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.

PubMed
Abstract

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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