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Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications

Dynamic susceptibility contrast (DSC) and arterial spin labeling (ASL) are techniques used to evaluate brain perfusion using MRI. DSC requires dynamic image acquisition with a rapid administration of gadolinium-based contrast agent. In contrast, ASL obtains brain perfusion information using magnetic...

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Autores principales: Kitajima, Mika, Uetani, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Magnetic Resonance in Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849418/
https://www.ncbi.nlm.nih.gov/pubmed/35321984
http://dx.doi.org/10.2463/mrms.rev.2021-0118
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author Kitajima, Mika
Uetani, Hiroyuki
author_facet Kitajima, Mika
Uetani, Hiroyuki
author_sort Kitajima, Mika
collection PubMed
description Dynamic susceptibility contrast (DSC) and arterial spin labeling (ASL) are techniques used to evaluate brain perfusion using MRI. DSC requires dynamic image acquisition with a rapid administration of gadolinium-based contrast agent. In contrast, ASL obtains brain perfusion information using magnetically labeled blood water as an endogenous tracer. For the evaluation of brain perfusion in pediatric neurological diseases, ASL has a significant advantage compared to DSC, CT, and single-photon emission CT/positron emission tomography because of the lack of radiation exposure and contrast agent administration. However, in ASL, optimization of several parameters, including the type of labeling, image acquisition, background suppression, and postlabeling delay, is required, because they have a significant effect on the quantification of cerebral blood flow (CBF). In this article, we first review recent technical developments of ASL and age-dependent physiological characteristics in pediatric brain perfusion. We then review the clinical implementation of ASL in pediatric neurological diseases, including vascular diseases, brain tumors, acute encephalopathy with biphasic seizure and late reduced diffusion (AESD), and migraine. In moyamoya disease, ASL can be used for brain perfusion and vessel assessment in pre- and post-treatment. In arteriovenous malformations, ASL is sensitive to detect small degrees of shunt. Furthermore, in vascular diseases, the implementation of ASL-based time-resolved MR angiography is described. In neoplasms, ASL-derived CBF has a high diagnostic accuracy for differentiation between low- and high-grade pediatric brain tumors. In AESD and migraine, ASL may allow for accurate early diagnosis and provide pathophysiological information.
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spelling pubmed-98494182023-01-26 Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications Kitajima, Mika Uetani, Hiroyuki Magn Reson Med Sci Review Dynamic susceptibility contrast (DSC) and arterial spin labeling (ASL) are techniques used to evaluate brain perfusion using MRI. DSC requires dynamic image acquisition with a rapid administration of gadolinium-based contrast agent. In contrast, ASL obtains brain perfusion information using magnetically labeled blood water as an endogenous tracer. For the evaluation of brain perfusion in pediatric neurological diseases, ASL has a significant advantage compared to DSC, CT, and single-photon emission CT/positron emission tomography because of the lack of radiation exposure and contrast agent administration. However, in ASL, optimization of several parameters, including the type of labeling, image acquisition, background suppression, and postlabeling delay, is required, because they have a significant effect on the quantification of cerebral blood flow (CBF). In this article, we first review recent technical developments of ASL and age-dependent physiological characteristics in pediatric brain perfusion. We then review the clinical implementation of ASL in pediatric neurological diseases, including vascular diseases, brain tumors, acute encephalopathy with biphasic seizure and late reduced diffusion (AESD), and migraine. In moyamoya disease, ASL can be used for brain perfusion and vessel assessment in pre- and post-treatment. In arteriovenous malformations, ASL is sensitive to detect small degrees of shunt. Furthermore, in vascular diseases, the implementation of ASL-based time-resolved MR angiography is described. In neoplasms, ASL-derived CBF has a high diagnostic accuracy for differentiation between low- and high-grade pediatric brain tumors. In AESD and migraine, ASL may allow for accurate early diagnosis and provide pathophysiological information. Japanese Society for Magnetic Resonance in Medicine 2022-03-23 /pmc/articles/PMC9849418/ /pubmed/35321984 http://dx.doi.org/10.2463/mrms.rev.2021-0118 Text en ©2022 Japanese Society for Magnetic Resonance in Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
Kitajima, Mika
Uetani, Hiroyuki
Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title_full Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title_fullStr Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title_full_unstemmed Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title_short Arterial Spin Labeling for Pediatric Central Nervous System Diseases: Techniques and Clinical Applications
title_sort arterial spin labeling for pediatric central nervous system diseases: techniques and clinical applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849418/
https://www.ncbi.nlm.nih.gov/pubmed/35321984
http://dx.doi.org/10.2463/mrms.rev.2021-0118
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