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Comparison of human brain metabolite levels using 1H MRS at 1.5T and 3.0T
Proton magnetic resonance spectroscopy (MRS) of the human brain has proven to be a useful technique in several neurological and psychiatric disorders and benefits from higher field scanners as signal intensity and spectral resolution are proportional to the magnetic field strength. OBJECTIVE: To inv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Neurologia Cognitiva e do
Comportamento
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619521/ https://www.ncbi.nlm.nih.gov/pubmed/29213843 http://dx.doi.org/10.1590/S1980-57642013DN70200013 |
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author | Paiva, Fernando Fernandes Otaduy, Maria Concepcion Garcia de Oliveira-Souza, Ricardo Moll, Jorge Bramati, Ivanei Edson Oliveira, Luciane de Souza, Andrea Silveira Tovar-Moll, Fernanda |
author_facet | Paiva, Fernando Fernandes Otaduy, Maria Concepcion Garcia de Oliveira-Souza, Ricardo Moll, Jorge Bramati, Ivanei Edson Oliveira, Luciane de Souza, Andrea Silveira Tovar-Moll, Fernanda |
author_sort | Paiva, Fernando Fernandes |
collection | PubMed |
description | Proton magnetic resonance spectroscopy (MRS) of the human brain has proven to be a useful technique in several neurological and psychiatric disorders and benefits from higher field scanners as signal intensity and spectral resolution are proportional to the magnetic field strength. OBJECTIVE: To investigate the effects of the magnetic field on the measurement of brain metabolites in a typical routine clinical setting. METHODS: Single voxel spectra were acquired from the posterior cingulate cortex in 26 healthy subjects. Each subject was scanned consecutively at 1.5T and 3.0T in a randomly distributed order. RESULTS: SNR and peak width improvements were observed at higher fields. However, SNR improvement was lower than the theoretical two-fold improvement. Other than the values obtained for creatine (Cre) and myo-Inositol (mI), which were both higher at 3.0T, all metabolite concentrations obtained were roughly the same at both field strengths. All the metabolite concentrations were estimated with a Cramer Rao lower bounds (CRLB) lower than 15% of the calculated concentrations. CONCLUSIONS: Even though the present study supports the expected benefits of higher field strength for MRS, there are several factors that can lead to different quantitative results when comparing 1.5T to 3.0T MRS. Future comparative studies are necessary to refine the metabolite thresholds for early detection and quantification of distinct neurological and psychiatric disorders using 3.0T MRS. |
format | Online Article Text |
id | pubmed-5619521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Associação de Neurologia Cognitiva e do
Comportamento |
record_format | MEDLINE/PubMed |
spelling | pubmed-56195212017-12-06 Comparison of human brain metabolite levels using 1H MRS at 1.5T and 3.0T Paiva, Fernando Fernandes Otaduy, Maria Concepcion Garcia de Oliveira-Souza, Ricardo Moll, Jorge Bramati, Ivanei Edson Oliveira, Luciane de Souza, Andrea Silveira Tovar-Moll, Fernanda Dement Neuropsychol Original Articles Proton magnetic resonance spectroscopy (MRS) of the human brain has proven to be a useful technique in several neurological and psychiatric disorders and benefits from higher field scanners as signal intensity and spectral resolution are proportional to the magnetic field strength. OBJECTIVE: To investigate the effects of the magnetic field on the measurement of brain metabolites in a typical routine clinical setting. METHODS: Single voxel spectra were acquired from the posterior cingulate cortex in 26 healthy subjects. Each subject was scanned consecutively at 1.5T and 3.0T in a randomly distributed order. RESULTS: SNR and peak width improvements were observed at higher fields. However, SNR improvement was lower than the theoretical two-fold improvement. Other than the values obtained for creatine (Cre) and myo-Inositol (mI), which were both higher at 3.0T, all metabolite concentrations obtained were roughly the same at both field strengths. All the metabolite concentrations were estimated with a Cramer Rao lower bounds (CRLB) lower than 15% of the calculated concentrations. CONCLUSIONS: Even though the present study supports the expected benefits of higher field strength for MRS, there are several factors that can lead to different quantitative results when comparing 1.5T to 3.0T MRS. Future comparative studies are necessary to refine the metabolite thresholds for early detection and quantification of distinct neurological and psychiatric disorders using 3.0T MRS. Associação de Neurologia Cognitiva e do Comportamento 2013 /pmc/articles/PMC5619521/ /pubmed/29213843 http://dx.doi.org/10.1590/S1980-57642013DN70200013 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Paiva, Fernando Fernandes Otaduy, Maria Concepcion Garcia de Oliveira-Souza, Ricardo Moll, Jorge Bramati, Ivanei Edson Oliveira, Luciane de Souza, Andrea Silveira Tovar-Moll, Fernanda Comparison of human brain metabolite levels using 1H MRS at 1.5T and 3.0T |
title | Comparison of human brain metabolite levels using 1H MRS at 1.5T and
3.0T |
title_full | Comparison of human brain metabolite levels using 1H MRS at 1.5T and
3.0T |
title_fullStr | Comparison of human brain metabolite levels using 1H MRS at 1.5T and
3.0T |
title_full_unstemmed | Comparison of human brain metabolite levels using 1H MRS at 1.5T and
3.0T |
title_short | Comparison of human brain metabolite levels using 1H MRS at 1.5T and
3.0T |
title_sort | comparison of human brain metabolite levels using 1h mrs at 1.5t and
3.0t |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619521/ https://www.ncbi.nlm.nih.gov/pubmed/29213843 http://dx.doi.org/10.1590/S1980-57642013DN70200013 |
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