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Circulation. 2006;114:1020-1027
Published online before print August 21, 2006, doi: 10.1161/CIRCULATIONAHA.105.600353
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(Circulation. 2006;114:1020-1027.)
© 2006 American Heart Association, Inc.


Coronary Heart Disease

Specific Temporal Profile of Matrix Metalloproteinase Release Occurs in Patients After Myocardial Infarction

Relation to Left Ventricular Remodeling

Carson S. Webb, MD; David D. Bonnema, MD; S. Hinan Ahmed, MD; Amy H. Leonardi, BS; Catherine D. McClure, RDCS; Leslie L. Clark, MS; Robert E. Stroud, MS; William C. Corn, BA; Laura Finklea, RN; Michael R. Zile, MD; Francis G. Spinale, MD, PhD

From the Division of Cardiology, Department of Medicine (C.S.W., D.D.B., S.H.A., M.R.Z.), Department of Biostatistics, Bioinformatics and Epidemiology (L.L.C.), and Division of Cardiothoracic Surgery, Department of Surgery (A.H.L., C.D.M., L.L.C., R.E.S., W.C.C., L.F., F.G.S.), Medical University of South Carolina, and RHJ Department of Veterans Affairs Medical Center (M.R.Z., F.G.S.), Charleston, SC.

Correspondence to Francis G. Spinale, Cardiothoracic Surgery, Room 625, Strom Thurmond Research Bldg, 770 MUSC Complex, Medical University of South Carolina, 114 Doughty St, Charleston, SC 29425.

Received December 13, 2004; de novo received May 8, 2005; revision received June 13, 2006; accepted July 7, 2006.

Background— Changes in matrix metalloproteinase (MMP) and tissue inhibitors of MMPs (TIMPs) contribute to left ventricular (LV) remodeling after myocardial infarction (MI). We tested the hypothesis that a specific plasma MMP/TIMP profile would emerge after MI and be associated with the degree of LV dilation.

Methods and Results— LV end-diastolic volume and MMP/TIMP plasma profiles were determined in 53 age-matched control subjects and 32 post-MI patients from day 1 through 180 after MI. LV end-diastolic volume increased by >38% at day 90 after MI (P<0.05). MMP-9 increased by >150% from control at day 1 after MI (P<0.05) and remained elevated. MMP-8 rose to >120% at day 3 after MI (P<0.05) and fell to control values by day 5. TIMP-1 increased by >60% from control at day 1 after MI (P<0.05), whereas TIMP-2 increased only at later time points. Cardiac-specific TIMP-4 fell by 40% at day 5 after MI and remained reduced. A persistent or elevated MMP-9 at day 5 was accompanied by a 3-fold end-diastolic volume increase at day 28 (P<0.05).

Conclusions— A specific temporal pattern of MMP/TIMPs occurred in post-MI patients that included an early and robust rise in MMP-9 and MMP-8 and a uniform fall in TIMP-4. These findings suggest that a specific MMP/TIMP plasma profile occurs after MI and holds both prognostic and diagnostic significance.


 

CLINICAL PERSPECTIVE


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