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Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T
PURPOSE: To assess reproducibility of glutamate measurement in the human brain by two short echo time (TE) (1)H-MRS sequences [stimulated echo acquisition mode (STEAM) and semi-localized by adiabatic selective refocusing (sLASER)] at 7 T. Reliable assessment of glutamate is important when studying a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399075/ https://www.ncbi.nlm.nih.gov/pubmed/28484398 http://dx.doi.org/10.3389/fpsyt.2017.00060 |
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author | Marsman, Anouk Boer, Vincent O. Luijten, Peter R. Hulshoff Pol, Hilleke E. Klomp, Dennis W. J. Mandl, René C. W. |
author_facet | Marsman, Anouk Boer, Vincent O. Luijten, Peter R. Hulshoff Pol, Hilleke E. Klomp, Dennis W. J. Mandl, René C. W. |
author_sort | Marsman, Anouk |
collection | PubMed |
description | PURPOSE: To assess reproducibility of glutamate measurement in the human brain by two short echo time (TE) (1)H-MRS sequences [stimulated echo acquisition mode (STEAM) and semi-localized by adiabatic selective refocusing (sLASER)] at 7 T. Reliable assessment of glutamate is important when studying a variety of neurological and neuropsychiatric disorders. At 7 T, the glutamate signal can be separated from the glutamine signal and hence more accurately measured as compared to lower field strengths. A sLASER sequence has been developed for 7 T, using field focusing at short TE, resulting in twice as much signal as can be obtained using STEAM and improved localization accuracy due to a decreased chemical shift artifact. MATERIALS AND METHODS: Eight subjects were scanned twice using both STEAM and sLASER. Data were acquired from the frontal and occipital brain region. Subsequently, intraclass correlations were computed for the estimated metabolite concentrations. RESULTS: sLASER has higher ICC’s for glutamate concentration as compared to STEAM in both the frontal and occipital VOI, which is probably due to the higher sensitivity and localization accuracy. CONCLUSION: We conclude that sLASER (1)H-MRS at 7 T is a reliable method to obtain reproducible measures of glutamate levels in the human brain at such high accuracy that individual variability, even between age-matched subjects, is measured. |
format | Online Article Text |
id | pubmed-5399075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53990752017-05-08 Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T Marsman, Anouk Boer, Vincent O. Luijten, Peter R. Hulshoff Pol, Hilleke E. Klomp, Dennis W. J. Mandl, René C. W. Front Psychiatry Psychiatry PURPOSE: To assess reproducibility of glutamate measurement in the human brain by two short echo time (TE) (1)H-MRS sequences [stimulated echo acquisition mode (STEAM) and semi-localized by adiabatic selective refocusing (sLASER)] at 7 T. Reliable assessment of glutamate is important when studying a variety of neurological and neuropsychiatric disorders. At 7 T, the glutamate signal can be separated from the glutamine signal and hence more accurately measured as compared to lower field strengths. A sLASER sequence has been developed for 7 T, using field focusing at short TE, resulting in twice as much signal as can be obtained using STEAM and improved localization accuracy due to a decreased chemical shift artifact. MATERIALS AND METHODS: Eight subjects were scanned twice using both STEAM and sLASER. Data were acquired from the frontal and occipital brain region. Subsequently, intraclass correlations were computed for the estimated metabolite concentrations. RESULTS: sLASER has higher ICC’s for glutamate concentration as compared to STEAM in both the frontal and occipital VOI, which is probably due to the higher sensitivity and localization accuracy. CONCLUSION: We conclude that sLASER (1)H-MRS at 7 T is a reliable method to obtain reproducible measures of glutamate levels in the human brain at such high accuracy that individual variability, even between age-matched subjects, is measured. Frontiers Media S.A. 2017-04-21 /pmc/articles/PMC5399075/ /pubmed/28484398 http://dx.doi.org/10.3389/fpsyt.2017.00060 Text en Copyright © 2017 Marsman, Boer, Luijten, Hulshoff Pol, Klomp and Mandl. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Marsman, Anouk Boer, Vincent O. Luijten, Peter R. Hulshoff Pol, Hilleke E. Klomp, Dennis W. J. Mandl, René C. W. Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title | Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title_full | Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title_fullStr | Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title_full_unstemmed | Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title_short | Detection of Glutamate Alterations in the Human Brain Using (1)H-MRS: Comparison of STEAM and sLASER at 7 T |
title_sort | detection of glutamate alterations in the human brain using (1)h-mrs: comparison of steam and slaser at 7 t |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399075/ https://www.ncbi.nlm.nih.gov/pubmed/28484398 http://dx.doi.org/10.3389/fpsyt.2017.00060 |
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