Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University and Section of Rheumatology, VA Portland Health Care System, Portland, OR, 97239, USA.
Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University and Section of Rheumatology, VA Portland Health Care System, Portland, OR, 97239, USA.
Best Pract Res Clin Rheumatol. 2022 Mar;36(1):101741. doi: 10.1016/j.berh.2021.101741. Epub 2022 Jan 19.
Highly efficacious drugs are widely available for treating rheumatoid arthritis (RA). However, accurately selecting a likely effective drug for individual RA patients has been challenging. Biomarkers are required since clinical phenotypes are not reliable to guide the choice of drugs. Previously identified genetic variants for predicting treatment response have failed in replication in independent cohorts of RA patients. Recent studies aimed at the discovery of biomarkers to predict treatment response have focused on integrative omics analysis, expanded to the microbiome, and further finer definition of synovial pathotypes. Treatment responders and non-responders of RA patients can be distinguished by distinct signatures at baseline in their gut microbiota compositions, peripheral blood transcriptome profiling or histomorphological and molecular pathotypes of synovitis. These distinct biological signatures are promising for developing clinically applicable tools for decision in the selection of drugs for RA, albeit further validations in independent cohorts are required.
高效药物广泛可用于治疗类风湿关节炎(RA)。然而,准确选择可能对个体 RA 患者有效的药物一直具有挑战性。由于临床表型不可靠,无法指导药物选择,因此需要生物标志物。先前确定的用于预测治疗反应的遗传变异在 RA 患者的独立队列中未能复制。最近旨在发现预测治疗反应的生物标志物的研究侧重于综合组学分析,扩展到微生物组,并进一步更精细地定义滑膜病理类型。RA 患者的治疗反应者和无反应者可以通过其肠道微生物组组成、外周血转录组谱或滑膜炎的组织形态学和分子病理类型在基线时的不同特征来区分。这些不同的生物学特征很有希望为开发用于 RA 药物选择的临床应用工具提供依据,尽管还需要在独立队列中进行进一步验证。