Mechano-chemo-biological model of atherosclerosis formation based on the outside-in theory

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dc.identifier.uri http://dx.doi.org/10.15488/17012
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/17140
dc.contributor.author Gierig, Meike
dc.contributor.author Tragoudas, Alexandros
dc.contributor.author Haverich, Axel
dc.contributor.author Wriggers, Peter
dc.date.accessioned 2024-04-10T08:51:04Z
dc.date.available 2024-04-10T08:51:04Z
dc.date.issued 2023
dc.identifier.citation Gierig, M.; Tragoudas, A.; Haverich, A.; Wriggers, P.: Mechano-chemo-biological model of atherosclerosis formation based on the outside-in theory. In: Biomechanics and Modeling in Mechanobiology 23 (2024), Nr. 2, S. 539-552. DOI: https://doi.org/10.1007/s10237-023-01790-7
dc.description.abstract Atherosclerosis is a disease in blood vessels that often results in plaque formation and lumen narrowing. It is an inflammatory response of the tissue caused by disruptions in the vessel wall nourishment. Blood vessels are nourished by nutrients originating from the blood of the lumen. In medium-sized and larger vessels, nutrients are additionally provided from outside through a network of capillaries called vasa vasorum. It has recently been hypothesized (Haverich in Circulation 135:205–207, 2017) that the root of atherosclerotic diseases is the malfunction of the vasa vasorum. This, so-called outside-in theory, is supported by a recently developed numerical model (Soleimani et al. in Arch Comput Methods Eng 28:4263–4282, 2021) accounting for the inflammation initiation in the adventitial layer of the blood vessel. Building on the previous findings, this work proposes an extended material model for atherosclerosis formation that is based on the outside-in theory. Beside the description of growth kinematics and nutrient diffusion, the roles of monocytes, macrophages, foam cells, smooth muscle cells and collagen are accounted for in a nonlinear continuum mechanics framework. Cells are activated due to a lack of vessel wall nourishment and proliferate, migrate, differentiate and synthesize collagen, leading to the formation of a plaque. Numerical studies show that the onset of atherosclerosis can qualitatively be reproduced and back the new theory. eng
dc.language.iso eng
dc.publisher Berlin ; Heidelberg ; New York, NY : Springer
dc.relation.ispartofseries Biomechanics and Modeling in Mechanobiology 23 (2024), Nr. 2
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0
dc.subject Atherosclerosis eng
dc.subject Finite element method eng
dc.subject Mechanobiology eng
dc.subject Outside-in theory eng
dc.subject.ddc 570 | Biowissenschaften, Biologie
dc.subject.ddc 540 | Chemie
dc.title Mechano-chemo-biological model of atherosclerosis formation based on the outside-in theory eng
dc.type Article
dc.type Text
dc.relation.essn 1617-7940
dc.relation.issn 1617-7959
dc.relation.doi https://doi.org/10.1007/s10237-023-01790-7
dc.bibliographicCitation.issue 2
dc.bibliographicCitation.volume 23
dc.bibliographicCitation.date 2024
dc.bibliographicCitation.firstPage 539
dc.bibliographicCitation.lastPage 552
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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