Abstract
Objective. To determine the effects of treatment with sulfasalazine (SSZ) or the combination of methotrexate (MTX) and SSZ on serum matrix metalloproteinase 3 (MMP-3) levels in patients with early rheumatoid arthritis (RA).
Methods. Eighty-two patients with early RA (symptoms <1 year and DMARD-naive at presentation) were selected who had been treated with SSZ (2000 mg/day) or with the combination of MTX (7.5-15 mg/week) and SSZ. Serum MMP-3 levels, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), swollen joint count (SJC), tender joint count (TJC), Ritchie articular index (RAI), and the Disease Activity Score (DAS) were determined at 4 week intervals during a followup of 28 weeks for each treatment group. Response was based on clinical grounds and CRP at 12, 20, and 28 weeks.
Results. SSZ responders (n = 52) had lower baseline values of serum MMP-3, CRP, and ESR, compared to partial/nonresponders (n = 30). but did not differ in joint scores and DAS. In the SSZ responder group all variables decreased. In the SSZ partial/nonresponders, CRP, ESR, and SJC decreased in contrast to serum MMP-3, TJC, RAI, and DAS-3. After addition of MTX all variables decreased in 24 of the 30 patients who had shown a partial or no response taking SSZ. In the SSZ responders there was a delayed decrease in serum MMP-3 compared to CRP.
Conclusion. Serum MMP-3 levels decrease in patients with early RA who respond to SSZ or to the combination of MTX and SSZ. In patients who respond to SSZ the changes in serum MMP-3 levels indicate a delayed response compared to CRP.
| Original language | English |
|---|---|
| Pages (from-to) | 883-889 |
| Number of pages | 7 |
| Journal | Journal of Rheumatology |
| Volume | 29 |
| Issue number | 5 |
| Publication status | Published - May-2002 |
Keywords
- serum matrix metalloproteinase 3
- stromelysin 1
- early rheumatoid arthritis
- disease modifying antirheumatic drugs
- sulfasalazine
- methotrexate
- COLLAGEN-INDUCED ARTHRITIS
- FACTOR-KAPPA-B
- TISSUE INHIBITOR
- DISEASE-ACTIVITY
- SYSTEMIC INFLAMMATION
- CARTILAGE DESTRUCTION
- STROMELYSIN
- MECHANISMS
- FIBROBLASTS
- PROGRESSION
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