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Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept
We present a feasibility study of sodium quantification in a multicompartment model of the brain using sodium ((23)Na) magnetic resonance imaging. The proposed method is based on a multipulse sequence acquisition and simulation at 7 T, which allows to differentiate the (23)Na signals emanating from...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727256/ https://www.ncbi.nlm.nih.gov/pubmed/29234043 http://dx.doi.org/10.1038/s41598-017-17582-w |
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author | Gilles, Alina Nagel, Armin M. Madelin, Guillaume |
author_facet | Gilles, Alina Nagel, Armin M. Madelin, Guillaume |
author_sort | Gilles, Alina |
collection | PubMed |
description | We present a feasibility study of sodium quantification in a multicompartment model of the brain using sodium ((23)Na) magnetic resonance imaging. The proposed method is based on a multipulse sequence acquisition and simulation at 7 T, which allows to differentiate the (23)Na signals emanating from three compartments in human brain in vivo: intracellular (compartment 1), extracellular (compartment 2), and cerebrospinal fluid (compartment 3). The intracellular sodium concentration C (1) and the volume fractions α (1), α (2), and α (3) of all respective three brain compartments can be estimated. Simulations of the sodium spin 3/2 dynamics during a 15-pulse sequence were used to optimize the acquisition sequence by minimizing the correlation between the signal evolutions from the three compartments. The method was first tested on a three-compartment phantom as proof-of-concept. Average values of the (23)Na quantifications in four healthy volunteer brains were α (1) = 0.54 ± 0.01, α (2) = 0.23 ± 0.01, α (3) = 1.03 ± 0.01, and C (1) = 23 ± 3 mM, which are comparable to the expected physiological values [Formula: see text] ∼ 0.6, [Formula: see text] ∼ 0.2, [Formula: see text] ∼ 1, and [Formula: see text] ∼ 10–30 mM. The proposed method may allow a quantitative assessment of the metabolic role of sodium ions in cellular processes and their malfunctions in brain in vivo. |
format | Online Article Text |
id | pubmed-5727256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57272562017-12-13 Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept Gilles, Alina Nagel, Armin M. Madelin, Guillaume Sci Rep Article We present a feasibility study of sodium quantification in a multicompartment model of the brain using sodium ((23)Na) magnetic resonance imaging. The proposed method is based on a multipulse sequence acquisition and simulation at 7 T, which allows to differentiate the (23)Na signals emanating from three compartments in human brain in vivo: intracellular (compartment 1), extracellular (compartment 2), and cerebrospinal fluid (compartment 3). The intracellular sodium concentration C (1) and the volume fractions α (1), α (2), and α (3) of all respective three brain compartments can be estimated. Simulations of the sodium spin 3/2 dynamics during a 15-pulse sequence were used to optimize the acquisition sequence by minimizing the correlation between the signal evolutions from the three compartments. The method was first tested on a three-compartment phantom as proof-of-concept. Average values of the (23)Na quantifications in four healthy volunteer brains were α (1) = 0.54 ± 0.01, α (2) = 0.23 ± 0.01, α (3) = 1.03 ± 0.01, and C (1) = 23 ± 3 mM, which are comparable to the expected physiological values [Formula: see text] ∼ 0.6, [Formula: see text] ∼ 0.2, [Formula: see text] ∼ 1, and [Formula: see text] ∼ 10–30 mM. The proposed method may allow a quantitative assessment of the metabolic role of sodium ions in cellular processes and their malfunctions in brain in vivo. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727256/ /pubmed/29234043 http://dx.doi.org/10.1038/s41598-017-17582-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gilles, Alina Nagel, Armin M. Madelin, Guillaume Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title | Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title_full | Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title_fullStr | Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title_full_unstemmed | Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title_short | Multipulse sodium magnetic resonance imaging for multicompartment quantification: Proof-of-concept |
title_sort | multipulse sodium magnetic resonance imaging for multicompartment quantification: proof-of-concept |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727256/ https://www.ncbi.nlm.nih.gov/pubmed/29234043 http://dx.doi.org/10.1038/s41598-017-17582-w |
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