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Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach
Metabolic markers of baseline brain oxygenation and tissue perfusion have an important role to play in the early identification of ischaemic tissue in acute stroke. Although well established MRI techniques exist for mapping brain perfusion, quantitative imaging of brain oxygenation is poorly served....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563088/ https://www.ncbi.nlm.nih.gov/pubmed/30860660 http://dx.doi.org/10.1002/hbm.24564 |
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author | Stone, Alan J. Harston, George W. J. Carone, Davide Okell, Thomas W. Kennedy, James Blockley, Nicholas P. |
author_facet | Stone, Alan J. Harston, George W. J. Carone, Davide Okell, Thomas W. Kennedy, James Blockley, Nicholas P. |
author_sort | Stone, Alan J. |
collection | PubMed |
description | Metabolic markers of baseline brain oxygenation and tissue perfusion have an important role to play in the early identification of ischaemic tissue in acute stroke. Although well established MRI techniques exist for mapping brain perfusion, quantitative imaging of brain oxygenation is poorly served. Streamlined‐qBOLD (sqBOLD) is a recently developed technique for mapping oxygenation that is well suited to the challenge of investigating acute stroke. In this study a noninvasive serial imaging protocol was implemented, incorporating sqBOLD and arterial spin labelling to map blood oxygenation and perfusion, respectively. The utility of these parameters was investigated using imaging based definitions of tissue outcome (ischaemic core, infarct growth and contralateral tissue). Voxel wise analysis revealed significant differences between all tissue outcomes using pairwise comparisons for the transverse reversible relaxation rate (R (2) ′), deoxygenated blood volume (DBV) and deoxyghaemoglobin concentration ([dHb]; p < 0.01 in all cases). At the patient level (n = 9), a significant difference was observed for [dHb] between ischaemic core and contralateral tissue. Furthermore, serial analysis at the patient level (n = 6) revealed significant changes in R (2) ′ between the presentation and 1 week scans for both ischaemic core (p < 0.01) and infarct growth (p < 0.05). In conclusion, this study presents evidence supporting the potential of sqBOLD for imaging oxygenation in stroke. |
format | Online Article Text |
id | pubmed-6563088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65630882019-06-17 Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach Stone, Alan J. Harston, George W. J. Carone, Davide Okell, Thomas W. Kennedy, James Blockley, Nicholas P. Hum Brain Mapp Research Articles Metabolic markers of baseline brain oxygenation and tissue perfusion have an important role to play in the early identification of ischaemic tissue in acute stroke. Although well established MRI techniques exist for mapping brain perfusion, quantitative imaging of brain oxygenation is poorly served. Streamlined‐qBOLD (sqBOLD) is a recently developed technique for mapping oxygenation that is well suited to the challenge of investigating acute stroke. In this study a noninvasive serial imaging protocol was implemented, incorporating sqBOLD and arterial spin labelling to map blood oxygenation and perfusion, respectively. The utility of these parameters was investigated using imaging based definitions of tissue outcome (ischaemic core, infarct growth and contralateral tissue). Voxel wise analysis revealed significant differences between all tissue outcomes using pairwise comparisons for the transverse reversible relaxation rate (R (2) ′), deoxygenated blood volume (DBV) and deoxyghaemoglobin concentration ([dHb]; p < 0.01 in all cases). At the patient level (n = 9), a significant difference was observed for [dHb] between ischaemic core and contralateral tissue. Furthermore, serial analysis at the patient level (n = 6) revealed significant changes in R (2) ′ between the presentation and 1 week scans for both ischaemic core (p < 0.01) and infarct growth (p < 0.05). In conclusion, this study presents evidence supporting the potential of sqBOLD for imaging oxygenation in stroke. John Wiley & Sons, Inc. 2019-03-12 /pmc/articles/PMC6563088/ /pubmed/30860660 http://dx.doi.org/10.1002/hbm.24564 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the 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 | Research Articles Stone, Alan J. Harston, George W. J. Carone, Davide Okell, Thomas W. Kennedy, James Blockley, Nicholas P. Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title | Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title_full | Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title_fullStr | Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title_full_unstemmed | Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title_short | Prospects for investigating brain oxygenation in acute stroke: Experience with a non‐contrast quantitative BOLD based approach |
title_sort | prospects for investigating brain oxygenation in acute stroke: experience with a non‐contrast quantitative bold based approach |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563088/ https://www.ncbi.nlm.nih.gov/pubmed/30860660 http://dx.doi.org/10.1002/hbm.24564 |
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