Extracellular matrix collagen biomarker levels in patients who underwent pulmonary endarterectomy

Ahmet Zengin1, Rabia Kalkan2, Kübra Yıldız Aydın3

  • 1Department of Cardiovascular Surgery, University of Health Sciences, Kartal Koşuyolu Teaching and Education Hospital, Istanbul, Turkey.

Insights

Matrix metalloproteinase-9 (MMP-9) tissue levels were lower in chronic thromboembolic pulmonary hypertension (CTEPH) patients. Serum MMP-9 and MMP-2 levels did not differ, suggesting MMP-9 tissue levels may influence pulmonary vascular remodeling in CTEPH.

Area of Science:

  • Biochemistry
  • Pulmonary Medicine
  • Cardiovascular Research

Background:

  • The role of extracellular matrix collagen biomarkers in chronic thromboembolic pulmonary hypertension (CTEPH) remains unclear.
  • Matrix metalloproteinases (MMPs) are key enzymes involved in extracellular matrix remodeling.

Purpose of the Study:

  • To investigate the protein levels of matrix metalloproteinase (MMP)-2 and -9 in patients with CTEPH.
  • To explore the potential role of these biomarkers in the pathophysiology of CTEPH.

Main Methods:

  • Prospective, cross-sectional study comparing 24 CTEPH patients undergoing pulmonary endarterectomy with 24 controls undergoing lung surgery without pulmonary hypertension.
  • Serum MMP-9 levels and pulmonary artery tissue levels of MMP-2 (pro and active forms) and MMP-9 were measured using ELISA and Western blot techniques.

Main Results:

  • Serum MMP-9 concentrations were similar between CTEPH patients and controls.
  • Tissue levels of pro MMP-2/ß-actin and active MMP-2/ß-actin showed no significant difference between groups.
  • Tissue samples from CTEPH patients exhibited significantly lower levels of MMP-9/ß-actin compared to controls (P = 0.001).

Conclusions:

  • Serum extracellular matrix collagen biomarker levels are comparable in operable CTEPH patients and controls.
  • Reduced tissue levels of MMP-9/ß-actin may be implicated in pulmonary vascular remodeling in CTEPH patients eligible for surgery.
Abstract

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