Study on the association of wall shear stress and vessel structural stress with atherosclerosis: An experimental animal study.


Journal

Atherosclerosis
ISSN: 1879-1484
Titre abrégé: Atherosclerosis
Pays: Ireland
ID NLM: 0242543

Informations de publication

Date de publication:
03 2021
Historique:
received: 14 05 2020
revised: 07 01 2021
accepted: 13 01 2021
pubmed: 2 2 2021
medline: 24 6 2021
entrez: 1 2 2021
Statut: ppublish

Résumé

Artery is subject to wall shear stress (WSS) and vessel structural stress (VSS) simultaneously. This study is designed to explore the role of VSS in development of atherosclerosis. Silastic collars were deployed on the carotid to create two constrictions on 13 rabbits for a distinct mechanical environment at the constriction. MRI was performed to visualize arteries' configuration. Animals with high fat (n = 9; Model-group) and normal diet (n = 4; Control-group) were sacrificed after 16 weeks. 3D fluid-structure interaction analysis was performed to quantify WSS and VSS simultaneously. Twenty plaques were found in Model-group and 3 in Control-group. In Model-group, 8 plaques located proximally to the first constriction (Region-1, close to the heart) and 7 distally to the second (Region-2, close to the head) and 5 plaques were found on the contralateral side of 3 rabbits. Plaques at Region-1 tended to be bigger than those at Region-2 and the macrophage density at these locations was comparable. Minimum time-averaged WSS (TAWSS) in Region-1 was significantly higher than that in Region-2, and both maximum oscillatory shear index (OSI) and particle relative residence time (RRT) were significantly lower. Peak and mean VSS in Region-1 were significantly higher than those in Region-2. Correlation analyses indicated that low TAWSS, high OSI and RRT were only associated with plaque in Region-2, while lesions in Region-1 were only associated with high VSS. Moreover, only VSS was associated with wall thickness of plaque-free regions in both regions. VSS might contribute to the initialization and development of atherosclerosis solely or in combination with WSS.

Sections du résumé

BACKGROUND AND AIMS
Artery is subject to wall shear stress (WSS) and vessel structural stress (VSS) simultaneously. This study is designed to explore the role of VSS in development of atherosclerosis.
METHODS
Silastic collars were deployed on the carotid to create two constrictions on 13 rabbits for a distinct mechanical environment at the constriction. MRI was performed to visualize arteries' configuration. Animals with high fat (n = 9; Model-group) and normal diet (n = 4; Control-group) were sacrificed after 16 weeks. 3D fluid-structure interaction analysis was performed to quantify WSS and VSS simultaneously.
RESULTS
Twenty plaques were found in Model-group and 3 in Control-group. In Model-group, 8 plaques located proximally to the first constriction (Region-1, close to the heart) and 7 distally to the second (Region-2, close to the head) and 5 plaques were found on the contralateral side of 3 rabbits. Plaques at Region-1 tended to be bigger than those at Region-2 and the macrophage density at these locations was comparable. Minimum time-averaged WSS (TAWSS) in Region-1 was significantly higher than that in Region-2, and both maximum oscillatory shear index (OSI) and particle relative residence time (RRT) were significantly lower. Peak and mean VSS in Region-1 were significantly higher than those in Region-2. Correlation analyses indicated that low TAWSS, high OSI and RRT were only associated with plaque in Region-2, while lesions in Region-1 were only associated with high VSS. Moreover, only VSS was associated with wall thickness of plaque-free regions in both regions.
CONCLUSIONS
VSS might contribute to the initialization and development of atherosclerosis solely or in combination with WSS.

Identifiants

pubmed: 33524908
pii: S0021-9150(21)00030-7
doi: 10.1016/j.atherosclerosis.2021.01.017
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

38-46

Subventions

Organisme : British Heart Foundation
ID : PG/11/74/29100
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/14/33562
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/19/66/34658
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/2000003/12800
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/15/26/31441
Pays : United Kingdom

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Zhongzhao Teng (Z)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom; Department of Engineering, University of Cambridge, Cambridge, United Kingdom. Electronic address: zt215@cam.ac.uk.

Shuo Wang (S)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Aziz Tokgoz (A)

Department of Engineering, University of Cambridge, Cambridge, United Kingdom.

Valentina Taviani (V)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Joseph Bird (J)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Umar Sadat (U)

Cambridge Vascular Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Yuan Huang (Y)

EPSRC Centre for Mathematical and Statistical Analysis of Multimodal Clinical Imaging, University of Cambridge, Cambridge, United Kingdom.

Andrew J Patterson (AJ)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Nichola Figg (N)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Martin J Graves (MJ)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Jonathan H Gillard (JH)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

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Classifications MeSH