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Early Assessment of Cardiac Allograft Vasculopathy Risk Among Recipients of Hepatitis C Virus-infected Donors in the
Kaushik Amancherla1, Irene D Feurer2, Scott A Rega3
1Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Insights
Heart transplants from hepatitis C virus (HCV)-positive donors did not show increased cardiac allograft vasculopathy (CAV) risk in the direct-acting antiviral era. Further studies are needed to confirm these findings and guide post-transplant care.
Area of Science:
- Cardiology
- Transplantation Immunology
- Infectious Diseases
Background:
- Direct-acting antiviral (DAA) therapies have revolutionized hepatitis C virus (HCV) treatment, leading to increased use of HCV-positive donor organs for transplantation.
- Historically, HCV-positive donors were associated with accelerated cardiac allograft vasculopathy (CAV).
- The impact of HCV nucleic acid test-positive (NAT+) donors on CAV in the DAA era is not well understood.
Purpose of the Study:
- To investigate the association between HCV NAT+ donor heart transplantation and the development of CAV in the DAA era.
- To compare CAV outcomes between recipients of HCV NAT+ and HCV NAT- donor hearts within the first year post-transplant.
Main Methods:
- Retrospective, single-center observational study.
- Compared 84 recipients of HCV NAT+ donor hearts with 231 recipients of HCV NAT- donor hearts.
- Utilized coronary angiography and intravascular ultrasound to assess CAV development, including rapidly progressive CAV.
Main Results:
- Unadjusted analysis showed reduced survival free of CAV in recipients of HCV NAT+ hearts.
- After adjusting for known CAV risk factors, no significant difference in CAV development was observed between the HCV NAT+ and NAT- cohorts.
- No significant difference in the development of rapidly progressive CAV was found between the groups.
Conclusions:
- Transplantation of hearts from HCV NAT+ donors does not appear to increase CAV risk in the DAA era.
- Larger, longer-term studies are recommended to confirm these findings.
- Further research will inform post-transplant management strategies for recipients of HCV NAT+ donor hearts.
Background:
Transplantation of hearts from hepatitis C virus (HCV)-positive donors has increased substantially in recent years following development of highly effective direct-acting antiviral therapies for treatment and cure of HCV. Although historical data from the pre-direct-acting antiviral era demonstrated an association between HCV-positive donors and accelerated cardiac allograft vasculopathy (CAV) in recipients, the relationship between the use of HCV nucleic acid test-positive (NAT+) donors and the development of CAV in the direct-acting antiviral era remains unclear.
Methods And Results:
We performed a retrospective, single-center observational study comparing coronary angiographic CAV outcomes during the first year after transplant in 84 heart transplant recipients of HCV NAT+ donors and 231 recipients of HCV NAT- donors. Additionally, in a subsample of 149 patients (including 55 in the NAT+ cohort and 94 in the NAT- cohort) who had serial adjunctive intravascular ultrasound examination performed, we compared development of rapidly progressive CAV, defined as an increase in maximal intimal thickening of ≥0.5 mm in matched vessel segments during the first year post-transplant. In an unadjusted analysis, recipients of HCV NAT+ hearts had reduced survival free of CAV ≥1 over the first year after heart transplant compared with recipients of HCV NAT- hearts. After adjustment for known CAV risk factors, however, there was no significant difference between cohorts in the likelihood of the primary outcome, nor was there a difference in development of rapidly progressive CAV.
Conclusions:
These findings support larger, longer-term follow-up studies to better elucidate CAV outcomes in recipients of HCV NAT+ hearts and to inform post-transplant management strategies.
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