Metalloproteinases and Hypertrophic Cardiomyopathy: A Systematic Review

Giuseppe Filiberto Serraino1, Federica Jiritano1, Davide Costa2

  • 1Department of Experimental and Clinical Medicine, "Magna Graecia" University of Catanzaro, 88100 Catanzaro, Italy.

Biomolecules
|May 16, 2023
PubMed

Insights

Matrix metalloproteinases (MMPs) are elevated in hypertrophic cardiomyopathy (HCM) patients. Monitoring MMPs and their inhibitors (TIMPs) may offer a non-invasive method for evaluating HCM progression and treatment effectiveness.

Area of Science:

  • Cardiovascular Research
  • Biochemistry
  • Genetics

Background:

  • Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by abnormal extracellular matrix collagen turnover.
  • Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) show altered release patterns in HCM patients.

Approach:

  • A systematic review was conducted to consolidate current knowledge on MMP profiles in HCM.
  • Literature screening spanned from July 1975 to November 2022, selecting 16 trials with 892 participants meeting inclusion criteria.

Key Points:

  • MMP levels, particularly MMP2, were significantly higher in HCM patients compared to healthy controls.
  • MMPs have been utilized as biomarkers to assess outcomes following surgical and percutaneous interventions in HCM.
  • Altered collagen turnover in the cardiac extracellular matrix is a hallmark of HCM.

Conclusions:

  • Understanding the molecular regulation of cardiac extracellular matrix collagen turnover is crucial for HCM management.
  • Monitoring MMPs and TIMPs presents a potential avenue for non-invasive evaluation and assessment of hypertrophic cardiomyopathy.

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