Literature DB >> 31808123

Change in matrix metalloproteinase 2, 3, and 9 levels at the time of and after acute atherothrombotic myocardial infarction.

Ugochukwu Shola Owolabi1,2, Alok Ravindra Amraotkar1,3, Amanda R Coulter1,3, Narayana Sarma V Singam3, Bahjat N Aladili3, Ayesha Singh4, Patrick James Trainor3,5, Riten Mitra2, Andrew Paul DeFilippis6,7.   

Abstract

Elevated measures of matrix metalloproteinases (MMPs) are associated with acute myocardial infarction (MI), but it is not known how long these changes persist post-MI or if these measures differ between atherothrombotic versus non-atherothrombotic MI. MMPs-2, 3, and 9 were measured in 80 subjects with acute MI (atherothrombotic and non-atherothrombotic MI) or stable coronary artery disease (CAD). Measurements were made at, the time of acute MI, and > 3-month following acute MI (quiescent phase). Outcome measures were compared between groups and between time of acute MI and quiescent post-MI follow-up using Wilcoxon's and repeated measures analysis of variance. Forty-nine subjects met the criteria for acute MI with clearly defined atherothrombotic (n = 22) and non-atherothrombotic (n = 12) subsets. Fifteen subjects met criteria for stable CAD. MMP-3 was higher in acute MI versus stable CAD subjects at the time of acute MI: (453 vs. 217 pg/mL, p = 0.010) but not at quiescent phase follow-up (p > 0.05). MMP-9 was higher in acute MI versus stable CAD subjects at the time of acute MI: (412 vs. 168 pg/mL, p = 0.002) but not at the quiescent phase follow-up (p > 0.05). MMP-9 was higher at the time of acute MI versus quiescent phase follow-up in acute MI (412 vs. 213 pg/mL, p = 0.001) and atherothrombotic MI specifically (458 vs. 212 pg/mL, p = 0.001). No difference in MMP-2, 3, or 9 was observed between atherothrombotic versus non-atherothrombotic MI subgroups. MMPs-3 and 9 are significantly elevated in acute MI verses stable CAD subjects at time of acute MI but not different at quiescent phase follow-up. MMP-9 is elevated at the time of acute MI and specifically in acute atherothrombotic MI at time of MI versus quiescent phase follow-up.

Entities:  

Keywords:  Acute myocardial infarction; Atherothrombosis; Extracellular matrix; Metalloproteinases

Mesh:

Substances:

Year:  2020        PMID: 31808123      PMCID: PMC9012982          DOI: 10.1007/s11239-019-02004-7

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   5.221


  49 in total

1.  Presence of multiple coronary angiographic characteristics for the diagnosis of acute coronary thrombus.

Authors:  Alok R Amraotkar; Shahab Ghafghazi; Patrick J Trainor; Charles W Hargis; Affan B Irfan; Shesh N Rai; Aruni Bhatnagar; Andrew P DeFilippis
Journal:  Cardiol J       Date:  2017-02-02       Impact factor: 2.737

Review 2.  Matrix metalloproteinases and coronary artery disease: a novel therapeutic target.

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Journal:  J Clin Pharmacol       Date:  1997-11       Impact factor: 3.126

Review 3.  Fourth Universal Definition of Myocardial Infarction (2018).

Authors:  Kristian Thygesen; Joseph S Alpert; Allan S Jaffe; Bernard R Chaitman; Jeroen J Bax; David A Morrow; Harvey D White
Journal:  J Am Coll Cardiol       Date:  2018-08-25       Impact factor: 24.094

4.  Circulating levels of plasminogen and oxidized phospholipids bound to plasminogen distinguish between atherothrombotic and non-atherothrombotic myocardial infarction.

Authors:  Andrew P DeFilippis; Ilya Chernyavskiy; Alok R Amraotkar; Patrick J Trainor; Shalin Kothari; Imtiaz Ismail; Charles W Hargis; Frederick K Korley; Gregor Leibundgut; Sotirios Tsimikas; Shesh N Rai; Aruni Bhatnagar
Journal:  J Thromb Thrombolysis       Date:  2016-07       Impact factor: 2.300

5.  Carvedilol administration in acute myocardial infarction results in stronger inhibition of early markers of left ventricular remodeling than metoprolol.

Authors:  Giovanni Cimmino; Borja Ibanez; Chiara Giannarelli; Susanna Prat-González; Randolph Hutter; Mario Garcia; Javier Sanz; Valentin Fuster; Juan J Badimon
Journal:  Int J Cardiol       Date:  2010-09-22       Impact factor: 4.164

6.  Platelet Count and Mean Platelet Volume at the Time of and After Acute Myocardial Infarction.

Authors:  Alok Ravindra Amraotkar; David Day Song; Diana Otero; Patrick James Trainor; Imtiaz Ismail; Vallari Kothari; Ayesha Singh; Joseph B Moore; Shesh Nath Rai; Andrew Paul DeFilippis
Journal:  Clin Appl Thromb Hemost       Date:  2016-12-21       Impact factor: 2.389

Review 7.  Remodelling the extracellular matrix in development and disease.

Authors:  Caroline Bonnans; Jonathan Chou; Zena Werb
Journal:  Nat Rev Mol Cell Biol       Date:  2014-12       Impact factor: 94.444

Review 8.  Matrix metalloproteinases in cardiovascular disease.

Authors:  Peter Liu; Mei Sun; Sawsan Sader
Journal:  Can J Cardiol       Date:  2006-02       Impact factor: 5.223

9.  Usefulness of Plasma Matrix Metalloproteinase-3 Levels to Predict Myocardial Infarction in Men With and Without Acute Coronary Syndrome.

Authors:  Erdal Cavusoglu; Jonathan D Marmur; John T Kassotis; Sunitha Yanamadala; Vineet Chopra; Calvin Eng
Journal:  Am J Cardiol       Date:  2015-12-29       Impact factor: 2.778

10.  The Meaningfulness of Effect Sizes in Psychological Research: Differences Between Sub-Disciplines and the Impact of Potential Biases.

Authors:  Thomas Schäfer; Marcus A Schwarz
Journal:  Front Psychol       Date:  2019-04-11
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  3 in total

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Authors:  Andrew R Chapman; Yader Sandoval
Journal:  Clin Chem       Date:  2021-01-08       Impact factor: 8.327

2.  Circulating Matrix Metalloproteinase-28 Levels Are Related to GRACE Scores and Short-Term Outcomes in Patients with Acute Myocardial Infarction.

Authors:  Ke Zhou; Yuanmin Li; Yawei Xu; Rong Guo
Journal:  Biomed Res Int       Date:  2020-05-25       Impact factor: 3.411

Review 3.  Past, Present, and Future of Blood Biomarkers for the Diagnosis of Acute Myocardial Infarction-Promises and Challenges.

Authors:  Ioan Tilea; Andreea Varga; Razvan Constantin Serban
Journal:  Diagnostics (Basel)       Date:  2021-05-15
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