Maan Abhishek, Mansour Moussa, McManus David D, Patel Vickas V, Cheng Alan, Ruskin Jeremy N, Heist E Kevin
Division of Electrophysiology, Cardiac Arrhythmia Service, Massachusetts General Hospital, Boston, MA, 02114, USA.
Am J Cardiovasc Drugs. 2014 Dec;14(6):403-21. doi: 10.1007/s40256-014-0085-0.
Atrial fibrillation (AF) is the most common cardiac arrhythmia, contributing to increased morbidity and reduced survival through its associations with stroke and heart failure. AF contributes to a four- to fivefold increase in the risk of stroke in the general population and is responsible for 10-15 % of all ischemic strokes. Diagnosis and treatment of AF require considerable health care resources. Current therapies to restore sinus rhythm in AF are suboptimal and are limited either by their pro-arrhythmic effects or by their procedure-related complications. These limitations have necessitated identification of newer therapeutic targets to expand the treatment options. There has been a considerable amount of research interest in investigating the mechanisms of initiation and propagation of AF. Despite extensive research focused on the pathogenesis of AF, a thorough understanding of various pathways mediating initiation and propagation of AF still remains limited. Research efforts focused on the identification of these pathways and molecular mediators have generated a great degree of interest for developing more targeted therapies. This review discusses the potential therapeutic targets and the results from experimental and clinical research investigating these targets.
心房颤动(AF)是最常见的心律失常,通过与中风和心力衰竭的关联导致发病率增加和生存率降低。AF使普通人群中风风险增加四至五倍,占所有缺血性中风的10 - 15%。AF的诊断和治疗需要大量医疗资源。目前恢复AF窦性心律的疗法并不理想,要么受其促心律失常作用限制,要么受其与手术相关的并发症限制。这些局限性使得必须确定新的治疗靶点以扩大治疗选择。在研究AF的起始和传播机制方面已经有大量的研究兴趣。尽管对AF的发病机制进行了广泛研究,但对介导AF起始和传播的各种途径的透彻理解仍然有限。专注于识别这些途径和分子介质的研究工作激发了人们对开发更具针对性疗法的极大兴趣。本综述讨论了潜在的治疗靶点以及研究这些靶点的实验和临床研究结果。