1371-P: Dynamic Mapping of Skeletal Muscle Perfusion and Phosphocreatine with 1H Magnetic Resonance Imaging: A Rest-Exercise Study in Diabetes

Aim: Evaluating time and spatially resolved 1H magnetic resonance imaging (MRI) in quantifying muscle tissue phosphocreatine (PCr) kinetics (without extra hardware) and perfusion in healthy individuals and patients with type 2 diabetes mellitus (DM) . Methods: 18 subjects were imaged in 3 groups usi...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2022-06, Vol.71 (Supplement_1)
Hauptverfasser: WAHIDI, RYAN, LI, RAN, ZAYED, MOHAMED A., HASTINGS, MARY, ZHENG, JIE
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Sprache:eng
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Zusammenfassung:Aim: Evaluating time and spatially resolved 1H magnetic resonance imaging (MRI) in quantifying muscle tissue phosphocreatine (PCr) kinetics (without extra hardware) and perfusion in healthy individuals and patients with type 2 diabetes mellitus (DM) . Methods: 18 subjects were imaged in 3 groups using a 3T MRI scanner; young healthy (26y, n= 6) , old healthy (62y, n = 6) , and DM patients (66y, n = 6) . For each subject, a chemical exchange saturation transfer (CEST) MRI scan was performed in the calf every 1 min at rest (3 min) , during exercise (4 min standardized isometric plantarflexion) , and a recovery period (6 min) . Subjects also underwent mapping of skeletal muscle perfusion in a separate exercise protocol. PCr concentration maps were quantified by Bloch-McConnell fitting, and values were obtained in the medial gastrocnemius and soleus muscles. Results: DM patients show a longer PCr recovery time τ during recovery compared to both healthy groups: young healthy τ = 47.1 ± 18.2s, old healthy τ = 41.9 ± 15.1s, and DM τ =122.2 ± 58.6s, p = 0.02 (Figure) . There is a negative correlation between PCr and perfusion during exercise in healthy groups (r = 0.38, p = 0.034) that is not significant in the DM group. Conclusion: Dynamic PCr mapping by proton MRI in calf muscle reveals impaired energetics that is uncoupled from muscle perfusion in DM compared to healthy controls.
ISSN:0012-1797
1939-327X
DOI:10.2337/db22-1371-P