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Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI

Introduction: Cerebral blood flow (CBF) is an important physiological parameter that can be quantified non-invasively using arterial spin labelling (ASL) imaging. Although most ASL studies are based on single-timepoint strategies, multi-timepoint approaches (multiple-PLD) in combination with appropr...

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Autores principales: Pinto, Joana, Blockley, Nicholas P., Harkin, James W., Bulte, Daniel P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250662/
https://www.ncbi.nlm.nih.gov/pubmed/37304817
http://dx.doi.org/10.3389/fphys.2023.1142359
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author Pinto, Joana
Blockley, Nicholas P.
Harkin, James W.
Bulte, Daniel P.
author_facet Pinto, Joana
Blockley, Nicholas P.
Harkin, James W.
Bulte, Daniel P.
author_sort Pinto, Joana
collection PubMed
description Introduction: Cerebral blood flow (CBF) is an important physiological parameter that can be quantified non-invasively using arterial spin labelling (ASL) imaging. Although most ASL studies are based on single-timepoint strategies, multi-timepoint approaches (multiple-PLD) in combination with appropriate model fitting strategies may be beneficial not only to improve CBF quantification but also to retrieve other physiological information of interest. Methods: In this work, we tested several kinetic models for the fitting of multiple-PLD pCASL data in a group of 10 healthy subjects. In particular, we extended the standard kinetic model by incorporating dispersion effects and the macrovascular contribution and assessed their individual and combined effect on CBF quantification. These assessments were performed using two pseudo-continuous ASL (pCASL) datasets acquired in the same subjects but during two conditions mimicking different CBF dynamics: normocapnia and hypercapnia (achieved through a CO(2) stimulus). Results: All kinetic models quantified and highlighted the different CBF spatiotemporal dynamics between the two conditions. Hypercapnia led to an increase in CBF whilst decreasing arterial transit time (ATT) and arterial blood volume (aBV). When comparing the different kinetic models, the incorporation of dispersion effects yielded a significant decrease in CBF (∼10–22%) and ATT (∼17–26%), whilst aBV (∼44–74%) increased, and this was observed in both conditions. The extended model that includes dispersion effects and the macrovascular component has been shown to provide the best fit to both datasets. Conclusion: Our results support the use of extended models that include the macrovascular component and dispersion effects when modelling multiple-PLD pCASL data.
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spelling pubmed-102506622023-06-10 Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI Pinto, Joana Blockley, Nicholas P. Harkin, James W. Bulte, Daniel P. Front Physiol Physiology Introduction: Cerebral blood flow (CBF) is an important physiological parameter that can be quantified non-invasively using arterial spin labelling (ASL) imaging. Although most ASL studies are based on single-timepoint strategies, multi-timepoint approaches (multiple-PLD) in combination with appropriate model fitting strategies may be beneficial not only to improve CBF quantification but also to retrieve other physiological information of interest. Methods: In this work, we tested several kinetic models for the fitting of multiple-PLD pCASL data in a group of 10 healthy subjects. In particular, we extended the standard kinetic model by incorporating dispersion effects and the macrovascular contribution and assessed their individual and combined effect on CBF quantification. These assessments were performed using two pseudo-continuous ASL (pCASL) datasets acquired in the same subjects but during two conditions mimicking different CBF dynamics: normocapnia and hypercapnia (achieved through a CO(2) stimulus). Results: All kinetic models quantified and highlighted the different CBF spatiotemporal dynamics between the two conditions. Hypercapnia led to an increase in CBF whilst decreasing arterial transit time (ATT) and arterial blood volume (aBV). When comparing the different kinetic models, the incorporation of dispersion effects yielded a significant decrease in CBF (∼10–22%) and ATT (∼17–26%), whilst aBV (∼44–74%) increased, and this was observed in both conditions. The extended model that includes dispersion effects and the macrovascular component has been shown to provide the best fit to both datasets. Conclusion: Our results support the use of extended models that include the macrovascular component and dispersion effects when modelling multiple-PLD pCASL data. Frontiers Media S.A. 2023-05-26 /pmc/articles/PMC10250662/ /pubmed/37304817 http://dx.doi.org/10.3389/fphys.2023.1142359 Text en Copyright © 2023 Pinto, Blockley, Harkin and Bulte. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Pinto, Joana
Blockley, Nicholas P.
Harkin, James W.
Bulte, Daniel P.
Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title_full Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title_fullStr Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title_full_unstemmed Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title_short Modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling MRI
title_sort modelling spatiotemporal dynamics of cerebral blood flow using multiple-timepoint arterial spin labelling mri
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250662/
https://www.ncbi.nlm.nih.gov/pubmed/37304817
http://dx.doi.org/10.3389/fphys.2023.1142359
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