Semi-automated pipeline for generating personalised cerebrovascular models.

IF 3 3区 医学 Q2 BIOPHYSICS Biomechanics and Modeling in Mechanobiology Pub Date : 2024-11-27 DOI:10.1007/s10237-024-01908-5
Alireza Sharifzadeh-Kermani, Jiantao Shen, Finbar Argus, Sergio Dempsey, Jethro Wright, Eryn Kwon, Samantha Holdsworth, Gonzalo Maso Talou, Soroush Safaei
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Abstract

Subject-specific cerebrovascular models predict individual unmeasurable vessel haemodynamics using principles of physics, assumed constitutive laws, and measurement-deduced boundary conditions. However, the process of generating these models can be time-consuming, which is a barrier for use in time-sensitive clinical applications. In this work, we developed a semi-automated pipeline to generate anatomically and functionally personalised 0D cerebrovascular models from vasculature geometry and blood flow data. The pipeline extracts the vessel connectivity and geometric parameters from vessel segmentation to automatically generate a bond graph-based (linear and time-dependent) model of subject vasculature. Then, using a neurofuzzy control scheme, the peripheral resistances of the model are calibrated to minimise the discrepancy between measured and predicted blood flow distributions. We validated the pipeline by generating subject-specific models of the Circle of Willis (CoW) for 10 cases and compared haemodynamic predictions against acquired 4D flow MRI data. The results showed a relative error of 0.25 ± 0.66 % for flow and 13.87 ± 18.24 % for pulsatility, with a higher error for smaller vessels. We then demonstrated a use case of the model by simulating the blood flow redistribution during vascular occlusion for different CoW geometries. The results highlighted the benefit of a completely connected CoW to redistribute flow. The modular nature and rapid model generation time of this pipeline make it a promising tool for research and clinical use, where the type and structure of data are variable, and computing resources may be limited.

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生成个性化脑血管模型的半自动化管道。
特定受试者的脑血管模型利用物理学原理、假定的构成规律和测量得出的边界条件,预测单个不可测量的血管血液动力学。然而,生成这些模型的过程可能非常耗时,这阻碍了这些模型在对时间敏感的临床应用中的使用。在这项工作中,我们开发了一种半自动化管道,从血管几何和血流数据生成解剖学和功能上个性化的 0D 脑血管模型。该管道从血管分割中提取血管连通性和几何参数,自动生成基于结合图(线性和随时间变化)的受试者血管模型。然后,利用神经模糊控制方案对模型的外围阻力进行校准,以尽量减小测量血流分布与预测血流分布之间的差异。我们通过生成 10 个病例的威利斯环(CoW)特定受试者模型来验证该管道,并将血流动力学预测与获取的 4D 血流 MRI 数据进行比较。结果显示,血流的相对误差为 0.25 ± 0.66 %,脉动的相对误差为 13.87 ± 18.24 %,较小血管的误差更大。然后,我们通过模拟不同 CoW 几何结构的血管闭塞过程中的血流再分布,演示了该模型的使用案例。结果凸显了完全连通的 CoW 对血流再分布的益处。该流水线的模块化特性和快速模型生成时间使其成为研究和临床使用的理想工具,因为数据的类型和结构是可变的,而计算资源可能是有限的。
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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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