Foot Perfusion Measurements in Diabetic Patients with Pedal Ulcers Using Multimodal MRI

Author(s)
Edwards, Scott J.
Advisor(s)
Reiter, David A.
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Organizational Unit
Wallace H. Coulter Department of Biomedical Engineering
The joint Georgia Tech and Emory department was established in 1997
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Abstract
Hyperglycemia, a hallmark of uncontrolled type-2 diabetes mellitus (T2DM), is associated with several microvascular complications such as calcification of blood vessels, peripheral neuropathy, and slowed wound healing. In many cases, patients with T2DM will develop unresolved wounds on their feet called diabetic foot ulcers (DFUs), which are thought to occur in response to impaired microvascular function starving wound sites of critical nutrients and oxygen. The goal of this thesis is to examine the feasibility of using perfusion MRI to determine differences in perfusion in the feet of three age and body mass index matched groups: diabetic patients with foot ulcers (DFU, N=10), diabetic patients without DFUs and with controlled glycemia (DP, N=5) and healthy controls (HC, N=5). This thesis describes a pipeline to analyze the resting microvascular properties, characterized using intra-voxel incoherent motion imaging, and microvascular reactivity, characterized using blood-oxygenation level dependent imaging during a reactive hyperemia cuff- occlusion challenge, in feet with and without DFUs. We find that the DFU patients showed greater resting microvascular volume fraction (MVF) than DP patients (Hedge’s g MVF, MP = 1.46; g MVF, LP = 1.33), suggesting a hyperperfusion at rest. Additionally, the DFU patients also showed a greater ischemic reaction (g Min. Isch, LP = 1.50), and a blunted reperfusion reaction (g peak rep., MP = 2.37, g peak rep., LP = 1.22) compared to the DP during the cuff-occlusion challenge, suggesting a lowered ability for microvascular reactivity and arteriovenous shunting within the capillary beds. These findings suggest that parameters derived from multimodal MRI show a complimentary picture of underlying microvasculature dysfunction in patients with DFUs.
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Date
2023-05-02
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