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PMID: 36842347 Published · ppublish English Case Reports Journal Article

On the nonlinear relationship between wall shear stress topology and multi-directionality in coronary atherosclerosis.

Computer methods and programs in biomedicine ·Vol. 231 ·2023-04-00 ·页码 107418

Carpenter HJ, Ghayesh MH, Zander AC, Psaltis PJ

Abstract

In this paper we investigate twelve multi-directional/topological wall shear stress (WSS) derived metrics and their relationships with the formation of coronary plaques in both computational fluid dynamics (CFD) and dynamic fluid-structure interaction (FSI) frameworks. While low WSS is one of the most established biomechanical markers associated with coronary atherosclerosis progression, alone it is limited. Multi-directional and topological WSS derived metrics have been shown to be important in atherosclerosis related mechanotransduction and near-wall transport processes. However, the relationships between these twelve WSS metrics and the influence of both FSI simulations and coronary dynamics is understudied. We first investigate the relationships between these twelve WSS derived metrics, stenosis percentage and lesion length through a parametric, transient CFD study. Secondly, we extend the parametric study to FSI, both with and without the addition of coronary dynamics, and assess their correlations. Finally, we present the case of a patient who underwent invasive coronary angiography and optical coherence tomography imaging at two time points 18 months apart. Associations between each of the twelve WSS derived metrics in CFD, static FSI and dynamic FSI simulations were assessed against areas of positive/negative vessel remodelling, and changes in plaque morphology. 22-32% stenosis was the threshold beyond which adverse multi-directional/topological WSS results. Each metric produced a different relationship with changing stenoses and lesion length. Transient haemodynamics was impacted by coronary dynamics, with the topological shear variation index suppressed by up to 94%. These changes appear more critical at smaller stenosis levels, suggesting coronary dynamics could play a role in the earlier stages of atherosclerosis development. In the patient case, both dynamics and FSI vs CFD changes altered associations with measured changes in plaque morphology. An appendix of the linear fits between the various FSI- and CFD-based simulations is provided to assist in scaling CFD-based results to resemble the compliant walled characteristics of FSI more accurately. These results highlight the potential for coronary dynamics to alter multi-directional/topological WSS metrics which could impact associations with changes in coronary atherosclerosis over time. These results warrant further investigation in a wider range of morphological settings and longitudinal cohort studies in the future.

Keywords
Atherosclerosis Computational fluid dynamics Coronary artery Dynamics Fluid-structure interaction Plaque progression Topology Wall shear stress
MeSH 主题词
Humans Atherosclerosis/diagnostic imaging,pathology Nonlinear Dynamics Coronary Disease/diagnostic imaging,pathology Plaque, Atherosclerotic/diagnostic imaging
作者与单位
共 4 位作者,点击展开单位 / ORCID
Carpenter Harry J
School of Mechanical Engineering, University of Adelaide, Adelaide, South Australia 5005, Australia. Electronic address: [email protected].
Ghayesh Mergen H
School of Mechanical Engineering, University of Adelaide, Adelaide, South Australia 5005, Australia. Electronic address: [email protected].
Zander Anthony C
School of Mechanical Engineering, University of Adelaide, Adelaide, South Australia 5005, Australia.
Psaltis Peter J
Vascular Research Centre, Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia 5000, Australia; Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5005, Australia; Department of Cardiology, Central Adelaide Local Health Network, Adelaide, South Australia 5000, Australia.
Article Info
Journal
Computer methods and programs in biomedicine
Abbr.
Comput Methods Programs Biomed
ISSN
1872-7565
Published
2023-04-00
电子出版
2023-00-20
页码
107418
Language
English
Country/Region
Ireland
NLM ID
8506513
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