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Abstract #1892

Investigating metabolite regional dependencies in the frontal lobe: overlapping small and large voxels

Marilena M DeMayo1,2,3,4,5, Alexander McGirr2,3,4, Ben Selby3,6, Frank MacMaster7, Chantel T Debert3,6, and Ashley D Harris1,3,5
1Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada, 2Department of Psychiatry, University of Calgary, Calgary, AB, Canada, 3Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada, 4Mathison Centre for Mental Health Research and Education, University of Calgary, Calgary, AB, Canada, 5Department of Radiology, University of Calgary, Calgary, AB, Canada, 6Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada, 7Provincial Addiction and Mental Health (PAMH) Portfolio, University of Calgary, Calgary, AB, Canada

Synopsis

Small anatomically specific voxels in cerebral cortex require a large number of averages to quantify metabolites by magnetic resonance spectroscopy. It is unclear whether cortical regional variability in metabolite concentration requires small voxels, or whether a larger voxel which incorporates the region of interest can provide adequately representative measures with fewer averages. Concentrations of glutamate, glx, creatine, choline, myo­-inositol and N-acetyl-aspartate (NAA) were correlated within subjects between an overlapping small (15x15x15mm) and large (30x30x30mm) voxel. There was a significant correlation between creatine measures, while choline showed a positive trend. There was no correlation between glutamate, glx, NAA, and myo-inositol.

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Keywords