Coronary microvascular dysfunction by positron emission tomography and outcomes in patients after cardiac

Bryan Abadie1, Yasmine Elghoul1, Sakthi Surya Prakash1

  • 1Department of Cardiovascular Medicine, Heart, Vascular, and Thoracic Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, J1-5 Main Campus, Cleveland, OH 44195, USA.

Insights

In cardiac transplant recipients without cardiac allograft vasculopathy (CAV), endogen/functional coronary microvascular dysfunction (CMD) identified by PET/CT is linked to increased mortality and adverse events. Classical/structural CMD did not show this association, suggesting PET/CT can refine risk stratification.

Area of Science:

  • Cardiology
  • Transplant Medicine
  • Medical Imaging

Background:

  • Cardiac allograft vasculopathy (CAV) impacts epicardial and microvascular coronary arteries.
  • Microvascular dysfunction in CAV is understudied.
  • PET/CT can screen for epicardial CAV, but implications of microvascular dysfunction without epicardial CAV are unclear.

Purpose of the Study:

  • To assess the prognostic significance of microvascular dysfunction subtypes using PET/CT.
  • To evaluate endogen/functional and classical/structural CMD in cardiac transplant patients without epicardial CAV.

Main Methods:

  • 356 transplant patients without prior CAV and normal perfusion imaging were analyzed.
  • Coronary microvascular dysfunction (CMD) defined as myocardial flow reserve < 2.0.
  • CMD subcategorized into endogen/functional (stress MBF ≥ 1.7) and classical/structural (stress MBF < 1.7).

Main Results:

  • 141 patients (39.6%) had CMD: 112 (31.4%) endogen/functional, 29 (8.1%) classical/structural.
  • Endogen/functional CMD associated with higher composite outcome (HR 2.39) and mortality (HR 2.98).
  • Classical/structural CMD showed no significant association with outcomes.

Conclusions:

  • Endogen/functional CMD in transplant patients without epicardial CAV predicts adverse events and mortality.
  • Classical/structural CMD pattern did not correlate with poor prognosis.
  • Integrating endogen/microvascular dysfunction assessment into PET/CT reporting can identify higher-risk patients.
Abstract