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A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI

Mapping the complex heterogeneity of vascular tissue in the brain is important for understanding cerebrovascular disease. In this translational study, we build on previous work using vessel architectural imaging (VAI) and present a theoretical framework for determining cerebral vascular function and...

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Autores principales: Digernes, Ingrid, Bjørnerud, Atle, Vatnehol, Svein Are S, Løvland, Grete, Courivaud, Frédéric, Vik-Mo, Einar, Meling, Torstein R, Emblem, Kyrre E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444554/
https://www.ncbi.nlm.nih.gov/pubmed/28273722
http://dx.doi.org/10.1177/0271678X17694187
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author Digernes, Ingrid
Bjørnerud, Atle
Vatnehol, Svein Are S
Løvland, Grete
Courivaud, Frédéric
Vik-Mo, Einar
Meling, Torstein R
Emblem, Kyrre E
author_facet Digernes, Ingrid
Bjørnerud, Atle
Vatnehol, Svein Are S
Løvland, Grete
Courivaud, Frédéric
Vik-Mo, Einar
Meling, Torstein R
Emblem, Kyrre E
author_sort Digernes, Ingrid
collection PubMed
description Mapping the complex heterogeneity of vascular tissue in the brain is important for understanding cerebrovascular disease. In this translational study, we build on previous work using vessel architectural imaging (VAI) and present a theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast magnetic resonance imaging (MRI). Our tissue model covers realistic structural architectures for vessel branching and orientations, as well as a range of hemodynamic scenarios for blood flow, capillary transit times and oxygenation. In a typical image voxel, our findings show that the apparent MRI relaxation rates are independent of the mean vessel orientation and that the vortex area, a VAI-based parameter, is determined by the relative oxygen saturation level and the vessel branching of the tissue. Finally, in both simulated and patient data, we show that the relative distributions of the vortex area parameter as a function of capillary transit times show unique characteristics in normal-appearing white and gray matter tissue, whereas tumour-voxels in comparison display a heterogeneous distribution. Collectively, our study presents a comprehensive framework that may serve as a roadmap for in vivo and per-voxel determination of vascular status and heterogeneity in cerebral tissue.
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spelling pubmed-54445542017-06-02 A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI Digernes, Ingrid Bjørnerud, Atle Vatnehol, Svein Are S Løvland, Grete Courivaud, Frédéric Vik-Mo, Einar Meling, Torstein R Emblem, Kyrre E J Cereb Blood Flow Metab Original Articles Mapping the complex heterogeneity of vascular tissue in the brain is important for understanding cerebrovascular disease. In this translational study, we build on previous work using vessel architectural imaging (VAI) and present a theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast magnetic resonance imaging (MRI). Our tissue model covers realistic structural architectures for vessel branching and orientations, as well as a range of hemodynamic scenarios for blood flow, capillary transit times and oxygenation. In a typical image voxel, our findings show that the apparent MRI relaxation rates are independent of the mean vessel orientation and that the vortex area, a VAI-based parameter, is determined by the relative oxygen saturation level and the vessel branching of the tissue. Finally, in both simulated and patient data, we show that the relative distributions of the vortex area parameter as a function of capillary transit times show unique characteristics in normal-appearing white and gray matter tissue, whereas tumour-voxels in comparison display a heterogeneous distribution. Collectively, our study presents a comprehensive framework that may serve as a roadmap for in vivo and per-voxel determination of vascular status and heterogeneity in cerebral tissue. SAGE Publications 2017-01-01 2017-06 /pmc/articles/PMC5444554/ /pubmed/28273722 http://dx.doi.org/10.1177/0271678X17694187 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Digernes, Ingrid
Bjørnerud, Atle
Vatnehol, Svein Are S
Løvland, Grete
Courivaud, Frédéric
Vik-Mo, Einar
Meling, Torstein R
Emblem, Kyrre E
A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title_full A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title_fullStr A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title_full_unstemmed A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title_short A theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast MRI
title_sort theoretical framework for determining cerebral vascular function and heterogeneity from dynamic susceptibility contrast mri
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444554/
https://www.ncbi.nlm.nih.gov/pubmed/28273722
http://dx.doi.org/10.1177/0271678X17694187
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