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Abstract #0894

Creatine CH2 and PCr dynamics closely correlate in dynamic interleaved MRS of exercising muscle

Radka Klepochova1,2, Fabian Niess2, Siegfried Trattnig2,3,4,5, Alexandra Kautzky-Willer1, Martin Krššák1,2, and Martin Meyerspeer6
1Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria, 2High-Field MR Center, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria, 3CD Laboratory for MR Imaging Biomarkers (BIOMAK), Vienna, Austria, 4Austrian Cluster for Tissue Regeneration, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria, 5Institute for Clinical Molecular MRI in the Musculoskeletal System, Karl Landsteiner Society, Vienna, Austria, 6High-Field MR Center, Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria

Synopsis

Keywords: Muscle, Spectroscopy

Motivation: To explore quantification of skeletal muscle oxidative metabolism by 1H MRS.

Goal(s): We used the increased accuracy of 7T MRS with a dedicated RF-coil, interleaved acquisition and localization of 31P information to compare Creatine-CH2 and Phosphocreatine time courses during exercise and recovery.

Approach: Eight volunteers were measured on a 7T MR system with RF-coil and ergometer dedicated for exercise. 1H and 31P MR spectra were acquired interleaved during exercise and recovery.

Results: Exercise led to disappearance of the Creatine-CH2 resonance, while the CH3 resonance remained stable during exercise. The recovery time constants were similar (τPCr=37±9s and τCr=34±6s) and positively correlated.

Impact: The time course of the Creatine-CH2 resonance in skeletal muscle can be accessed via dynamic 1H MRS. If accurately reflecting oxidative metabolism, this technique has the potential to render non-invasive metabolic studies broadly accessible, without needing multi-nuclear MRI capabilities.

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