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Elevated circulating levels of matrix metalloproteinase-9 and -2 in patients with symptomatic coronary artery disease

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Abstract:

Abstract Background: 

Matrix metalloproteinases (MMP-9 and MMP-2) have been implicated in development of atherosclerosis and plaque rupture in acute coronary syndromes (ACS). Aim: 

To determine the relationship between circulating MMPs and symptomatic coronary artery disease. Methods: 

Plasma levels of MMP-9 and MMP-2 were measured in patients with ACS, stable angina (SA) and in controls, using a quantitative gelatin zymography. These measurements were correlated with markers of systemic inflammation (hs-CRP) in all subjects and myocardial injury (troponin T) in patients with ACS. Results: 

Plasma MMP-9 in ACS was greater than in SA, and was greater in SA than in controls (P < 0.01 ACS vs SA and controls, P < 0.01 SA vs control). Plasma MMP-2 was significantly greater in ACS than SA or controls (P < 0.01 vs SA and controls). There was strong overall relationship between hs-CRP and MMP-9 (r = 0.65, P < 0.0001) driven by a significant relationship in ACS patients (r = 0.58, P = 0.02), as there was no significant association in SA or controls. A weaker overall correlation was found between hs-CRP and MMP-2 (r = 0.39, P = 0.02), but no significant relationship was present for either of the two patient subgroups or controls. There was no correlation between levels of troponin T and MMP-9, MMP-2 or hs-CRP in ACS patients. Conclusion: 

Quantitative gelatin zymography identifies increased circulating levels of MMP-9 and MMP-2 in patients with symptomatic coronary disease. MMP-9 and MMP-2 are higher in ACS than SA patients and might have use as markers of plaque rupture or instability. The strong relationship between MMP-9 and hs-CRP in ACS patients suggests MMP-9 might be an additional marker and/or consequence of the inflammatory component in ACS. (Intern Med J 2005; 35: 331–335)

Keywords: coronary artery disease; inflammation; matrix metalloproteinase; myocardial injury; zymography

Document Type: Research Article

DOI: http://dx.doi.org/10.1111/j.1445-5994.2005.00822.x

Affiliations: Department of Cardiology, Concord Hospital, Vascular Biology Laboratory, ANZAC Research Institute, University of Sydney, Sydney, Australia

Publication date: June 1, 2005

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