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Abstract #3290

Compartmentalised reconstruction of cardiac 31P concentric ring MRSI at 7T

Ferenc Emil Mozes1, Andrew Tyler2, Jack J. J. J. Miller1,3, William T. Clarke4, and Ladislav Valkovič1,5
1OCMR, RDM Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom, 2School of Biomedical Engineering and Imaging Sciences, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom, 3The MR Research Centre and the PET Centre, Aarhus University, Aarhus, Denmark, 4Wellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom, 5Department of Imaging Methods, Institute of Measurement Science, Slovak Academy of Sciences, Bratislava, Slovakia

Synopsis

Keywords: New Trajectories & Spatial Encoding Methods, Spectroscopy, Ultra high field

Motivation: Cardiac 31P MRS allows the probing of metabolism in various heart diseases, however, commonly employed 3D MRSI techniques are slow even at 7 T.

Goal(s): Our work aims to evaluate the use of compartment-based localised spectroscopy using a linear algebraic model (SLAM).

Approach: 31P MRSI data was collected using concentric ring trajectory acquisitions and SLAM was used to reconstruct 31P signal from the myocardium.

Results: We show increased SNR and reduced uncertainty in determining the cardiac PCr signal, in addition to also reducing the repeatability of PCr/ATP ratio measurements when compared to a 2.5 minute, NUFFT-reconstructed CRT protocol.

Impact: Repeatable and high-SNR 31P acquisitions will allow the probing of cardiac energetics in patient populations that were previously unable to attend prolonged scan sessions at ultra-high field strengths.

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