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Updated: Dec 15, 2025

Non-invasive Imaging of Acute Allograft Rejection after Rat Renal Transplantation Using 18F-FDG PET
Published on: April 28, 2013
Myocardial ischemia by radionuclide imaging and long-term outcomes after kidney transplantation
Sanmay Low1,2, Horng-Ruey Chua3,4, Raymond Wong5,6
1Department of Medicine, Level 10 Medicine Office, National University Centre for Organ Transplantation, National University Hospital, National University Health System, NUHS Tower Block, 1E Kent Ridge Road, Singapore, 119228, Republic of Singapore.
Purpose:
We examined the incidence of myocardial ischemia (MI) in kidney transplant recipients (KTR) using myocardial perfusion imaging (MPI), and its association with long-term outcomes after transplantation.
Methods:
A retrospective observational study was conducted of asymptomatic KTRs who underwent post-transplant MPI screening for MI, as defined by moderate to severe myocardial perfusion defects, post-stress myocardial stunning or balanced ischemia. A composite outcome of all-cause mortality, graft loss, and major adverse cardiovascular events (MACE) was examined over minimum 5 years.
Results:
We studied 135 KTRs who underwent 226 MPIs, with follow-up duration of 10 (7-13) years. 110 (81%) patients had normal MPIs, 11 (8%) had mild perfusion defects, and 14 (10%) had MI. Correspondingly, composite outcome developed in 6%, 27%, and 43% (p = 0.04), and MACE occurred in 7%, 0%, and 21% (p = 0.11), of the respective subgroups. Twenty-six patients developed the composite outcome after 5 (3-7) years post-transplantation, including 11 patients with MACE. On multivariate analysis, MI, higher low-density lipoprotein levels, and proteinuria > 0.3 g/day independently predicted the composite outcome; only MI predicted MACE (all p < 0.05). Ninety-one patients had two serial MPIs, which increased the positive predictive value for MACE from 17 to 25%. Absence of MI had negative predictive value of 83% for MACE and 93% for the composite outcome.
Conclusion:
MI that is detected early post-kidney transplantation predicts long-term mortality, graft loss, and MACE in KTRs, with excellent negative but poor positive predictive values.
Insights
Myocardial ischemia (MI) detected early after kidney transplantation in recipients (KTRs) predicts poor long-term outcomes, including mortality and graft loss. Early MI identification is crucial for risk stratification in KTRs.
Area of Science:
- Cardiology
- Nephrology
- Transplantation Medicine
Background:
- Kidney transplant recipients (KTRs) face significant cardiovascular risks.
- Early detection of myocardial ischemia (MI) is vital for improving long-term outcomes in KTRs.
Purpose of the Study:
- To determine the incidence of MI in KTRs using myocardial perfusion imaging (MPI).
- To assess the association between early post-transplant MI and long-term outcomes, including mortality, graft loss, and major adverse cardiovascular events (MACE).
Main Methods:
- A retrospective observational study of asymptomatic KTRs undergoing post-transplant MPI screening.
- MI defined by moderate to severe perfusion defects, post-stress stunning, or balanced ischemia.
- Composite outcome of all-cause mortality, graft loss, and MACE analyzed over a minimum of 5 years.
Main Results:
- 135 KTRs with 226 MPIs and 10 years follow-up were analyzed.
- 10% of KTRs had MI; these patients showed significantly higher rates of composite outcomes (43%) and MACE (21%) compared to those without MI.
- MI, high LDL, and proteinuria independently predicted composite outcomes; MI alone predicted MACE.
Conclusions:
- Early detected MI post-kidney transplantation is a significant predictor of adverse long-term outcomes in KTRs.
- MPI demonstrates excellent negative predictive value for MACE and composite outcomes.
- While MI has poor positive predictive value, its presence warrants close monitoring and risk management in KTRs.
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Kidney Transplant I: Introduction
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Acute Kidney Injury IV: Diagnostic Studies and Prevention
Acute Coronary Syndrome III: Diagnostic Studies
Imaging Studies for Cardiovascular System IV: CMRI

