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A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation
BACKGROUND: The Circle of Willis (CoW) is the most important collateral pathway of the cerebral artery. The present study aims to investigate the collateral capacity of CoW with anatomical variation when unilateral internalcarotid artery (ICA) is occluded. METHODS: Basing on MRI data, we have recons...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306100/ https://www.ncbi.nlm.nih.gov/pubmed/25603312 http://dx.doi.org/10.1186/1475-925X-14-S1-S11 |
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author | Ren, Yuan Chen, Qiang Li, Zhi-Yong |
author_facet | Ren, Yuan Chen, Qiang Li, Zhi-Yong |
author_sort | Ren, Yuan |
collection | PubMed |
description | BACKGROUND: The Circle of Willis (CoW) is the most important collateral pathway of the cerebral artery. The present study aims to investigate the collateral capacity of CoW with anatomical variation when unilateral internalcarotid artery (ICA) is occluded. METHODS: Basing on MRI data, we have reconstructed eight 3D models with variations in the posterior circulation of the CoW and set four different degrees of stenosis in the right ICA, namely 24%, 43%, 64% and 79%, respectively. Finally, a total of 40 models are performed with computational fluid dynamics simulations. All of the simulations share the same boundary condition with static pressure and the volume flow rate (VFR) are obtained to evaluate their collateral capacity. RESULTS: As for the middle cerebral artery (MCA) and the anterior cerebral artery (ACA), the transitional-type model possesses the best collateral capacity. But for the posterior cerebral artery (PCA), unilateral stenosis of ICA has the weakest influence on the unilateral posterior communicating artery (PCoA) absent model. We also find that the full fetal-type posterior circle of Willis is an utmost dangerous variation which must be paid more attention. CONCLUSION: The results demonstrate that different models have different collateral capacities in coping stenosis of unilateral ICA and these differences can be reflected by different outlets. The study could be used as a reference for neurosurgeon in choosing the best treatment strategy. |
format | Online Article Text |
id | pubmed-4306100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43061002015-02-12 A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation Ren, Yuan Chen, Qiang Li, Zhi-Yong Biomed Eng Online Research BACKGROUND: The Circle of Willis (CoW) is the most important collateral pathway of the cerebral artery. The present study aims to investigate the collateral capacity of CoW with anatomical variation when unilateral internalcarotid artery (ICA) is occluded. METHODS: Basing on MRI data, we have reconstructed eight 3D models with variations in the posterior circulation of the CoW and set four different degrees of stenosis in the right ICA, namely 24%, 43%, 64% and 79%, respectively. Finally, a total of 40 models are performed with computational fluid dynamics simulations. All of the simulations share the same boundary condition with static pressure and the volume flow rate (VFR) are obtained to evaluate their collateral capacity. RESULTS: As for the middle cerebral artery (MCA) and the anterior cerebral artery (ACA), the transitional-type model possesses the best collateral capacity. But for the posterior cerebral artery (PCA), unilateral stenosis of ICA has the weakest influence on the unilateral posterior communicating artery (PCoA) absent model. We also find that the full fetal-type posterior circle of Willis is an utmost dangerous variation which must be paid more attention. CONCLUSION: The results demonstrate that different models have different collateral capacities in coping stenosis of unilateral ICA and these differences can be reflected by different outlets. The study could be used as a reference for neurosurgeon in choosing the best treatment strategy. BioMed Central 2015-01-09 /pmc/articles/PMC4306100/ /pubmed/25603312 http://dx.doi.org/10.1186/1475-925X-14-S1-S11 Text en Copyright © 2015 Ren et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ren, Yuan Chen, Qiang Li, Zhi-Yong A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title | A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title_full | A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title_fullStr | A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title_full_unstemmed | A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title_short | A 3D numerical study of the collateral capacity of the circle of Willis with anatomical variation in the posterior circulation |
title_sort | 3d numerical study of the collateral capacity of the circle of willis with anatomical variation in the posterior circulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306100/ https://www.ncbi.nlm.nih.gov/pubmed/25603312 http://dx.doi.org/10.1186/1475-925X-14-S1-S11 |
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