仍远远不能付诸临床实践。

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