Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.

The genesis, growth, and rupture of intracranial aneurysms (IAs) involve physics at the molecular, cellular, blood vessel, and organ levels that occur over time scales ranging from seconds to years. Comprehensive mathematical modeling of IAs, therefore, requires the description and integration of ev...

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Main Authors: Ho, H, Suresh, V, Kang, W, Cooling, M, Watton, P, Hunter, P
Format: Journal article
Language:English
Published: 2011
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author Ho, H
Suresh, V
Kang, W
Cooling, M
Watton, P
Hunter, P
author_facet Ho, H
Suresh, V
Kang, W
Cooling, M
Watton, P
Hunter, P
author_sort Ho, H
collection OXFORD
description The genesis, growth, and rupture of intracranial aneurysms (IAs) involve physics at the molecular, cellular, blood vessel, and organ levels that occur over time scales ranging from seconds to years. Comprehensive mathematical modeling of IAs, therefore, requires the description and integration of events across length and time scales that span many orders of magnitude. In this letter, we outline a strategy for mulstiscale modeling of IAs that involves the construction of individual models at each relevant scale and their subsequent combination into an integrative model that captures the overall complexity of IA development. An example of the approach is provided using three models operating at different length and time scales: 1) shear stress induced nitric oxide production; 2) smooth muscle cell apoptosis; and 3) fluid-structure-growth modeling. A computational framework for combining them is presented. We conclude with a discussion of the advantages and challenges of the approach.
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spelling oxford-uuid:39174e70-d0d8-4ff3-98e6-344dbdb10e0a2022-03-26T13:53:37ZMultiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:39174e70-d0d8-4ff3-98e6-344dbdb10e0aEnglishSymplectic Elements at Oxford2011Ho, HSuresh, VKang, WCooling, MWatton, PHunter, PThe genesis, growth, and rupture of intracranial aneurysms (IAs) involve physics at the molecular, cellular, blood vessel, and organ levels that occur over time scales ranging from seconds to years. Comprehensive mathematical modeling of IAs, therefore, requires the description and integration of events across length and time scales that span many orders of magnitude. In this letter, we outline a strategy for mulstiscale modeling of IAs that involves the construction of individual models at each relevant scale and their subsequent combination into an integrative model that captures the overall complexity of IA development. An example of the approach is provided using three models operating at different length and time scales: 1) shear stress induced nitric oxide production; 2) smooth muscle cell apoptosis; and 3) fluid-structure-growth modeling. A computational framework for combining them is presented. We conclude with a discussion of the advantages and challenges of the approach.
spellingShingle Ho, H
Suresh, V
Kang, W
Cooling, M
Watton, P
Hunter, P
Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title_full Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title_fullStr Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title_full_unstemmed Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title_short Multiscale modeling of intracranial aneurysms: cell signaling, hemodynamics, and remodeling.
title_sort multiscale modeling of intracranial aneurysms cell signaling hemodynamics and remodeling
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