Angiotensin-converting enzyme inhibitor therapy after heart transplant: From molecular basis to clinical effects

Daniele Masarone1, Ryan J Tedford2, Enrico Melillo1

  • 1Heart Failure Unit, Department of Cardiology, AORN dei Colli-Monaldi Hospital, Naples, Italy.

Insights

Angiotensin-converting enzyme inhibitors (ACEi) are vital for cardiovascular health, particularly in heart transplant recipients (HTRs) for managing hypertension and preventing complications. Further research is needed to confirm their broad clinical benefits in HTRs.

Area of Science:

  • Cardiovascular Medicine
  • Transplantation Immunology
  • Pharmacology

Background:

  • Angiotensin-converting enzyme inhibitors (ACEi) are established therapies for cardiovascular diseases like hypertension, ischemic heart disease, and heart failure (HF).
  • In heart transplant recipients (HTRs), ACEi are crucial for hypertension management, offering pleiotropic effects on vascular function and fluid balance.

Purpose of the Study:

  • To review the role and potential benefits of ACE inhibitors in heart transplant recipients.
  • To highlight the pleiotropic effects of ACEi in HTRs, including prevention of graft failure, cardiac allograft vasculopathy (CAV), and chronic kidney disease (CKD).

Main Methods:

  • Literature review of studies on ACE inhibitor use in cardiovascular diseases and heart transplant recipients.
  • Analysis of the molecular and clinical effects of ACEi in the context of HTRs.

Main Results:

  • ACEi demonstrate significant benefits in HTRs, including effective hypertension control and potential prevention of CAV and CKD progression.
  • ACEi exhibit pleiotropic effects, improving peripheral vascular function and regulating fluid and sodium balance.

Conclusions:

  • ACE inhibitors are a cornerstone therapy for HTRs, offering multifaceted benefits beyond blood pressure control.
  • Further multicenter, randomized studies are essential to validate the clinical efficacy of ACEi in HTRs and support wider adoption.
  • Investigating novel renin-angiotensin-aldosterone system inhibitors, like sacubitril, in HTRs is a promising future direction.

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