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Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus
Over 75% of abdominal aortic aneurysms harbor an intraluminal thrombus, and increasing evidence suggests that biologically active thrombus contributes to the natural history of these potentially lethal lesions. Thrombus formation depends on the local hemodynamics, which in turn depends on morphologi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125404/ https://www.ncbi.nlm.nih.gov/pubmed/30185838 http://dx.doi.org/10.1038/s41598-018-31637-6 |
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author | Bhagavan, D. Di Achille, P. Humphrey, J. D. |
author_facet | Bhagavan, D. Di Achille, P. Humphrey, J. D. |
author_sort | Bhagavan, D. |
collection | PubMed |
description | Over 75% of abdominal aortic aneurysms harbor an intraluminal thrombus, and increasing evidence suggests that biologically active thrombus contributes to the natural history of these potentially lethal lesions. Thrombus formation depends on the local hemodynamics, which in turn depends on morphological features of the aneurysm and near vasculature. We previously presented a hemodynamically motivated “thrombus formation potential” that predicts where and when thrombus might form. Herein, we combine detailed studies of the three-dimensional hemodynamics with methods of sparse grid collocation and interpolation via kriging to examine roles of five key morphological features of aneurysms on thrombus formation: lesion diameter, axial position, length, curvature, and renal artery position. Computational simulations suggest that maximum diameter is a key determinant of thrombogenicity, but other morphological features modulate this dependence. More distally located lesions tend to have a higher thrombus formation potential and shorter lesions tend to have a higher potential than longer lesions, given the same aneurysmal dilatation. Finally, movement of vortical structures through the infrarenal aorta and lesion can significantly affect thrombogenicity. Formation of intraluminal thrombus within an evolving abdominal aortic aneurysm thus depends on coupled morphological features, not all intuitive, and computational simulations can be useful for predicting thrombogenesis. |
format | Online Article Text |
id | pubmed-6125404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61254042018-09-10 Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus Bhagavan, D. Di Achille, P. Humphrey, J. D. Sci Rep Article Over 75% of abdominal aortic aneurysms harbor an intraluminal thrombus, and increasing evidence suggests that biologically active thrombus contributes to the natural history of these potentially lethal lesions. Thrombus formation depends on the local hemodynamics, which in turn depends on morphological features of the aneurysm and near vasculature. We previously presented a hemodynamically motivated “thrombus formation potential” that predicts where and when thrombus might form. Herein, we combine detailed studies of the three-dimensional hemodynamics with methods of sparse grid collocation and interpolation via kriging to examine roles of five key morphological features of aneurysms on thrombus formation: lesion diameter, axial position, length, curvature, and renal artery position. Computational simulations suggest that maximum diameter is a key determinant of thrombogenicity, but other morphological features modulate this dependence. More distally located lesions tend to have a higher thrombus formation potential and shorter lesions tend to have a higher potential than longer lesions, given the same aneurysmal dilatation. Finally, movement of vortical structures through the infrarenal aorta and lesion can significantly affect thrombogenicity. Formation of intraluminal thrombus within an evolving abdominal aortic aneurysm thus depends on coupled morphological features, not all intuitive, and computational simulations can be useful for predicting thrombogenesis. Nature Publishing Group UK 2018-09-05 /pmc/articles/PMC6125404/ /pubmed/30185838 http://dx.doi.org/10.1038/s41598-018-31637-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bhagavan, D. Di Achille, P. Humphrey, J. D. Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title | Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title_full | Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title_fullStr | Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title_full_unstemmed | Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title_short | Strongly Coupled Morphological Features of Aortic Aneurysms Drive Intraluminal Thrombus |
title_sort | strongly coupled morphological features of aortic aneurysms drive intraluminal thrombus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125404/ https://www.ncbi.nlm.nih.gov/pubmed/30185838 http://dx.doi.org/10.1038/s41598-018-31637-6 |
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