Department of Physiology II, Kanazawa Medical University, Uchinada 920-0293, Japan.
Department of Bioinformatics, College of Life Sciences, Ritsumeikan University, Kusatsu 525-8577, Japan.
Comput Methods Programs Biomed. 2023 Oct;240:107722. doi: 10.1016/j.cmpb.2023.107722. Epub 2023 Jul 15.
Excessive prolongation of QT interval on ECGs in patients with congenital/acquired long QT syndrome and heart failure is a sign suggesting the development of early afterdepolarization (EAD), an abnormal repolarization in the action potential of ventricular cardiomyocytes. The development of EAD has been believed to be a trigger for fatal tachyarrhythmia, which can be a risk for sudden cardiac death. The role of EAD in triggering ventricular tachycardia (VT) remains unclear. The aim of this study was to elucidate the mechanism of EAD-induced triggered activity formation that leads to the VT such as Torsades de Pointes.
We investigated the relationship between EAD and tachyarrhythmia initiation by constructing homogeneous myocardial sheet models consisting of the mid-myocardial cell version of a human ventricular myocyte model and performing simulations of excitation propagation.
A solitary island-like (clustering) occurrence of EADs in the homogeneous myocardial sheet could induce a focal excitation wave. However, reentrant excitation, an entity of tachyarrhythmia, was not able to be triggered regardless of the EAD cluster size when the focal excitation wave formed a repolarization potential difference boundary consisting of only a convex surface. The discontinuous distribution of multiple EAD clusters in the ventricular tissue formed a specific repolarization heterogeneity due to the repolarization potential difference, the shape of which depended on EAD cluster size and placed intervals. We found that the triggered activity was formed in such a manner that the repolarization potential difference boundary included a concave surface.
The formation of triggered activity that led to tachyarrhythmia required not only the occurrence of EAD onset-mediated focal excitation wave but also a repolarization heterogeneity-based specific repolarization potential difference boundary shape formed within the tissue.
心电图上先天性/获得性长 QT 综合征和心力衰竭患者 QT 间期延长过度是早期后除极(EAD)发生的标志,这是心室肌细胞动作电位中异常复极化的一种表现。EAD 的发生被认为是致命性心动过速的触发因素,可能导致心源性猝死。EAD 在触发室性心动过速(VT)中的作用尚不清楚。本研究旨在阐明导致尖端扭转型室性心动过速(Torsades de Pointes)等 VT 的 EAD 诱发触发活动形成的机制。
我们通过构建由人心室肌细胞模型的中层心肌细胞版本组成的均匀心肌片模型,并进行兴奋传播模拟,研究 EAD 与心动过速起始之间的关系。
在均匀心肌片上,EAD 呈孤立岛状(簇状)发生时,可以诱发局灶兴奋波。然而,当局灶兴奋波形成仅由凸面组成的复极电位差边界时,无论 EAD 簇的大小如何,都不能引发折返兴奋,即心动过速的实体。心室组织中多个 EAD 簇的不连续分布由于复极电位差形成了特定的复极异质性,其形状取决于 EAD 簇的大小和放置间隔。我们发现,触发活动的形成方式是复极电位差边界包含凹面。
导致心动过速的触发活动的形成不仅需要 EAD 起始介导的局灶兴奋波的发生,还需要组织内形成基于复极异质性的特定复极电位差边界形状。