Science and Research

Biomarkers of tissue remodeling predict survival in patients with pulmonary hypertension

BACKGROUND: Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are involved in vascular and right ventricular remodeling in pulmonary hypertension (PH). MMP2, MMP9, TIMP1, and TIMP4 were measured in plasma and their potential as biomarkers for PH was evaluated. METHODS: Consecutive patients undergoing right heart catheterization for suspected PH were included in this study (patients with mPAP >/=25mmHg were classed as having PH; those with mPAP <25mmHg served as non-PH controls). In total, 160 patients with PH (idiopathic pulmonary arterial hypertension, pulmonary arterial hypertension associated with connective tissue disease, chronic thromboembolic PH, and pulmonary venous hypertension) and 44 non-PH controls were included. Plasma from the time of PH diagnosis was analyzed for levels of MMP2, MMP9, TIMP1, and TIMP4 using enzyme immunoassays. Correlation analyses were performed with Pearson's or Spearman's coefficient, as appropriate. Mortality hazard ratios were derived using Cox regression analyses. RESULTS: Plasma levels of MMP2, MMP9, TIMP1, and TIMP4 showed considerable overlap between patient groups. In patients with PH, MMP2, TIMP1, and TIMP4 levels correlated with hemodynamic parameters (p<0.05) and six minute walking distance (p<0.01). Patients with high (>median) MMP2 and TIMP1 plasma levels had significantly worse 5-year survival than patients with low (
  • Tiede, S. L.; Wassenberg, M.; Christ, K.; Schermuly, R. T.; Seeger, W.; Grimminger, F.; Ghofrani, H. A.; Gall, H.
  • Keywords

    • Biomarker
    • Matrix metalloproteinases (MMPs)
    • Pulmonary hypertension
    • Survival
    • Tissue inhibitors of metalloproteinases (TIMPs)
    Publication details
    DOI: 10.1016/j.ijcard.2016.08.240
    Journal: International journal of cardiology
    Pages: 821-826 
    Work Type: Original
    Location: UGMLC
    Disease Area: PH
    Partner / Member: JLU
    Access-Number: 27575785
    See publication on PubMed


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