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Prevalence of myocardial perfusion abnormalities in end-stage liver disease
Ahmed Fathala1, Bander Safar, Ahmed Al Muhaideb
1Cardiovascular Imaging and Nuclear Medicine, Department of Medical Imaging Service, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. ahm35799@hotmail.com
Insights
The prevalence of abnormal myocardial perfusion scans (MPS) in end-stage liver disease (ESLD) patients awaiting liver transplantation is 8%. Diabetes and male gender are key predictors of abnormal MPS results, indicating potential coronary artery disease (CAD).
Area of Science:
- Cardiology
- Hepatology
- Nuclear Medicine
Background:
- Coronary artery disease (CAD) prevalence in end-stage liver disease (ESLD) patients undergoing evaluation for orthotopic liver transplantation (OLT) is not well-defined.
- Variable definitions for CAD contribute to the uncertainty regarding its prevalence in ESLD.
Purpose of the Study:
- To determine the prevalence of abnormal stress myocardial perfusion single-photon emission computed tomography (MPS) imaging as a marker for CAD in ESLD patients.
- To assess the utility of MPS as a routine pre-OLT workup for identifying CAD in this population.
Main Methods:
- A retrospective, single-center study reviewed data from 167 patients referred for stress MPS imaging before OLT.
- Patients were evaluated for traditional CAD risk factors including diabetes mellitus (DM), hypertension (HTN), hypercholesterolemia, age, and smoking status.
- Stress MPS was performed according to standard protocols.
Main Results:
- Out of 167 patients, 13 (8%) had abnormal MPS scans, while 147 (92%) had normal scans after excluding 7 non-diagnostic studies.
- Diabetes mellitus (DM) and male gender were identified as independent predictors of abnormal MPS (P=0.046 and P=0.26, respectively).
- No significant association was found between abnormal MPS and HTN, hypercholesterolemia, smoking, age, or liver disease etiology.
Conclusions:
- The prevalence of abnormal MPS, indicative of potential CAD, in ESLD patients evaluated for OLT is 8%.
- DM and male gender are significant independent predictors for abnormal MPS in this cohort.
- Further large-scale, randomized prospective studies are necessary to definitively establish the true prevalence of CAD and the role of MPS in ESLD patients awaiting OLT.
Background:
The prevalence of coronary artery disease (CAD) in end-stage liver disease (ESLD) being evaluated for orthotopic liver transplantation (OLT) is unclear based on variable definition used for CAD.
Objective:
The aim of this study to investigate the prevalence of abnormal stress myocardial perfusion single-photon emission computed tomography (MPS) imaging, as a marker for CAD, among patients with ESLD who were referred for stress MPS imaging as a routine work up before OLT.
Materials And Methods:
This was a single-center, retrospective study. We reviewed data on 167 patients who were referred for MPS as a routine work up before OLT over the last 2 years. All patients underwent evaluation for CAD risk factors [age, hypercholesterolemia, diabetes mellitus (DM), hypertension (HTN), and smoking], and stress MPS as per standard protocol.
Results:
The total number of patients referred for stress MPS was 167. Seven patients (4% of total study population) were excluded from the study due to poor and/or nondiagnostic studies. 147 patients (92%) had normal, but only 13 patients (8%) had abnormal MPS scans. DM and male gender were the most independent risk factors for abnormal MPS with P value of 0.046, and 0.26, respectively. There was no significant association between the abnormal MPS result and HTN, hypercholesterolemia, smoking, age or etiology of the liver disease.
Conclusion:
Based on our data, the prevalence of abnormal MPS and left ventricular ejection fraction in patients with ESLD was found to be 8%. DM and male gender were the most independent predictor factors for abnormal MPS. True prevalence of CAD and usefulness of MPS in patients with ESLD can only be studied using a very large and randomized prospective study.
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