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Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla
PURPOSE: Phosphorus ((31)P) metabolites are emerging liver disease biomarkers. Of particular interest are phosphomonoester and phosphodiester (PDE) “peaks” that comprise multiple overlapping resonances in (31)P spectra. This study investigates the effect of improved spectral resolution at 7 Tesla (T...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697655/ https://www.ncbi.nlm.nih.gov/pubmed/28244131 http://dx.doi.org/10.1002/mrm.26635 |
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author | Purvis, Lucian A.B. Clarke, William T. Valkovič, Ladislav Levick, Christina Pavlides, Michael Barnes, Eleanor Cobbold, Jeremy F. Robson, Matthew D. Rodgers, Christopher T. |
author_facet | Purvis, Lucian A.B. Clarke, William T. Valkovič, Ladislav Levick, Christina Pavlides, Michael Barnes, Eleanor Cobbold, Jeremy F. Robson, Matthew D. Rodgers, Christopher T. |
author_sort | Purvis, Lucian A.B. |
collection | PubMed |
description | PURPOSE: Phosphorus ((31)P) metabolites are emerging liver disease biomarkers. Of particular interest are phosphomonoester and phosphodiester (PDE) “peaks” that comprise multiple overlapping resonances in (31)P spectra. This study investigates the effect of improved spectral resolution at 7 Tesla (T) on quantifying hepatic metabolites in cirrhosis. METHODS: Five volunteers were scanned to determine metabolite T(1)s. Ten volunteers and 11 patients with liver cirrhosis were scanned at 7T. Liver spectra were acquired in 28 min using a 16‐channel (31)P array and 3D chemical shift imaging. Concentrations were calculated using γ‐adenosine‐triphosphate (γ‐ATP) = 2.65 mmol/L wet tissue. RESULTS: T(1) means ± standard deviations: phosphatidylcholine 1.05 ± 0.28 s, nicotinamide‐adenine‐dinucleotide (NAD(+)) 2.0 ± 1.0 s, uridine‐diphosphoglucose (UDPG) 3.3 ± 1.4 s. Concentrations in healthy volunteers: α‐ATP 2.74 ± 0.11 mmol/L wet tissue, inorganic phosphate 2.23 ± 0.20 mmol/L wet tissue, glycerophosphocholine 2.34 ± 0.46 mmol/L wet tissue, glycerophosphoethanolamine 1.50 ± 0.28 mmol/L wet tissue, phosphocholine 1.06 ± 0.16 mmol/L wet tissue, phosphoethanolamine 0.77 ± 0.14 mmol/L wet tissue, NAD(+) 2.37 ± 0.14 mmol/L wet tissue, UDPG 2.00 ± 0.22 mmol/L wet tissue, phosphatidylcholine 1.38 ± 0.31 mmol/L wet tissue. Inorganic phosphate and phosphatidylcholine concentrations were significantly lower in patients; glycerophosphoethanolamine concentrations were significantly higher (P < 0.05). CONCLUSION: We report human in vivo hepatic T(1)s for phosphatidylcholine, NAD(+), and UDPG for the first time at 7T. Our protocol allows high signal‐to‐noise, repeatable measurement of metabolite concentrations in human liver. The splitting of PDE into its constituent peaks at 7T may allow more insight into changes in metabolism. Magn Reson Med 78:2095–2105, 2017. © 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 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
format | Online Article Text |
id | pubmed-5697655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56976552017-11-28 Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla Purvis, Lucian A.B. Clarke, William T. Valkovič, Ladislav Levick, Christina Pavlides, Michael Barnes, Eleanor Cobbold, Jeremy F. Robson, Matthew D. Rodgers, Christopher T. Magn Reson Med Full Papers—Spectroscopic Methodology PURPOSE: Phosphorus ((31)P) metabolites are emerging liver disease biomarkers. Of particular interest are phosphomonoester and phosphodiester (PDE) “peaks” that comprise multiple overlapping resonances in (31)P spectra. This study investigates the effect of improved spectral resolution at 7 Tesla (T) on quantifying hepatic metabolites in cirrhosis. METHODS: Five volunteers were scanned to determine metabolite T(1)s. Ten volunteers and 11 patients with liver cirrhosis were scanned at 7T. Liver spectra were acquired in 28 min using a 16‐channel (31)P array and 3D chemical shift imaging. Concentrations were calculated using γ‐adenosine‐triphosphate (γ‐ATP) = 2.65 mmol/L wet tissue. RESULTS: T(1) means ± standard deviations: phosphatidylcholine 1.05 ± 0.28 s, nicotinamide‐adenine‐dinucleotide (NAD(+)) 2.0 ± 1.0 s, uridine‐diphosphoglucose (UDPG) 3.3 ± 1.4 s. Concentrations in healthy volunteers: α‐ATP 2.74 ± 0.11 mmol/L wet tissue, inorganic phosphate 2.23 ± 0.20 mmol/L wet tissue, glycerophosphocholine 2.34 ± 0.46 mmol/L wet tissue, glycerophosphoethanolamine 1.50 ± 0.28 mmol/L wet tissue, phosphocholine 1.06 ± 0.16 mmol/L wet tissue, phosphoethanolamine 0.77 ± 0.14 mmol/L wet tissue, NAD(+) 2.37 ± 0.14 mmol/L wet tissue, UDPG 2.00 ± 0.22 mmol/L wet tissue, phosphatidylcholine 1.38 ± 0.31 mmol/L wet tissue. Inorganic phosphate and phosphatidylcholine concentrations were significantly lower in patients; glycerophosphoethanolamine concentrations were significantly higher (P < 0.05). CONCLUSION: We report human in vivo hepatic T(1)s for phosphatidylcholine, NAD(+), and UDPG for the first time at 7T. Our protocol allows high signal‐to‐noise, repeatable measurement of metabolite concentrations in human liver. The splitting of PDE into its constituent peaks at 7T may allow more insight into changes in metabolism. Magn Reson Med 78:2095–2105, 2017. © 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 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. John Wiley and Sons Inc. 2017-02-28 2017-12 /pmc/articles/PMC5697655/ /pubmed/28244131 http://dx.doi.org/10.1002/mrm.26635 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 Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers—Spectroscopic Methodology Purvis, Lucian A.B. Clarke, William T. Valkovič, Ladislav Levick, Christina Pavlides, Michael Barnes, Eleanor Cobbold, Jeremy F. Robson, Matthew D. Rodgers, Christopher T. Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title | Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title_full | Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title_fullStr | Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title_full_unstemmed | Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title_short | Phosphodiester content measured in human liver by in vivo (31)P MR spectroscopy at 7 tesla |
title_sort | phosphodiester content measured in human liver by in vivo (31)p mr spectroscopy at 7 tesla |
topic | Full Papers—Spectroscopic Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697655/ https://www.ncbi.nlm.nih.gov/pubmed/28244131 http://dx.doi.org/10.1002/mrm.26635 |
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