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Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage

OBJECT: We studied the feasibility of pseudocontinuous arterial spin labeling (pCASL) at 7 T. MATERIALS AND METHODS: Simulations were performed to find the optimal labeling parameters for pCASL, with particular attention to the maximum-allowed specific absorption rate (SAR). Subsequently, pCASL expe...

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Autores principales: Ghariq, Eidrees, Teeuwisse, Wouter M., Webb, Andrew G., van Osch, Matthias J. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313026/
https://www.ncbi.nlm.nih.gov/pubmed/22200964
http://dx.doi.org/10.1007/s10334-011-0297-0
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author Ghariq, Eidrees
Teeuwisse, Wouter M.
Webb, Andrew G.
van Osch, Matthias J. P.
author_facet Ghariq, Eidrees
Teeuwisse, Wouter M.
Webb, Andrew G.
van Osch, Matthias J. P.
author_sort Ghariq, Eidrees
collection PubMed
description OBJECT: We studied the feasibility of pseudocontinuous arterial spin labeling (pCASL) at 7 T. MATERIALS AND METHODS: Simulations were performed to find the optimal labeling parameters for pCASL, with particular attention to the maximum-allowed specific absorption rate (SAR). Subsequently, pCASL experiments (four volunteers) were performed to find the B1 efficiency at the labeling position with and without high-permittivity pads placed around the head, and to study the optimal labeling duration (four separate volunteers). Finally, feasibility of whole-brain pCASL imaging was tested. RESULTS: Simulations showed that a lower B1 efficiency should be compensated by a lower effective flip angle of the labeling, a moderately shorter labeling duration, and a longer repetition time. B1 efficiency in the internal carotid arteries just below the carotid siphon was approximately 55% and 35% with and without high-permittivity pads, respectively. In vivo experiments showed an optimal labeling duration of 1,500 ms, although longer labeling durations up to 2,500 ms resulted in similar signal-to-noise efficiency. Whole-brain pCASL imaging was demonstrated in a single volunteer. CONCLUSION: Despite decreased B1 efficiency, sufficient labeling efficiency can be achieved for whole-brain pCASL at 7 T with high-permittivity pads. However, image quality is still limited compared with 3 T, probably due to imaging instabilities, and further research is needed to elucidate this.
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spelling pubmed-33130262012-03-30 Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage Ghariq, Eidrees Teeuwisse, Wouter M. Webb, Andrew G. van Osch, Matthias J. P. MAGMA Research Article OBJECT: We studied the feasibility of pseudocontinuous arterial spin labeling (pCASL) at 7 T. MATERIALS AND METHODS: Simulations were performed to find the optimal labeling parameters for pCASL, with particular attention to the maximum-allowed specific absorption rate (SAR). Subsequently, pCASL experiments (four volunteers) were performed to find the B1 efficiency at the labeling position with and without high-permittivity pads placed around the head, and to study the optimal labeling duration (four separate volunteers). Finally, feasibility of whole-brain pCASL imaging was tested. RESULTS: Simulations showed that a lower B1 efficiency should be compensated by a lower effective flip angle of the labeling, a moderately shorter labeling duration, and a longer repetition time. B1 efficiency in the internal carotid arteries just below the carotid siphon was approximately 55% and 35% with and without high-permittivity pads, respectively. In vivo experiments showed an optimal labeling duration of 1,500 ms, although longer labeling durations up to 2,500 ms resulted in similar signal-to-noise efficiency. Whole-brain pCASL imaging was demonstrated in a single volunteer. CONCLUSION: Despite decreased B1 efficiency, sufficient labeling efficiency can be achieved for whole-brain pCASL at 7 T with high-permittivity pads. However, image quality is still limited compared with 3 T, probably due to imaging instabilities, and further research is needed to elucidate this. Springer-Verlag 2011-12-27 2012 /pmc/articles/PMC3313026/ /pubmed/22200964 http://dx.doi.org/10.1007/s10334-011-0297-0 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Research Article
Ghariq, Eidrees
Teeuwisse, Wouter M.
Webb, Andrew G.
van Osch, Matthias J. P.
Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title_full Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title_fullStr Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title_full_unstemmed Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title_short Feasibility of pseudocontinuous arterial spin labeling at 7 T with whole-brain coverage
title_sort feasibility of pseudocontinuous arterial spin labeling at 7 t with whole-brain coverage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313026/
https://www.ncbi.nlm.nih.gov/pubmed/22200964
http://dx.doi.org/10.1007/s10334-011-0297-0
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