Donor myocardial HIF-1alpha is an independent predictor of cardiac allograft dysfunction: a 7-year prospective, exploratory study

Am J Transplant. 2007 Aug;7(8):2012-9. doi: 10.1111/j.1600-6143.2007.01875.x.

Abstract

Knowledge on interplay between the cardiac molecular response to transplantation-induced stress and primary graft dysfunction (PGD) is limited. A cDNA array identified HIF-1, EGR-1, NAB-2, VEGF-A and uPA as mediators of cardiac tissue response to transplantation-induced stress. mRNA expression of these molecules was measured in left ventricular biopsies from 200 donors before and after aortic cross-clamping and at 10-, 30- and 60-min reperfusion by real-time RT-PCR. HIF-1alpha expression at two time points was significantly associated with PGD, as shown by univariate analysis, receiver operating characteristic curve and multivariate logistic regression. At a cut-off level of 200 arbitrary units, HIF-1alpha after aortic cross-clamping in donors (78% sensitivity, 83% specificity) and at 10-min reperfusion (85% sensitivity, 83% specificity) identified PGD. HIF-1alpha demonstrates the potential to be a predictive marker for PGD; however, as multiple factors were tested at different time points, prospective evaluation is clearly necessary to confirm this observation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Biopsy
  • Echocardiography, Transesophageal
  • Female
  • Follow-Up Studies
  • Gene Expression*
  • Heart Failure / surgery
  • Heart Transplantation*
  • Heart Ventricles / metabolism
  • Heart Ventricles / pathology
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Male
  • Middle Aged
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Postoperative Complications
  • Prognosis
  • Prospective Studies
  • RNA, Messenger / genetics*
  • ROC Curve
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Tissue Donors*
  • Transplantation, Homologous
  • Ventricular Dysfunction, Left* / diagnosis
  • Ventricular Dysfunction, Left* / etiology
  • Ventricular Dysfunction, Left* / metabolism

Substances

  • Biomarkers
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Messenger