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Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging

The original concept of the ischaemic penumbra suggested imaging of regional cerebral blood flow and metabolism would be required to identify tissue that may benefit from intervention. Amide proton transfer magnetic resonance imaging, a chemical exchange saturation transfer technique, has been used...

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Autores principales: Harston, George W. J., Tee, Yee Kai, Blockley, Nicholas, Okell, Thomas W., Thandeswaran, Sivarajan, Shaya, Gabriel, Sheerin, Fintan, Cellerini, Martino, Payne, Stephen, Jezzard, Peter, Chappell, Michael, Kennedy, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285197/
https://www.ncbi.nlm.nih.gov/pubmed/25564491
http://dx.doi.org/10.1093/brain/awu374
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author Harston, George W. J.
Tee, Yee Kai
Blockley, Nicholas
Okell, Thomas W.
Thandeswaran, Sivarajan
Shaya, Gabriel
Sheerin, Fintan
Cellerini, Martino
Payne, Stephen
Jezzard, Peter
Chappell, Michael
Kennedy, James
author_facet Harston, George W. J.
Tee, Yee Kai
Blockley, Nicholas
Okell, Thomas W.
Thandeswaran, Sivarajan
Shaya, Gabriel
Sheerin, Fintan
Cellerini, Martino
Payne, Stephen
Jezzard, Peter
Chappell, Michael
Kennedy, James
author_sort Harston, George W. J.
collection PubMed
description The original concept of the ischaemic penumbra suggested imaging of regional cerebral blood flow and metabolism would be required to identify tissue that may benefit from intervention. Amide proton transfer magnetic resonance imaging, a chemical exchange saturation transfer technique, has been used to derive cerebral intracellular pH in preclinical stroke models and has been proposed as a metabolic marker of ischaemic penumbra. In this proof of principle clinical study, we explored the potential of this pH-weighted magnetic resonance imaging technique at tissue-level. Detailed voxel-wise analysis was performed on data from a prospective cohort of 12 patients with acute ischaemic stroke. Voxels within ischaemic core had a more severe intracellular acidosis than hypoperfused tissue recruited to the final infarct (P < 0.0001), which in turn was more acidotic than hypoperfused tissue that survived (P < 0.0001). In addition, when confined to the grey matter perfusion deficit, intracellular pH (P < 0.0001), but not cerebral blood flow (P = 0.31), differed between tissue that infarcted and tissue that survived. Within the presenting apparent diffusion coefficient lesion, intracellular pH differed between tissue with early apparent diffusion lesion pseudonormalization and tissue with true radiographic recovery. These findings support the need for further investigation of pH-weighted imaging in patients with acute ischaemic stroke.
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spelling pubmed-42851972015-02-24 Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging Harston, George W. J. Tee, Yee Kai Blockley, Nicholas Okell, Thomas W. Thandeswaran, Sivarajan Shaya, Gabriel Sheerin, Fintan Cellerini, Martino Payne, Stephen Jezzard, Peter Chappell, Michael Kennedy, James Brain Reports The original concept of the ischaemic penumbra suggested imaging of regional cerebral blood flow and metabolism would be required to identify tissue that may benefit from intervention. Amide proton transfer magnetic resonance imaging, a chemical exchange saturation transfer technique, has been used to derive cerebral intracellular pH in preclinical stroke models and has been proposed as a metabolic marker of ischaemic penumbra. In this proof of principle clinical study, we explored the potential of this pH-weighted magnetic resonance imaging technique at tissue-level. Detailed voxel-wise analysis was performed on data from a prospective cohort of 12 patients with acute ischaemic stroke. Voxels within ischaemic core had a more severe intracellular acidosis than hypoperfused tissue recruited to the final infarct (P < 0.0001), which in turn was more acidotic than hypoperfused tissue that survived (P < 0.0001). In addition, when confined to the grey matter perfusion deficit, intracellular pH (P < 0.0001), but not cerebral blood flow (P = 0.31), differed between tissue that infarcted and tissue that survived. Within the presenting apparent diffusion coefficient lesion, intracellular pH differed between tissue with early apparent diffusion lesion pseudonormalization and tissue with true radiographic recovery. These findings support the need for further investigation of pH-weighted imaging in patients with acute ischaemic stroke. Oxford University Press 2015-01 2014-12-29 /pmc/articles/PMC4285197/ /pubmed/25564491 http://dx.doi.org/10.1093/brain/awu374 Text en © The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Reports
Harston, George W. J.
Tee, Yee Kai
Blockley, Nicholas
Okell, Thomas W.
Thandeswaran, Sivarajan
Shaya, Gabriel
Sheerin, Fintan
Cellerini, Martino
Payne, Stephen
Jezzard, Peter
Chappell, Michael
Kennedy, James
Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title_full Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title_fullStr Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title_full_unstemmed Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title_short Identifying the ischaemic penumbra using pH-weighted magnetic resonance imaging
title_sort identifying the ischaemic penumbra using ph-weighted magnetic resonance imaging
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285197/
https://www.ncbi.nlm.nih.gov/pubmed/25564491
http://dx.doi.org/10.1093/brain/awu374
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