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Magnetic Resonance Imaging-Derived Microvascular Perfusion Modeling to Assess Peripheral Artery Disease
Olga A Gimnich1, Tatiana Belousova2, Christina M Short3
1Penn State Heart and Vascular Institute, Pennsylvania State University College of Medicine Hershey PA.
Journal of the American Heart Association
|January 23, 2023
Summary
A new computational model of microvascular perfusion accurately distinguishes patients with peripheral artery disease (PAD) from controls. This model shows promise for studying lower extremity ischemia and assessing disease severity.
Area of Science:
- Biomedical Engineering
- Medical Imaging
- Computational Biology
Background:
- Computational fluid dynamics (CFD) models align well with contrast-enhanced magnetic resonance imaging (CE-MRI) in cardiovascular applications.
- Microvascular dysfunction is a key factor in peripheral artery disease (PAD) affecting skeletal muscle perfusion.
- Developing advanced computational models is crucial for understanding microvascular behavior in disease states.
Purpose of the Study:
- To develop and validate a biomechanical model of microvascular perfusion in skeletal calf muscles using CE-MRI data.
- To investigate differences in microvascular parameters between patients with PAD and healthy controls.
- To assess the association of computational microvascular model parameters with clinical markers of PAD severity and exercise capacity.
Main Methods:
- A computational microvascular model was developed using CE-MRI signal intensities from calf muscles.
- 56 participants (36 PAD patients, 20 controls) underwent CE-MRI and ankle-brachial index (ABI) testing at rest and after exercise.
- Key microvascular parameters (transfer rate constant, interstitial permeability, porosity, outflow filtration coefficient, microvascular pressure) were quantified and analyzed.
Main Results:
- Patients with PAD exhibited higher transfer rate constant, interstitial permeability, and microvascular pressure, with lower porosity and outflow filtration coefficient compared to controls (P≤0.014).
- All model parameters significantly correlated with ABI, claudication onset time, and peak walking time across all participants (P≤0.013).
- Within the PAD group, non-completers of treadmill exercise showed higher interstitial permeability and microvascular pressure, and lower porosity and outflow filtration coefficient than completers (P≤0.001).
Conclusions:
- Computational microvascular modeling parameters significantly differentiate PAD patients from controls.
- The model parameters are associated with clinical indicators of PAD severity and functional limitations.
- This computational approach holds potential for advancing the study of lower extremity ischemia and PAD.

