PMID- 9779299 OWN - NLM STAT- MEDLINE DCOM- 19981209 LR - 20220409 IS - 0392-856X (Print) IS - 0392-856X (Linking) VI - 16 IP - 5 DP - 1998 Sep-Oct TI - Serum matrix metalloproteinase-3 and fibrin degradation product levels correlate with clinical disease activity in rheumatoid arthritis. PG - 533-40 AB - OBJECTIVE: Plasmin and matrix metalloproteinase-3 (MMP-3) have been linked to articular destruction in rheumatoid arthritis (RA). We compared circulating levels of plasmin-mediated fibrin degradation product (FDP D-dimer) and MMP-3 with traditional parameters of disease activity in RA to determine their clinical utility. MATERIALS AND METHODS: Serum levels of MMP-3 and D-dimer were determined by enzyme-linked immunoassays in 60 patients with RA. Twenty healthy females and 21 patients with systemic lupus erythematosus (SLE) served as controls. RESULTS: MMP-3 (436.8 +/- 474.2 ng/ml) and D-dimer levels (351.2 +/- 296.3 ng/ml) were markedly elevated in the sera from RA patients as compared with healthy controls (43.9 +/- 15.2 ng/ml and 63.0 +/- 64.1 ng/ml, p < 0.0001, respectively). Both levels strongly correlated with each other (r = 0.627, p < 0.0001) and were closely associated with various clinical parameters for the disease activity of RA, including the erythrocyte sedimentation rate (ESR) and the Lansbury's activity index (p < 0.0001). MMP-3 levels were more highly correlated with articular parameters such as the swollen and painful joint counts (r = 0.454, p = 0.0002), whereas D-dimer levels correlated well with C-reactive protein (CRP) levels (r = 0.581, p < 0.0001). In SLE patients, MMP-3 (239.1 +/- 199.6 ng/ml, p < 0.0001) and D-dimer levels (86.9 +/- 85.2 ng/ml, p = 0.0278) were also higher than in healthy controls. Both levels correlated with each other (r = 0.612, p = 0.0025), and were associated with ESR and CRP levels, as was observed in RA patients, but not with most of the other clinical indicators for SLE. CONCLUSIONS: Serum levels of MMP-3 and D-dimer are clinically useful indicators for disease activity in RA. Our results further support the hypothesis that MMP-3 and plasmin may interact in the inflammatory synovial tissues, and thus augment the articular destruction seen in RA. In SLE patients, however, MMP-3 producing cells could be different from in RA patients, and further studies will be required to clarify the pathogenetic mechanism underlying the raised serum levels of MMP-3 and/or D-dimer. FAU - Ichikawa, Y AU - Ichikawa Y AD - Department of Internal Medicine 4, Tokai University School of Medicine, Kanagawa, Japan. FAU - Yamada, C AU - Yamada C FAU - Horiki, T AU - Horiki T FAU - Hoshina, Y AU - Hoshina Y FAU - Uchiyama, M AU - Uchiyama M LA - eng PT - Comparative Study PT - Journal Article PL - Italy TA - Clin Exp Rheumatol JT - Clinical and experimental rheumatology JID - 8308521 RN - 0 (Antifibrinolytic Agents) RN - 0 (Biomarkers) RN - 0 (Fibrin Fibrinogen Degradation Products) RN - 0 (fibrin fragment D) RN - 9007-41-4 (C-Reactive Protein) RN - EC 3.4.24.17 (Matrix Metalloproteinase 3) SB - IM MH - Adult MH - Aged MH - Antifibrinolytic Agents/*blood MH - Arthritis, Rheumatoid/*blood/*physiopathology MH - Biomarkers MH - Blood Sedimentation MH - C-Reactive Protein/analysis MH - Female MH - Fibrin Fibrinogen Degradation Products/*analysis MH - Humans MH - Lupus Erythematosus, Systemic/blood/physiopathology MH - Male MH - Matrix Metalloproteinase 3/*blood MH - Middle Aged MH - Severity of Illness Index EDAT- 1998/10/21 00:00 MHDA- 1998/10/21 00:01 CRDT- 1998/10/21 00:00 PHST- 1998/10/21 00:00 [pubmed] PHST- 1998/10/21 00:01 [medline] PHST- 1998/10/21 00:00 [entrez] PST - ppublish SO - Clin Exp Rheumatol. 1998 Sep-Oct;16(5):533-40.