建立动静脉瘘血管壁振动的生理模型。

IF 3 3区 医学 Q2 BIOPHYSICS Biomechanics and Modeling in Mechanobiology Pub Date : 2024-07-08 DOI:10.1007/s10237-024-01865-z
Luca Soliveri, David Bruneau, Johannes Ring, Michela Bozzetto, Andrea Remuzzi, Kristian Valen-Sendstad
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引用次数: 0

摘要

血液透析动静脉瘘(AVF)失效背后的机理仍然鲜为人知,尽管以前曾努力将血液动力学的改变与血管重塑联系起来。我们最近证明了过渡流会诱发动静脉内瘘壁的高频振动,尽管我们使用的是简化模型。本研究解决了我们最初的流固耦合(FSI)方法的主要局限性,旨在使用更逼真的模型评估振动响应。通过无对比度磁共振成像生成了三维动静脉瘘几何图形,并进行了高保真 FSI 模拟。模拟中加入了患者特异性流入量和压力,并使用实验数据拟合了三期穆尼-里夫林模型。血管周围组织的粘弹性效应采用罗宾边界条件建模。脉冲式流入和压力导致静脉位移(+ 400 %)和应变(+ 317 %)大幅增加,最大频谱频率高于 -42 dB(从 200 Hz 到 500 Hz)。从 Saint Venant-Kirchhoff 模型过渡到 Mooney-Rivlin 模型,导致位移幅度超过 10 微米,并对应变产生了重大影响(+ 116 %)。罗宾边界条件极大地抑制了高频位移(- 60%)。加入静脉组织特性后,振动增加了 91%,频率高达 700 赫兹,最大应变为 0.158。值得注意的是,我们的研究结果表明,静脉内弯处的局部振动水平较高,而这一部位众所周知正经历着明显的重塑。我们的研究结果与实验和临床报告中的淤血和颤动一致,强调了采用生理学上可信的建模方法来研究静脉壁振动在动静脉瓣膜重塑和失效中的作用的重要性。
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Toward a physiological model of vascular wall vibrations in the arteriovenous fistula

The mechanism behind hemodialysis arteriovenous fistula (AVF) failure remains poorly understood, despite previous efforts to correlate altered hemodynamics with vascular remodeling. We have recently demonstrated that transitional flow induces high-frequency vibrations in the AVF wall, albeit with a simplified model. This study addresses the key limitations of our original fluid–structure interaction (FSI) approach, aiming to evaluate the vibration response using a more realistic model. A 3D AVF geometry was generated from contrast-free MRI and high-fidelity FSI simulations were performed. Patient-specific inflow and pressure were incorporated, and a three-term Mooney–Rivlin model was fitted using experimental data. The viscoelastic effect of perivascular tissue was modeled with Robin boundary conditions. Prescribing pulsatile inflow and pressure resulted in a substantial increase in vein displacement (\(+400\)%) and strain (\(+317\)%), with a higher maximum spectral frequency becoming visible above -42 dB (from 200 to 500 Hz). Transitioning from Saint Venant–Kirchhoff to Mooney–Rivlin model led to displacement amplitudes exceeding 10 micrometers and had a substantial impact on strain (\(+116\)%). Robin boundary conditions significantly damped high-frequency displacement (\(-60\)%). Incorporating venous tissue properties increased vibrations by 91%, extending up to 700 Hz, with a maximum strain of 0.158. Notably, our results show localized, high levels of vibration at the inner curvature of the vein, a site known for experiencing pronounced remodeling. Our findings, consistent with experimental and clinical reports of bruits and thrills, underscore the significance of incorporating physiologically plausible modeling approaches to investigate the role of wall vibrations in AVF remodeling and failure.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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