NMR in Biomedicine, volume 35, issue 2
Reproducibility of 7‐T brain spectroscopy using an ultrashort echo time STimulated Echo Acquisition Mode sequence and automated voxel repositioning
Meredith A. Reid
1, 2
,
Martha R. Forloines
3
,
Nouha Salibi
4
2
Alabama Advanced Imaging Consortium Auburn Alabama USA
|
4
MR R&D Siemens Healthineers Malvern PA USA
|
Publication type: Journal Article
Publication date: 2021-10-08
Journal:
NMR in Biomedicine
scimago Q1
SJR: 0.949
CiteScore: 6.0
Impact factor: 2.7
ISSN: 09523480, 10991492
DOI:
10.1002/nbm.4631
PubMed ID:
34622996
Spectroscopy
Molecular Medicine
Radiology, Nuclear Medicine and imaging
Abstract
Establishing the reproducibility of brain MRS is important for clinical studies so that researchers can evaluate changes in metabolites due to treatment or the course of a disease and better understand the brain in healthy and disordered states. Prior 7-T MRS reproducibility studies using the stimulated echo acquisition mode (STEAM) sequence have focused on the anterior cingulate cortex or posterior cingulate cortex and precuneus. The purpose of this study was to evaluate the reproducibility of metabolite measurements in the dorsolateral prefrontal cortex (DLPFC) using an ultrashort echo time (TE) STEAM sequence and automated voxel repositioning. Spectra were acquired during two scan sessions from nine subjects using the AutoAlign method for voxel repositioning. Reproducibility was evaluated with coefficients of variation (CVs) and percentage differences. The mean intrasubject CVs were less than 6% for the major metabolites glutamate, N-acetylaspartate, total creatine, total choline, and myo-inositol. The mean CVs were less than 20% for the smaller signals of GABA, glutamine, glutathione, and taurine. These results indicate that 7-T MRS using a STEAM sequence with ultrashort TE and automated voxel repositioning provides excellent reproducibility of metabolites in the DLPFC.
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