Computation in the rabbit aorta of a new metric - the transverse wall shear stress - to quantify the multidirectional character of disturbed blood flow

被引:143
作者
Peiffer, Veronique [1 ,2 ]
Sherwin, Spencer J. [1 ]
Weinberg, Peter D. [2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Aeronaut, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
Atherosclerosis; Haemodynamics; Wall shear stress; Multidirectionality; Disturbed flow; Rabbit aorta; PULSATILE FLOW; HEMODYNAMICS; PATTERNS; ARTERY; LOCALIZATION; PLAQUE;
D O I
10.1016/j.jbiomech.2013.08.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Spatial variation of the haemodynamic stresses acting on the arterial wall is commonly assumed to explain the focal development of atherosclerosis. Disturbed flow in particular is thought to play a key role. However, widely-used metrics developed to quantify its extent are unable to distinguish between uniaxial and multidirectional flows. We analysed pulsatile flow fields obtained in idealised and anatomically-realistic arterial geometries using computational fluid dynamics techniques, and in particular investigated the multidirectionality of the flow fields, capturing this aspect of near-wall blood flow with a new metric - the transverse wall shear stress (transWSS) - calculated as the time-average of wall shear stress components perpendicular to the mean flow direction. In the idealised branching geometry, multidirectional flow was observed downstream of the branch ostium, a region of flow stagnation, and to the sides of the ostium. The distribution of the transWSS was different from the pattern of traditional haemodynamic metrics and more dependent on the velocity waveform imposed at the branch outlet. In rabbit aortas, transWSS patterns were again different from patterns of traditional metrics. The near-branch pattern varied between intercostal ostia, as is the case for lesion distribution; for some branches there were striking resemblances to the age-dependent patterns of disease seen in rabbit and human aortas. The new metric may lead to improved understanding of atherogenesis. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2651 / 2658
页数:8
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