Computational modeling of atherosclerotic plaque progression through an efficient 3D agent-based modeling approach

Panagiota I. Tsompou, Vassiliki T. Potsika, N. Petrović, V. Pezoulas, P. Siogkas, V. Tsakanikas, Dimitrios Pleouras, Michalis Papafaklis, Sotiris Nikopoulos, A. Sakellarios, D. Fotiadis
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Abstract

Since atherosclerosis has been declared as the leading cause of mortality worldwide, the imminent need for the design and development of straightforward computational modeling workflows to improve the existing cardiovascular disease risk stratification models is more important than ever. Agent-based modelling (ABM) is a promising computational approach which can be utilized for decision making in various domains from the healthcare sector to industrial applications. In the present study, we propose a straightforward approach for atheromatic plaque progression in the coronary and peripheral arteries using specialized mathematical models and computational simulations which will enable the accurate prediction of the cardiovascular disease evolution. The model incorporates the realistic 3D geometry of the artery and is the first ABM implemented in C#. According to our results, the 3D ABM was able to simulate the Trans Endothelial Migration of Lymphocytes, Monocytes and Neutrophils, the artery wall cells, endothelium cells and plaque cells reducing the time step for each cycle from 40 seconds to 0.04 seconds per cycle.
通过一种高效的基于agent的3D建模方法对动脉粥样硬化斑块进展进行计算建模
由于动脉粥样硬化已被宣布为世界范围内死亡的主要原因,设计和开发直接的计算建模工作流程以改进现有心血管疾病风险分层模型的迫切需要比以往任何时候都更加重要。基于代理的建模(ABM)是一种很有前途的计算方法,可用于从医疗保健部门到工业应用的各个领域的决策制定。在本研究中,我们提出了一种直接的方法来研究冠状动脉和外周动脉粥样硬化斑块的进展,使用专门的数学模型和计算模拟,这将能够准确预测心血管疾病的演变。该模型结合了动脉的真实3D几何形状,是第一个用c#实现的ABM。根据我们的研究结果,3D ABM能够模拟淋巴细胞、单核细胞和中性粒细胞、动脉壁细胞、内皮细胞和斑块细胞的跨内皮迁移,将每个周期的时间步长从40秒缩短到0.04秒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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