Best Practice & Research Clinical Rheumatology
Volume 20, Issue 5 , Pages 849-863, October 2006

Treating very early rheumatoid arthritis

  • Karim Raza, MRCP, PhD (Clinical Senior Lecturer)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: 44 1214146778; Fax: 44 1214146794.
  • Mike Salmon, FRCPath, PhD (Professor of Experimental Rheumatology)

Rheumatology Research Group, Division of Immunity and Infection, Institute of Biomedical Research, MRC Centre for Immune Regulation, University of Birmingham, Birmingham B15 2TT, UK

Rheumatoid arthritis (RA) is common and leads to joint damage due to persistent synovitis. The persistence of inflammation is maintained by hyperplastic stromal tissue, which drives the accumulation of leukocytes in the synovium. Aggressive treatment after the first 3–4 months of symptoms, with either disease modifying anti-rheumatic drugs or anti-tumor necrosis factor (TNF)-α therapy, reduces the rate of disease progression. However, it rarely switches off disease such that remission can be maintained without the continued need for immunosuppressive therapy. There is increasing evidence that the first few months after symptom onset represent a pathologically distinct phase of disease. This very early phase may translate into a therapeutic window of opportunity during which it may be possible to permanently switch off the disease process. The rationale for, and approaches to, treatment within this very early window are discussed.

Key words: rheumatoid arthritis, early arthritis, synovitis, therapy, remission, DMARD, anti-TNF-α therapy

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PII: S1521-6942(06)00053-2

doi:10.1016/j.berh.2006.05.005

Best Practice & Research Clinical Rheumatology
Volume 20, Issue 5 , Pages 849-863, October 2006