类风湿性关节炎
滑膜炎
医学
个性化医疗
微生物群
转录组
精密医学
仿形(计算机编程)
生物信息学
计算生物学
药物反应
药品
内科学
生物
药理学
病理
基因
遗传学
计算机科学
基因表达
操作系统
作者
Monica Wei,Cong‐Qiu Chu
标识
DOI:10.1016/j.berh.2021.101741
摘要
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.
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