{"title":"Semi-automated pipeline for generating personalised cerebrovascular models.","authors":"Alireza Sharifzadeh-Kermani, Jiantao Shen, Finbar Argus, Sergio Dempsey, Jethro Wright, Eryn Kwon, Samantha Holdsworth, Gonzalo Maso Talou, Soroush Safaei","doi":"10.1007/s10237-024-01908-5","DOIUrl":null,"url":null,"abstract":"<p><p>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 <math><mrow><mn>0.25</mn> <mo>±</mo> <mn>0.66</mn> <mo>%</mo></mrow> </math> for flow and <math><mrow><mn>13.87</mn> <mo>±</mo> <mn>18.24</mn> <mo>%</mo></mrow> </math> 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.</p>","PeriodicalId":489,"journal":{"name":"Biomechanics and Modeling in Mechanobiology","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomechanics and Modeling in Mechanobiology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s10237-024-01908-5","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
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 for flow and 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.
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.