Division of Rheumatology, University of Colorado School of Medicine, Aurora, CO, USA.
Best Pract Res Clin Rheumatol. 2013 Aug;27(4):467-85. doi: 10.1016/j.berh.2013.09.002. Epub 2013 Oct 2.
The discovery of elevations of rheumatoid arthritis (RA)-related biomarkers prior to the onset of clinically apparent RA raises hopes that individuals who are at risk of future RA can be identified in a preclinical phase of disease that is defined as abnormalities of RA-related immune activity prior to the clinically apparent onset of joint disease. Additionally, there is a growing understanding of the immunologic processes that are occurring in preclinical RA, as well as a growing understanding of risk factors that may be mechanistically related to RA development. Furthermore, there are data supporting that treatment of early RA can lead to drug-free remission. Taken as a whole, these findings suggest that it may be possible to use biomarkers and other factors to accurately identify the likelihood and timing of onset of future RA, and then intervene with immunomodulatory therapies and/or risk factor modification to prevent the future onset of RA in at-risk individuals. Importantly, several clinical prevention trials for RA have already been tried, and one is underway. However, while our growing understanding of the mechanisms and natural history of RA development may be leading us to the implementation of prevention strategies for RA, there are still several challenges to be met. These include developing sufficiently accurate methods of predicting those at high risk of future RA so that clinical trials can be developed based on accurate rates of development of arthritis and subjects can be adequately informed of their risk of disease, identifying the appropriate interventions and biologic targets for optimal prevention, and addressing the psychosocial and economic aspects that are crucial to developing broadly applicable prevention measures for RA. These issues notwithstanding, prevention of RA may be within reach in the near future.
类风湿关节炎(RA)相关生物标志物在临床明显 RA 发病前升高的发现,使人们希望能够在疾病的临床前阶段,即关节疾病临床明显发作前的 RA 相关免疫活性异常阶段,识别出未来有患 RA 风险的个体。此外,人们对临床前 RA 中发生的免疫过程有了更多的了解,对可能与 RA 发展机制相关的危险因素也有了更多的了解。此外,有数据支持早期 RA 的治疗可以导致无药物缓解。综上所述,这些发现表明,有可能使用生物标志物和其他因素来准确识别未来 RA 的发病可能性和时间,并通过免疫调节治疗和/或危险因素修改来预防高危个体未来发生 RA。重要的是,已经尝试了几项针对 RA 的临床预防试验,其中一项正在进行中。然而,尽管我们对 RA 发病机制和自然史的认识不断加深,可能会促使我们实施 RA 预防策略,但仍有几个挑战需要应对。这些包括开发出足够准确的方法来预测那些未来患 RA 风险较高的人,以便能够根据关节炎的发展速度开发临床试验,并让受试者充分了解他们的患病风险,确定最佳预防的适当干预措施和生物靶点,以及解决对开发广泛适用的 RA 预防措施至关重要的社会心理和经济方面的问题。尽管存在这些问题,但在不久的将来,预防 RA 可能即将实现。