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Abstract #2476

Calf muscle oxygen extraction fraction measurement using the multi contrast EPI with keyhole sequence – feasibility study.

Marzena Wylezinska-Arridge1,2, Chiara Pizzamiglio3, Fabian Küppers 4, N. Jon Shah4,5,6,7, Laura Mancini1,2, David Thomas2, Robert D.S. Pitceathly3,8, and John S Thornton1,2
1Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, London, United Kingdom, 2Neuroradiological Academic Unit, UCL Queen Square Institute of Neurology, London, United Kingdom, 3Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, United Kingdom, 4Institute of Neuroscience and Medicine 4, Forschungszentrum Jülich, Jülich, Germany, 5Institute of Neuroscience and Medicine 11, Forschungszentrum Jülich, Jülich, Germany, 6JARA_BRAIN -Translational Medicine, Aachen, Germany, 7Department of Neurology, RWTH Aachen University Hospital, Aachen, Germany, 8NHS Highly Specialised Service for Rare Mitochondrial Disorders, Queen Square Centre for Neuromuscular Diseases, National Hospital for Neurology and Neurosurgery, London, United Kingdom

Synopsis

Keywords: Oxygenation, Muscle, Oxygen metabolism in muscle

Motivation: Muscle Oxygen extraction fraction (OEF) may provide a potential biomarker of muscular disease.

Goal(s): The aim was to investigate application of a recently developed multi contrast EPI with keyhole sequence (GE-SE-EPIK) to quantify OEF in skeletal muscle.

Approach: Sequence was used to measure T2, T2* and OEF in healthy volunteers calf muscle at rest (to test reproducibility) and during a cuff compression (to test sensitivity to detect dynamic OEF changes).

Results: Values of T2, T2* and OEF measured at rest, correspond to those in literature. Sufficient reproducibility and sensitivity suggest suitability of GE-SE_EPIK for in vivo measurements for functional imaging of calf muscle.

Impact: This work supports the feasibility of using a recently developed multi contrast EPI with keyhole sequence to quantify T2, T2* and oxygen extraction fraction in skeletal muscle. This could prove a valuable tool for studying oxygen metabolism in muscles in health and disease.

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Keywords