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建立心脏微循环模型以模拟冠状动脉血流和 3D 心肌灌注。

Modeling cardiac microcirculation for the simulation of coronary flow and 3D myocardial perfusion.

机构信息

LABS, Dipartimento di Chimica, Materiali e Ingegneria Chimica Giulio Natta, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan, 20133, Italy.

MOX, Dipartimento di Matematica, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan, 20133, Italy.

出版信息

Biomech Model Mechanobiol. 2024 Dec;23(6):1863-1888. doi: 10.1007/s10237-024-01873-z. Epub 2024 Jul 12.

DOI:10.1007/s10237-024-01873-z
PMID:38995488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11554812/
Abstract

Accurate modeling of blood dynamics in the coronary microcirculation is a crucial step toward the clinical application of in silico methods for the diagnosis of coronary artery disease. In this work, we present a new mathematical model of microcirculatory hemodynamics accounting for microvasculature compliance and cardiac contraction; we also present its application to a full simulation of hyperemic coronary blood flow and 3D myocardial perfusion in real clinical cases. Microvasculature hemodynamics is modeled with a compliant multi-compartment Darcy formulation, with the new compliance terms depending on the local intramyocardial pressure generated by cardiac contraction. Nonlinear analytical relationships for vessels distensibility are included based on experimental data, and all the parameters of the model are reformulated based on histologically relevant quantities, allowing a deeper model personalization. Phasic flow patterns of high arterial inflow in diastole and venous outflow in systole are obtained, with flow waveforms morphology and pressure distribution along the microcirculation reproduced in accordance with experimental and in vivo measures. Phasic diameter change for arterioles and capillaries is also obtained with relevant differences depending on the depth location. Coronary blood dynamics exhibits a disturbed flow at the systolic onset, while the obtained 3D perfusion maps reproduce the systolic impediment effect and show relevant regional and transmural heterogeneities in myocardial blood flow (MBF). The proposed model successfully reproduces microvasculature hemodynamics over the whole heartbeat and along the entire intramural vessels. Quantification of phasic flow patterns, diameter changes, regional and transmural heterogeneities in MBF represent key steps ahead in the direction of the predictive simulation of cardiac perfusion.

摘要

准确模拟冠状动脉微循环中的血液动力学是将计算机模拟方法应用于冠状动脉疾病诊断的关键步骤。在这项工作中,我们提出了一个新的微血管血液动力学数学模型,该模型考虑了微血管顺应性和心脏收缩;我们还将其应用于对真实临床病例中充血性冠状动脉血流和 3D 心肌灌注的全模拟。微血管血液动力学采用顺应性多腔隙达西公式进行建模,新的顺应性项取决于心脏收缩产生的局部心肌内压力。根据实验数据包括了血管可扩展性的非线性解析关系,并且根据组织学相关数量重新构建了模型的所有参数,允许更深层次的模型个性化。在舒张期有高动脉流入和收缩期有静脉流出的相位流动模式,流动波形形态和微循环沿线的压力分布与实验和体内测量结果一致。还获得了小动脉和毛细血管的相位直径变化,其差异与深度位置有关。冠状动脉血液动力学在收缩期开始时表现出紊乱的流动,而获得的 3D 灌注图再现了收缩期的阻碍效应,并显示了心肌血流 (MBF) 中的相关区域和跨壁异质性。所提出的模型成功地在整个心跳周期内和整个壁内血管上再现了微血管血液动力学。相位流动模式、直径变化、MBF 中的区域和跨壁异质性的定量分析代表了向心脏灌注预测模拟方向迈出的关键一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/a67b0ea123f9/10237_2024_1873_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/a67b0ea123f9/10237_2024_1873_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/e91c441b1e20/10237_2024_1873_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/4765e190a43d/10237_2024_1873_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/c9ae5511a4c8/10237_2024_1873_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/ea05d6c0f4e6/10237_2024_1873_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/87cae0ca38e9/10237_2024_1873_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/11554812/a67b0ea123f9/10237_2024_1873_Fig7_HTML.jpg

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