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Donor plasma VEGF-A as a biomarker for myocardial injury and primary graft dysfunction after heart transplantation.
Holmström, Emil J; Syrjälä, Simo O; Dhaygude, Kishor; Tuuminen, Raimo; Krebs, Rainer; Lommi, Jyri; Nykänen, Antti; Lemström, Karl B.
Afiliação
  • Holmström EJ; Transplantation Laboratory, University of Helsinki, Helsinki, Finland; Cardiothoracic Surgery, Helsinki University Hospital, Helsinki, Finland. Electronic address: emil.j.holmstrom@helsinki.fi.
  • Syrjälä SO; Transplantation Laboratory, University of Helsinki, Helsinki, Finland; Cardiothoracic Surgery, Helsinki University Hospital, Helsinki, Finland.
  • Dhaygude K; Transplantation Laboratory, University of Helsinki, Helsinki, Finland.
  • Tuuminen R; Transplantation Laboratory, University of Helsinki, Helsinki, Finland.
  • Krebs R; Transplantation Laboratory, University of Helsinki, Helsinki, Finland.
  • Lommi J; Department of Cardiology, Helsinki University Hospital, Helsinki, Finland.
  • Nykänen A; Transplantation Laboratory, University of Helsinki, Helsinki, Finland; Cardiothoracic Surgery, Helsinki University Hospital, Helsinki, Finland.
  • Lemström KB; Transplantation Laboratory, University of Helsinki, Helsinki, Finland; Cardiothoracic Surgery, Helsinki University Hospital, Helsinki, Finland.
Article em En | MEDLINE | ID: mdl-38897424
ABSTRACT

BACKGROUND:

Vascular endothelial growth factor (VEGF)-A is an angiogenic and proinflammatory cytokine with profound effects on microvascular permeability and vasodilation. Several processes may induce VEGF-A expression in brain-dead organ donors. However, it remains unclear whether donor VEGF-A is linked to adverse outcomes after heart transplantation.

METHODS:

We examined plasma VEGF-A levels from 83 heart transplant donors as well as the clinical data of these donors and their respective recipients operated between 2010 and 2016. The donor plasma was analyzed using Luminex-based Multiplex and confirmed with a single-target ELISA. Based on donor VEGF-A plasma levels, the recipients were divided into 3 equal-sized groups (low VEGF <500 ng/liter, n = 28; moderate VEGF 500-3000 ng/liter, n = 28; and high VEGF >3000 ng/liter, n = 27). Biochemical and clinical parameters of myocardial injury as well as heart transplant and kidney function were followed-up for one year, while rejection episodes, development of cardiac allograft vasculopathy, and mortality were monitored for 5 years.

RESULTS:

Baseline parameters were comparable between the donor groups, except for age, where median ages of 40, 45, and 50 were observed for low, moderate, and high donor plasma VEGF levels groups, respectively, and therefore donor age was included as a confounding factor. High donor plasma VEGF-A levels were associated with pronounced myocardial injury (TnT and TnI), a higher inotrope score, and a higher incidence of primary graft dysfunction in the recipient after heart transplantation. Furthermore, recipients with allografts from donors with high plasma VEGF-A levels had a longer length of stay in the intensive care unit and the hospital, and an increased likelihood for prolonged renal replacement therapy.

CONCLUSIONS:

Our findings suggest that elevated donor plasma VEGF-A levels were associated with adverse outcomes in heart transplant recipients, particularly in terms of myocardial injury, primary graft dysfunction, and long-term renal complications. Donor VEGF-A may serve as a potential biomarker for predicting these adverse outcomes and identifying extended donor criteria.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Heart Lung Transplant Assunto da revista: CARDIOLOGIA / TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Heart Lung Transplant Assunto da revista: CARDIOLOGIA / TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article