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Evaluation of Serum Matrix Metalloproteinase-3 as an Objective Indicator for the Disease Activity in Rheumatoid
Jina Yeo1,2, Han Joo Baek1, Yeong Wook Song2,3
1Division of Rheumatology, Department of Internal Medicine, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.
Objective:
This study aims to evaluate the change in serum metalloproteinase-3 (MMP-3) following the management of active rheumatoid arthritis (RA) and define the relationships between MMP-3 and disease activity indices.
Methods:
Data from a previously reported a 24-week, randomized controlled trial to investigate efficacy of tocilizumab in active RA refractory to methotrexate were analyzed. The serum level of MMP-3 were measured at week 0, 12, 20, and 24. The changes in MMP-3, and the relationship between MMP-3 and clinical parameters was assessed based on treatment group, methotrexate with or without tocilizumab.
Results:
A total of 95 patients were included in this study. The serum MMP-3 significantly decreased and showed similar pattern with other disease activity indices during treatment period in both treatment groups (p<0.001). The MMP-3 was positively correlated with ESR, CRP, DAS28, SDAI, and CDAI for 302 visits throughout 24 weeks (p<0.001). In another correlation analysis to evaluate the treatment effect at 24 week time point, methotrexate group showed significant correlation between serum markers MMP-3 (r=0.321, p=0.043); ESR (r=0.450, p=0.002); and CRP (r=0.536, p<0.001), with DAS28, but tocilizumab group didn't show meaningful correlation between serum markers and DAS28 (p>0.05).
Conclusion:
Serum MMP-3 showed positive correlation with disease activity indices in active RA patients. Furthermore, serum MMP-3 significantly decreased from baseline to week 20. As there is no single serum marker that can represent the disease activity particularly in tocilizumab treatment, MMP-3 might be a useful adjunct indicator to evaluate the treatment response in active RA patients.
Insights
Serum metalloproteinase-3 (MMP-3) levels decrease with rheumatoid arthritis (RA) treatment and correlate with disease activity. MMP-3 may serve as a useful indicator for treatment response in RA patients.
Area of Science:
- Rheumatology
- Biochemistry
- Clinical Medicine
Background:
- Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by joint inflammation and potential joint damage.
- Accurate monitoring of RA disease activity and treatment response is crucial for effective patient management.
- Serum metalloproteinase-3 (MMP-3) is an enzyme implicated in joint tissue remodeling and has been explored as a biomarker in RA.
Purpose of the Study:
- To evaluate changes in serum MMP-3 levels during active RA management.
- To determine the correlation between MMP-3 levels and established disease activity indices in RA.
- To assess the utility of MMP-3 as a potential biomarker for treatment response, particularly with tocilizumab therapy.
Main Methods:
- Analysis of data from a 24-week randomized controlled trial involving patients with active RA refractory to methotrexate.
- Measurement of serum MMP-3 levels at baseline and at weeks 12, 20, and 24.
- Assessment of changes in MMP-3 and its correlation with clinical parameters (ESR, CRP, DAS28, SDAI, CDAI) stratified by treatment group (methotrexate alone or with tocilizumab).
Main Results:
- Serum MMP-3 levels significantly decreased during the 24-week treatment period in both treatment groups (p<0.001).
- MMP-3 showed a positive correlation with ESR, CRP, DAS28, SDAI, and CDAI across 302 visits (p<0.001).
- At 24 weeks, the methotrexate group demonstrated significant correlations between MMP-3 and DAS28, while the tocilizumab group did not show meaningful correlations.
Conclusions:
- Serum MMP-3 is positively correlated with disease activity indices in patients with active RA.
- Serum MMP-3 levels significantly decrease from baseline by week 20 of treatment.
- MMP-3 may serve as a valuable adjunctive indicator for evaluating treatment response in active RA, especially when other serum markers lack clear correlation with disease activity during tocilizumab treatment.
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