Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3342981 | Best Practice & Research Clinical Rheumatology | 2010 | 13 Pages |
In rheumatoid arthritis (RA), early use of disease-modifying anti-rheumatic drugs (DMARDs), intensive follow-up and ‘treating to target’ to achieve low disease activity produce significant improvements in measures of disease activity, functional impairment and retard erosive radiographic progression. Step-up, parallel and step-down regimens are all significantly more effective than sequential monotherapy; although the most effective regimen has not been established. Minimising the period of exposure to synovitis, by including a rapidly acting agent (e.g., corticosteroids or tumour necrosis factor α (TNFα) inhibitor), may slow radiographic progression further. Biologic therapies, especially TNFα inhibitors, are effective in early RA; however, their exact role is unclear. Current measures may overestimate the number of patients in clinical remission; therefore, musculoskeletal ultrasound and/or novel biomarkers may also have a role. Pre-clinical immunological markers could possibly be used to trigger pre-emptive treatment in asymptomatic, ‘at risk’ individuals. Potential treatment developments include combining biologic agents or targeting alternative immunological pathways.