Department of Cardiovascular Medicine, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Int J Mol Sci. 2024 Sep 23;25(18):10193. doi: 10.3390/ijms251810193.
As atrial fibrillation (AF) progresses from initial paroxysmal episodes to the persistent phase, maintaining sinus rhythm for an extended period through pharmacotherapy and catheter ablation becomes difficult. A major cause of the deteriorated treatment outcome is the atrial structural and electrophysiological heterogeneity, which AF itself can exacerbate. This heterogeneity exists or manifests in various dimensions, including anatomically segmental structural features, the distribution of histological fibrosis and the autonomic nervous system, sarcolemmal ion channels, and electrophysiological properties. All these types of heterogeneity are closely related to the development of AF. Recognizing the heterogeneity provides a valuable approach to comprehending the underlying mechanisms in the complex excitatory patterns of AF and the determining factors that govern the seemingly chaotic propagation. Furthermore, substrate modification based on heterogeneity is a potential therapeutic strategy. This review aims to consolidate the current knowledge on structural and electrophysiological atrial heterogeneity and its relation to the pathogenesis of AF, drawing insights from clinical studies, animal and cell experiments, molecular basis, and computer-based approaches, to advance our understanding of the pathophysiology and management of AF.
随着心房颤动(房颤)从初始阵发性发作进展为持续性阶段,通过药物治疗和导管消融来长时间维持窦性心律变得越来越困难。治疗效果恶化的一个主要原因是心房结构和电生理异质性,而房颤本身可以加剧这种异质性。这种异质性存在或表现在多个维度上,包括解剖分段结构特征、组织纤维化和自主神经系统的分布、肌膜离子通道和电生理特性。所有这些类型的异质性都与房颤的发展密切相关。认识到这种异质性为理解房颤复杂兴奋模式的潜在机制以及决定看似混乱传播的因素提供了有价值的方法。此外,基于异质性的基质修饰是一种有潜力的治疗策略。本综述旨在整合目前关于心房结构和电生理异质性及其与房颤发病机制关系的知识,从临床研究、动物和细胞实验、分子基础以及基于计算机的方法中汲取灵感,以增进我们对房颤病理生理学和管理的理解。