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Matrix metalloproteinases in coronary artery disease and myocardial infarction

  • Hanna Bräuninger
  • , Saskia Krüger
  • , Lucas Bacmeister
  • , Alexander Nyström
  • , Kilian Eyerich
  • , Dirk Westermann
  • , Diana Lindner
  • University Heart Center Freiburg
  • Partner Site Munich Heart Alliance
  • Universitätsklinikum Hamburg-Eppendorf
  • Albert-Ludwigs-Universität Freiburg

Research output: Contribution to journalReview articlepeer-review

74 Scopus citations

Abstract

Cardiovascular diseases (CVDs) remain the leading cause of death worldwide. Most cardiovascular deaths are caused by ischaemic heart diseases such as myocardial infarction (MI). Hereby atherosclerosis in the coronary arteries often precedes disease manifestation. Since tissue remodelling plays an important role in the development and progression of atherosclerosis as well as in outcome after MI, regulation of matrix metalloproteinases (MMPs) as the major ECM-degrading enzymes with diverse other functions is crucial. Here, we provide an overview of the expression profiles of MMPs in coronary artery and left ventricular tissue using publicly available data from whole tissue to single-cell resolution. To approach an association between MMP expression and the development and outcome of CVDs, we further review studies investigating polymorphisms in MMP genes since polymorphisms are known to have an impact on gene expression. This review therefore aims to shed light on the role of MMPs in atherosclerosis and MI by summarizing current knowledge from publically available datasets, human studies, and analyses of polymorphisms up to preclinical and clinical trials of pharmacological MMP inhibition.

Original languageEnglish
Article number18
JournalBasic Research in Cardiology
Volume118
Issue number1
DOIs
StatePublished - Dec 2023
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Atherosclerosis
  • Cardiac remodelling
  • Matrix metalloproteinases
  • Myocardial infarction
  • Single nucleotide polymorphisms
  • Single-cell sequencing data

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