Cellular Heterogeneity in the Atria: An In Silico Study in the Impact on Reentries

J. Elliott, Daniele Cinque, L. Mainardi, J. F. R. Matas
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Abstract

In-silico modelling is increasingly relied upon to gain new insights into the underlying mechanisms of atrial fibrillation. Due to the complex nature of the atria, insilico models typically exclude cellular heterogeneity. One question that remains unanswered is the impact of cellular heterogeneity on reentrant mechanisms and in the vulnerable window (VW). This study aims to present the impact of cellular heterogeneity on the AF mechanisms and susceptibility to re-entry behaviour. Cellular heterogeneity was introduced into the whole atrial model using the population of models approach and regionally specific node assignment. Each atrial model was stimulated from the SA node, followed by a series of rapid-paced ectopic beats at one of three locations in the left atria. Results showed a small, insignificant increase in reentrant frequency as a result of cellular heterogeneity, with only minor changes to the re-entrant circuit. However, the vulnerable window was significantly impacted through the introduction of cellular heterogeneity. The results suggest that cellular heterogeneity in the atrial model resulted in an increased VW for reentry depending on EB location. This suggests that local cellular heterogeneity plays a significant role in the susceptibility to re-entries, but does not significantly impact the path or frequency of re-entries.
心房细胞异质性:对再入影响的计算机研究
在计算机模拟越来越依赖于获得新的见解心房颤动的潜在机制。由于心房的复杂性,硅模型通常排除细胞异质性。一个尚未解决的问题是细胞异质性对可重入机制和脆弱窗口(VW)的影响。本研究旨在揭示细胞异质性对房颤机制和再入行为易感性的影响。利用模型群体方法和区域特异性节点分配,将细胞异质性引入整个心房模型。每个心房模型从窦房结刺激,随后在左心房的三个位置之一进行一系列快节奏异位搏动。结果显示,由于细胞的异质性,重入频率有微小的、不显著的增加,而重入电路只有微小的变化。然而,脆弱窗口通过引入细胞异质性而受到显著影响。结果表明,心房模型的细胞异质性导致EB位置不同的再入VW增加。这表明,局部细胞异质性在重新进入的易感性中起着重要作用,但对重新进入的路径或频率没有显著影响。
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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