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(31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T

PURPOSE: To determine the phosphorus‐31 T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the healthy human brain at 7T. METHODS: A 3D chemical shift imaging multi‐echo sequence with composite block pulses for refocusing was used to measure one free induction decay (FID) and se...

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Autores principales: van der Kemp, Wybe J.M., Klomp, Dennis W.J., Wijnen, Jannie P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900879/
https://www.ncbi.nlm.nih.gov/pubmed/29215148
http://dx.doi.org/10.1002/mrm.27026
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author van der Kemp, Wybe J.M.
Klomp, Dennis W.J.
Wijnen, Jannie P.
author_facet van der Kemp, Wybe J.M.
Klomp, Dennis W.J.
Wijnen, Jannie P.
author_sort van der Kemp, Wybe J.M.
collection PubMed
description PURPOSE: To determine the phosphorus‐31 T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the healthy human brain at 7T. METHODS: A 3D chemical shift imaging multi‐echo sequence with composite block pulses for refocusing was used to measure one free induction decay (FID) and seven full echoes with an echo spacing of 45 ms on the brain of nine healthy volunteers (age range 22–45 years; average age 27 ± 8 years). Spectral fitting was used to determine the change in metabolic signal amplitude with echo time. RESULTS: The average apparent T(2)s with their standard deviation were 202 ± 6 ms, 129 ± 6 ms, 86 ± 2 ms, 214 ± 10 ms, and 213 ± 11 ms for phosphoethanolamine, phosphocholine, inorganic phosphate, glycerophosphoethanolamine, and glycerophosphocholine, respectively. CONCLUSION: The determined apparent T(2) for phosphoethanolamine, glycerophosphocholine, and glycerophosphoethanolamine is approximately 200 ms. The lower apparent T(2) value for phosphocholine is attributed to the overlap of this resonance with the 3‐phosphorous resonance of 2,3‐diphosphoglycerate from blood, with an apparent shorter T(2). Omitting the FID signal and the first echo of phosphocholine leads to a T(2) of 182 ± 7 ms, whereas a biexponential analysis leads to 203 ± 4 ms. These values are more in line with phosphoethanolamine and the phosphodiesters. The short T(2) of inorganic phosphate is subscribed to the fast reversible exchange with γ‐adenosine triphosphate, which is mediated by glyceraldehyde‐3‐phosphate dehydrogenase and phosphoglycerate kinase within the glycolytic pathway. Magn Reson Med 80:29–35, 2018. © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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spelling pubmed-59008792018-04-23 (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T van der Kemp, Wybe J.M. Klomp, Dennis W.J. Wijnen, Jannie P. Magn Reson Med Full Papers—Preclinical and Clinical Spectroscopy PURPOSE: To determine the phosphorus‐31 T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the healthy human brain at 7T. METHODS: A 3D chemical shift imaging multi‐echo sequence with composite block pulses for refocusing was used to measure one free induction decay (FID) and seven full echoes with an echo spacing of 45 ms on the brain of nine healthy volunteers (age range 22–45 years; average age 27 ± 8 years). Spectral fitting was used to determine the change in metabolic signal amplitude with echo time. RESULTS: The average apparent T(2)s with their standard deviation were 202 ± 6 ms, 129 ± 6 ms, 86 ± 2 ms, 214 ± 10 ms, and 213 ± 11 ms for phosphoethanolamine, phosphocholine, inorganic phosphate, glycerophosphoethanolamine, and glycerophosphocholine, respectively. CONCLUSION: The determined apparent T(2) for phosphoethanolamine, glycerophosphocholine, and glycerophosphoethanolamine is approximately 200 ms. The lower apparent T(2) value for phosphocholine is attributed to the overlap of this resonance with the 3‐phosphorous resonance of 2,3‐diphosphoglycerate from blood, with an apparent shorter T(2). Omitting the FID signal and the first echo of phosphocholine leads to a T(2) of 182 ± 7 ms, whereas a biexponential analysis leads to 203 ± 4 ms. These values are more in line with phosphoethanolamine and the phosphodiesters. The short T(2) of inorganic phosphate is subscribed to the fast reversible exchange with γ‐adenosine triphosphate, which is mediated by glyceraldehyde‐3‐phosphate dehydrogenase and phosphoglycerate kinase within the glycolytic pathway. Magn Reson Med 80:29–35, 2018. © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. John Wiley and Sons Inc. 2017-12-07 2018-07 /pmc/articles/PMC5900879/ /pubmed/29215148 http://dx.doi.org/10.1002/mrm.27026 Text en © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers—Preclinical and Clinical Spectroscopy
van der Kemp, Wybe J.M.
Klomp, Dennis W.J.
Wijnen, Jannie P.
(31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title_full (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title_fullStr (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title_full_unstemmed (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title_short (31)P T(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7T
title_sort (31)p t(2)s of phosphomonoesters, phosphodiesters, and inorganic phosphate in the human brain at 7t
topic Full Papers—Preclinical and Clinical Spectroscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900879/
https://www.ncbi.nlm.nih.gov/pubmed/29215148
http://dx.doi.org/10.1002/mrm.27026
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