Donor Age, Sex, and Cause of Death and Their Relationship to Heart Transplant Recipient Cardiac Death

Author:

Hammond Margo1,Zollinger Charles2,Vidic Andrija3ORCID,Snow Gregory4,Stehlik Josef5,Alharethi Rami6,Kfoury Abdallah6,Drakos Stavros5,Hammond M56

Affiliation:

1. Department of Biochemistry, Brigham Young University, Provo, UT 84602, USA

2. Intermountain Donor Services, 6065 S Fashion Blvd, Murray, UT 84107, USA

3. Department of Cardiology, University of Kansas Hospital, 4000 Cambridge St., Kansas City, KS 66160, USA

4. Department of Statistics, Brigham Young University, Provo, UT 84602, USA

5. Department of Cardiology, University of Utah Hospital, 50 N Medical Drive, Salt Lake City, UT 84132, USA

6. Cardiac Transplant Program, Intermountain Medical Center, 5252 S Intermountain Drive, Salt Lake City, UT 84157, USA

Abstract

Background: Recent studies indicate that donor innate immune responses participate in initiating and accelerating innate responses and allorecognition in the recipient. These immune responses negatively affect recipient outcomes and predispose recipients to cardiovascular death (CV death). We hypothesized that a donor cause of death (COD) associated with higher levels of innate immune response would predispose recipients to more adverse outcomes post-transplant, including CV death. Methods: We performed a single-institution retrospective analysis comparing donor characteristics and COD to recipient adverse cardiovascular outcomes. We analyzed the medical records of local adult donors (age 18–64) in a database of donors where adequate data was available. Donor age was available on 706 donors; donor sex was available on 730 donors. We linked donor characteristics (age and sex) and COD to recipient CV death. The data were analyzed using logistic regression, the log-rank test of differences, and Tukey contrast. Results: Donor age, female sex, and COD of intracranial hemorrhage were significantly associated with a higher incidence of recipient CV death. Conclusions: In this single institution study, we found that recipients with hearts from donors over 40 years, donors who were female, or donors who died with a COD of intracranial hemorrhage had a higher frequency of CV death. Donor monitoring and potential treatment of innate immune activation may decrease subsequent recipient innate responses and allorecognition stimulated by donor-derived inflammatory signaling, which leads to adverse outcomes.

Funder

A. Lee Christensen Fund of the Intermountain Medical and Research Foundation, Salt Lake City, Utah

Publisher

MDPI AG

Subject

General Medicine

Reference34 articles.

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3. Cardiac allograft vasculopathy: Current review and future research directions;Pober;Cardiovasc. Res.,2021

4. Transplantation and damage-associated molecular patterns (DAMPs);Land;Am. J. Transplant.,2016

5. Immune regulation by microvascular endothelial cells: Directing innate and adaptive immunity, coagulation, and inflammation;Danese;J. Immunol.,2007

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