Related Experiment Video
Updated: May 12, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
PET/CT with Myocardial Blood Flow Assessment Is Prognostic of Cardiac Allograft Vasculopathy Progression and Clinical
Nikil Prasad1, Erin Harris1, Ersilia M DeFilippis1
1Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, NewYork-Presbyterian Hospital, New York, New York.
Insights
Noninvasive cardiac allograft vasculopathy (CAV) assessment using 13N-ammonia PET/CT provides prognostic insights. This method offers high negative predictive value, potentially allowing extended intervals between invasive screenings for heart transplant recipients.
Area of Science:
- Cardiovascular Imaging and Nuclear Medicine
- Transplant Cardiology
- Medical Diagnostics
Background:
- Cardiac allograft vasculopathy (CAV) significantly increases morbidity and mortality post-heart transplant.
- Current diagnostic methods for CAV, including invasive coronary angiography (ICA), carry risks and necessitate frequent monitoring.
- There is a need for noninvasive methods to accurately assess CAV and predict patient outcomes.
Purpose of the Study:
- To evaluate the prognostic value of 13N-ammonia PET/CT myocardial perfusion imaging in assessing cardiac allograft vasculopathy (CAV) in heart transplant recipients.
- To determine the negative predictive value (NPV) of PET/CT for the development of moderate to severe CAV (ISHLT CAV 2/3) over extended intervals.
- To correlate PET/CT findings with clinical outcomes, including all-cause mortality and retransplantation.
Main Methods:
- 344 heart transplant recipients underwent 13N-ammonia PET/CT for CAV assessment, with data analyzed alongside invasive coronary angiography (ICA) using validated grading scales.
- CAV progression was tracked using serial ICA and PET/CT with myocardial blood flow reserve measurements at intervals of 600, 900, and 1200 days.
- Negative predictive values (NPVs) for CAV development were calculated, and hazard ratios were used to assess the risk of mortality and retransplantation associated with PET/CT findings.
Main Results:
- PET/CT grades 0/1 demonstrated high NPVs (0.93-0.95) for developing ISHLT CAV 2/3 on subsequent ICA.
- PET CAV grade 2/3 was associated with a 2.9-fold increased risk of all-cause mortality (HR 2.86). PET CAV grade 1 showed a numerically increased risk (HR 2.03).
- In a subgroup with stable CAV, PET CAV 2/3 remained significantly associated with increased risk of death or retransplantation (HR 3.20).
Conclusions:
- Noninvasive assessment of CAV using 13N-ammonia PET/CT and myocardial blood flow reserve provides valuable prognostic information.
- PET/CT demonstrates robust NPVs for predicting moderate to severe CAV, supporting the potential to extend surveillance intervals up to 4 years in select patients.
- These findings suggest that PET/CT can aid in optimizing monitoring strategies for heart transplant recipients, potentially reducing the need for frequent invasive procedures.
Abstract:
Cardiac allograft vasculopathy (CAV) causes impaired blood flow in both epicardial vessels and microvasculature and remains a leading cause of posttransplant morbidity and mortality. This study examined the prognostic value and outcomes of CAV, assessed by 13N-ammonia PET/CT myocardial perfusion imaging in heart transplant recipients. Methods: PET/CT and invasive coronary angiography (ICA) were graded using validated scales. CAV progression was assessed using intrapatient sequences: baseline ICA, interval PET/CT with myocardial blood flow reserve, and subsequent ICA. Intervals between ICAs of 600, 900, and 1200 d were included, and for each, the negative predictive value (NPV) of CAV development was assessed. Results: In total, 344 heart transplant recipients underwent PET/CT for CAV assessment with a median follow-up of 4.8 y. PET CAV grade 0/1 had an NPV of 0.93, 0.95, and 0.95 at each respective time point for developing an International Society for Heart and Lung Transplantation CAV 2/3 on subsequent ICA. Compared with PET CAV 0, PET CAV 2/3 was associated with a 2.9-fold increased risk of all-cause mortality (hazard ratio, 2.86; 95% CI, 1.36-6.00; P = 0.006). PET CAV 1 had a numerically increased risk (hazard ratio, 2.03; 95% CI, 0.99-4.15; P = 0.054). In a sensitivity analysis of 135 patients with stable International Society for Heart and Lung Transplantation CAV over successive ICA, PET CAV 2/3 remained associated with increased risk of death or retransplantation (hazard ratio, 3.20; 95% CI, 1.18-8.69; P = 0.03). Conclusion: Noninvasive CAV assessment by PET/CT and myocardial blood flow reserve provides prognostic information and robust NPVs for development of moderate to severe CAV over intervals up to 4 y. These data suggest that, for certain patients, intervals between invasive screenings may be extended.
Related Concept Videos
Imaging Studies for Cardiovascular System V: CT
Mitral Stenosis II: Clinical features and Diagnostic Tests
Acute Coronary Syndrome III: Diagnostic Studies

