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Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla
PURPOSE: Cerebral blood flow (CBF) is an informative physiological marker for tissue health. Arterial spin labeling (ASL) is a noninvasive MRI method of measuring this parameter, but it has proven difficult to measure white matter (WM) CBF due to low intrinsic contrast-to-noise ratio compared with g...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657501/ https://www.ncbi.nlm.nih.gov/pubmed/24954898 http://dx.doi.org/10.1002/mrm.25333 |
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author | Gardener, Alexander G Jezzard, Peter |
author_facet | Gardener, Alexander G Jezzard, Peter |
author_sort | Gardener, Alexander G |
collection | PubMed |
description | PURPOSE: Cerebral blood flow (CBF) is an informative physiological marker for tissue health. Arterial spin labeling (ASL) is a noninvasive MRI method of measuring this parameter, but it has proven difficult to measure white matter (WM) CBF due to low intrinsic contrast-to-noise ratio compared with gray matter (GM). Here we combine ultra-high field and optimal sampling strategy (OSS) ASL to investigate WM CBF in reasonable scan times. METHODS: A FAIR-based ASL sequence at 7T was combined with a real-time-feedback OSS technique, to iteratively improve post-label image acquisition times (TIs) on a tissue- and subject-specific basis to obtain WM CBF quantification. RESULTS: It was found 77% of WM voxels gave a reasonable CBF fit. Averaged WM CBF for these voxels was found to be 16.3 ± 1.5 mL/100 g/min (discarding partial-volumed voxels). The generated TI schedule was also significantly different when altering the OSS weighted-tissue-mask, favoring longer TIs in WM. CONCLUSION: WM CBF could be reasonably quantified in over 75% of identified voxels, from a total preparation and scan time of 15 min. OSS results suggest longer TIs should be used versus general GM ASL settings; this may become more important in WM disease studies. Magn Reson Med 73:2243–2248, 2015. © 2014 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-4657501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46575012015-12-02 Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla Gardener, Alexander G Jezzard, Peter Magn Reson Med Imaging Methodology–Notes PURPOSE: Cerebral blood flow (CBF) is an informative physiological marker for tissue health. Arterial spin labeling (ASL) is a noninvasive MRI method of measuring this parameter, but it has proven difficult to measure white matter (WM) CBF due to low intrinsic contrast-to-noise ratio compared with gray matter (GM). Here we combine ultra-high field and optimal sampling strategy (OSS) ASL to investigate WM CBF in reasonable scan times. METHODS: A FAIR-based ASL sequence at 7T was combined with a real-time-feedback OSS technique, to iteratively improve post-label image acquisition times (TIs) on a tissue- and subject-specific basis to obtain WM CBF quantification. RESULTS: It was found 77% of WM voxels gave a reasonable CBF fit. Averaged WM CBF for these voxels was found to be 16.3 ± 1.5 mL/100 g/min (discarding partial-volumed voxels). The generated TI schedule was also significantly different when altering the OSS weighted-tissue-mask, favoring longer TIs in WM. CONCLUSION: WM CBF could be reasonably quantified in over 75% of identified voxels, from a total preparation and scan time of 15 min. OSS results suggest longer TIs should be used versus general GM ASL settings; this may become more important in WM disease studies. Magn Reson Med 73:2243–2248, 2015. © 2014 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 & Sons, Ltd 2015-06 2014-06-20 /pmc/articles/PMC4657501/ /pubmed/24954898 http://dx.doi.org/10.1002/mrm.25333 Text en © 2014 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Imaging Methodology–Notes Gardener, Alexander G Jezzard, Peter Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title | Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title_full | Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title_fullStr | Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title_full_unstemmed | Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title_short | Investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 Tesla |
title_sort | investigating white matter perfusion using optimal sampling strategy arterial spin labeling at 7 tesla |
topic | Imaging Methodology–Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657501/ https://www.ncbi.nlm.nih.gov/pubmed/24954898 http://dx.doi.org/10.1002/mrm.25333 |
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