» Articles » PMID: 21963570

Matrix Metalloproteinase-9 for the Earliest Stage Acute Coronary Syndrome

Overview
Journal Circ J
Date 2011 Oct 4
PMID 21963570
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Matrix metalloproteinase-9 (MMP-9) is regarded as a biomarker of plaque rupture or vulnerability and is elevated in patients with acute coronary syndrome (ACS). The aim of the present study was to evaluate the diagnostic value of MMP-9 for early ACS (≤4h of onset) and late ACS (>4h after onset), compared with high-sensitivity troponin T (hs-TnT).

Methods And Results: MMP-9 and hs-TnT were measured in 200 patients with ST elevation ACS (STEACS; 115 early STEACS and 85 late STEACS patients), and 66 patients with non-ST elevation ACS (NSTEACS; 25 early NSTEACS and 41 late NSTEACS patients). Forty patients with stable angina pectoris (SAP) were enrolled as a control group. MMP-9 levels were significantly higher in patients with early STEACS (P<0.001), early NSTEACS (P<0.001), late STEACS (P<0.001) and late NSTEACS (P=0.025) than SAP. MMP-9 levels were significantly higher in patients with early STEACS (P=0.017) and early NSTEACS (P=0.034) than late STEACS and late NSTEACS, respectively. Levels of hs-TnT were significantly lower in patients with early STEACS (P<0.001) and early NSTEACS (P=0.007) than late STEACS and late NSTEACS, respectively. On receiver operating characteristic curve analysis, area under the curve of early STEACS, early NSTEACS, late STEACS and late NSTEACS was 0.880, 0.782, 0.790 and 0.648 for MMP-9, and 0.707, 0.725, 0.993 and 0.920 for hs-TnT, respectively.

Conclusions: MMP-9 levels were elevated earlier than hs-TnT and had a higher diagnostic value for early ACS, but not for late ACS, reflecting plaque rupture or vulnerability.

Citing Articles

Effects of vasoactive substances on biomechanics of small resistance arteries of male and female Dahl salt-sensitive rats.

Mensah E, Daneshtalab N, Tabrizchi R Pharmacol Res Perspect. 2024; 12(2):e1180.

PMID: 38421097 PMC: 10902908. DOI: 10.1002/prp2.1180.


Sex-Related Differences of Matrix Metalloproteinases (MMPs): New Perspectives for These Biomarkers in Cardiovascular and Neurological Diseases.

Trentini A, Manfrinato M, Castellazzi M, Bellini T J Pers Med. 2022; 12(8).

PMID: 35893290 PMC: 9331234. DOI: 10.3390/jpm12081196.


Impact of MMP-9 Genetic Polymorphism and Concentration on the Development of Coronary Artery Disease in Ukrainian Population.

Pogorielova O, Korniienko V, Chumachenko Y, Obukhova O, Martsovenko I, Harbuzova V Cardiol Res Pract. 2022; 2022:2067632.

PMID: 35449607 PMC: 9017573. DOI: 10.1155/2022/2067632.


The Role of Matrix Metalloproteinase-9 in Atherosclerotic Plaque Instability.

Li T, Li X, Feng Y, Dong G, Wang Y, Yang J Mediators Inflamm. 2020; 2020:3872367.

PMID: 33082709 PMC: 7557896. DOI: 10.1155/2020/3872367.


Serum Matrix Metalloproteinase 9 and Macrophage Migration Inhibitory Factor (MIF) Are Increased in Young Healthy Nonobese Subjects with Positive Family History of Type 2 Diabetes.

Nikolajuk A, Matulewicz N, Stefanowicz M, Karczewska-Kupczewska M Int J Endocrinol. 2018; 2018:3470412.

PMID: 30302090 PMC: 6158960. DOI: 10.1155/2018/3470412.