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Updated: Nov 10, 2025

High-Resolution Cardiac Positron Emission Tomography/Computed Tomography for Small Animals
Published on: December 16, 2022
Dynamic FDG PET Imaging to Probe for Cardiac Metabolic Remodeling in Adults Born Premature
Philip A Corrado1, Gregory P Barton1,2,3, Francheska C Razalan-Krause4
1Department of Medical Physics, University of Wisconsin-Madison, Madison, WI 53705, USA.
Insights
Young adults born very premature do not show altered heart glucose metabolism at rest or during hypoxia. Further research is needed to determine if subtle metabolic changes predict future heart failure risk in this population.
Area of Science:
- Cardiology
- Metabolic Research
- Neonatal Medicine
Background:
- Individuals born very premature face elevated risks of cardiometabolic issues and heart failure.
- While structural heart changes in preterm infants are documented, metabolic underpinnings of this risk require investigation.
Purpose of the Study:
- To investigate myocardial glucose metabolism in young adults born preterm versus term-born individuals.
- To assess metabolic response to hypoxic stress in preterm-born adults.
Main Methods:
- Utilized dynamic fluorodeoxyglucose (FDG) positron emission tomography/magnetic resonance imaging (PET-MRI).
- Measured myocardial metabolic rate of glucose (MMRglc) under normoxic and hypoxic (12% O2) conditions.
- Calculated MMRglc using a 3-compartment kinetic model.
Main Results:
- Resting MMRglc was comparable between term and preterm groups.
- MMRglc decreased during hypoxia in both groups (p = 0.02).
- No significant differences in metabolic response to hypoxia were observed between groups, globally or within the myocardium.
Conclusions:
- No evidence of altered myocardial metabolism was found in healthy young adults born preterm.
- Subtle metabolic changes preceding or predicting heart failure in this population warrant further investigation.
Abstract:
Individuals born very premature have an increased cardiometabolic and heart failure risk. While the structural differences of the preterm heart are now well-described, metabolic insights into the physiologic mechanisms underpinning this risk are needed. Here, we used dynamic fluorodeoxyglucose (FDG) positron emission tomography/magnetic resonance imaging (PET-MRI) in young adults born term and preterm during normoxic (N = 28 preterm; 18 term) and hypoxic exposure (12% O2; N = 26 preterm; 17 term) to measure the myocardial metabolic rate of glucose (MMRglc) in young adults born term (N = 18) and preterm (N = 32), hypothesizing that young adults born preterm would have higher rates of MMRglc under normoxic conditions and a reduced ability to augment glucose metabolism under hypoxic conditions. MMRglc was calculated from the myocardial and blood pool time-activity curves by fitting the measured activities to the 3-compartment model of FDG kinetics. MMRglc was similar at rest between term and preterm subjects, and decreased during hypoxia exposure in both groups (p = 0.02 for MMRglc hypoxia effect). There were no differences observed between groups in the metabolic response to hypoxia, either globally (serum glucose and lactate measures) or within the myocardium. Thus, we did not find evidence of altered myocardial metabolism in the otherwise healthy preterm-born adult. However, whether subtle changes in myocardial metabolism may preceed or predict heart failure in this population remains to be determined.
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