Usefulness of Plasma Matrix Metalloproteinase-3 Levels to Predict Myocardial Infarction in Men With and Without Acute
Erdal Cavusoglu1, Jonathan D Marmur2, John T Kassotis2
1Division of Cardiology, Department of Medicine, Bronx Veterans Affairs Medical Center, Bronx, New York; Division of Cardiology, Department of Medicine, State University of New York Downstate Medical Center, Brooklyn, New York.
Abstract:
Matrix metalloproteinase-3 (MMP-3), or stromelysin-1, is a matrix metalloproteinase which is expressed in atherosclerotic plaques and which has been implicated in the pathogenesis of acute coronary syndrome (ACS). Functional polymorphisms in the promoter region of the human MMP-3 gene resulting in an increased expression of MMP-3 have been shown to predict the risk of incident myocardial infarction (MI). However, there have been no studies that have specifically examined the utility of baseline plasma MMP-3 levels for the prediction of long-term MI. In this study, baseline plasma MMP-3 levels were measured in 355 male patients who were referred for coronary angiography and followed prospectively for the development of enzymatically confirmed MI out to 5 years. After adjustment for a variety of baseline clinical, angiographic, and laboratory parameters, plasma MMP-3 levels were an independent predictor of MI at 5 years (hazards ratio 1.42, 95% CI 1.13 to 1.79; p = 0.0023). Furthermore, in 5 additional multivariate models that included a variety of contemporary biomarkers associated with adverse outcomes and MI, MMP-3 remained an independent predictor of MI at 5 years. Similar results were obtained when the analyses were restricted to the subpopulation of patients presenting with ACS. In conclusion, elevated levels of MMP-3 are associated with an increased risk of long-term MI in patients with and without ACS referred for coronary angiography. Furthermore, this association is independent of a variety of clinical, angiographic, laboratory variables, including biomarkers with established prognostic efficacy for the prediction of MI.
Insights
Elevated matrix metalloproteinase-3 (MMP-3) levels predict long-term myocardial infarction (MI) risk in patients undergoing coronary angiography. This finding holds true even for those without acute coronary syndrome (ACS).
Area of Science:
- Cardiovascular Medicine
- Biomarker Research
- Proteomics
Background:
- Matrix metalloproteinase-3 (MMP-3), also known as stromelysin-1, is present in atherosclerotic plaques and linked to acute coronary syndrome (ACS) pathogenesis.
- Genetic variations affecting MMP-3 expression correlate with myocardial infarction (MI) risk, but baseline plasma levels' predictive value for long-term MI remains unexamined.
Purpose of the Study:
- To investigate the utility of baseline plasma MMP-3 levels in predicting long-term MI risk.
- To assess MMP-3's predictive power in patients with and without ACS referred for coronary angiography.
Main Methods:
- Prospective study of 355 male patients undergoing coronary angiography.
- Measurement of baseline plasma MMP-3 levels.
- Follow-up for up to 5 years for enzymatically confirmed MI.
- Statistical analysis including multivariate models adjusted for clinical, angiographic, and laboratory parameters, and other biomarkers.
Main Results:
- Elevated baseline plasma MMP-3 levels independently predicted MI over 5 years (HR 1.42, 95% CI 1.13-1.79, p=0.0023).
- MMP-3 remained a significant predictor even after adjusting for multiple clinical and laboratory variables, including established MI biomarkers.
- Similar predictive value was observed in the subgroup of patients presenting with ACS.
Conclusions:
- Baseline plasma MMP-3 levels are an independent predictor of long-term MI risk in patients undergoing coronary angiography, irrespective of ACS status.
- The prognostic value of MMP-3 is robust and independent of other established risk factors and biomarkers for MI prediction.
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