
doi: 10.1038/nrdp.2018.1
pmid: 29417936
Rheumatoid arthritis (RA) is a chronic, inflammatory, autoimmune disease that primarily affects the joints and is associated with autoantibodies that target various molecules including modified self-epitopes. The identification of novel autoantibodies has improved diagnostic accuracy, and newly developed classification criteria facilitate the recognition and study of the disease early in its course. New clinical assessment tools are able to better characterize disease activity states, which are correlated with progression of damage and disability, and permit improved follow-up. In addition, better understanding of the pathogenesis of RA through recognition of key cells and cytokines has led to the development of targeted disease-modifying antirheumatic drugs. Altogether, the improved understanding of the pathogenetic processes involved, rational use of established drugs and development of new drugs and reliable assessment tools have drastically altered the lives of individuals with RA over the past 2 decades. Current strategies strive for early referral, early diagnosis and early start of effective therapy aimed at remission or, at the least, low disease activity, with rapid adaptation of treatment if this target is not reached. This treat-to-target approach prevents progression of joint damage and optimizes physical functioning, work and social participation. In this Primer, we discuss the epidemiology, pathophysiology, diagnosis and management of RA.
Epigenomics, Arthritis, Rheumatoid, Early Diagnosis, Methotrexate, Risk Factors, Antirheumatic Agents, Disease Progression, Quality of Life, Humans, Mass Screening, Glucocorticoids
Epigenomics, Arthritis, Rheumatoid, Early Diagnosis, Methotrexate, Risk Factors, Antirheumatic Agents, Disease Progression, Quality of Life, Humans, Mass Screening, Glucocorticoids
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