Research Center, Montréal Heart Institute, Montréal, Québec, Canada; Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada.
Research Center, Montréal Heart Institute, Montréal, Québec, Canada; Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada; Institute of Pharmacology, West German Heart and Vascular Center, Faculty of Medicine, University Duisburg-Essen, Essen, Germany; Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec, Canada.
Can J Cardiol. 2018 Nov;34(11):1449-1460. doi: 10.1016/j.cjca.2018.07.475. Epub 2018 Aug 1.
Arrhythmia-induced cardiomyopathy (AIC) is characterized by left ventricular systolic dysfunction for which the primary cause is arrhythmia. The hallmark of AIC is its reversibility once the arrhythmia is properly controlled. Any tachyarrhythmia can potentially cause AIC (often called "tachycardiomyopathy"), with atrial fibrillation (AF) being by far the most common in clinical practice. The pathophysiological mechanisms underlying AIC need further clarification, but the available evidence, principally from animal models, implicates metabolic dysfunction due to increased oxygen requirements, neurohormonal adaptive mechanisms, and cellular Ca mishandling as important contributors. Tachycardia is a common denominator of most cases of AIC, but other components specific to the patient and the arrhythmia have been implicated. The diagnosis of AIC requires the exclusion of a primary causative role of other conditions such as hypertension, primary cardiomyopathies, and valve disease, which may require specific pharmacological and invasive therapies. Catheter ablation is emerging as a safe and effective alternative to antiarrhythmic medication and has an established role in the management of AIC. Recent studies showing improved cardiac function and mortality rates in patients with heart failure and concomitant AF dramatically illustrate the often-unrecognized scope of AIC and the potential benefits of interventional therapy. Major AF trials do not otherwise focus specifically on AIC, and careful analysis of the literature is necessary to appreciate the clinical characteristics and therapeutic implications. This contemporary review summarizes the current understanding of pathophysiological mechanisms underlying AIC, discusses the clinical implications, and offers a general approach to management, with a particular focus on AF-induced cardiomyopathy.
心律失常性心肌病(AIC)的特征为左心室收缩功能障碍,其主要病因是心律失常。AIC 的标志是一旦心律失常得到适当控制,即可逆转。任何快速性心律失常都可能导致 AIC(通常称为“心动过速性心肌病”),而在临床实践中,房颤(AF)是最常见的。AIC 的病理生理机制尚需进一步阐明,但现有证据主要来自动物模型,表明由于氧需求增加、神经激素适应性机制和细胞钙处理异常导致代谢功能障碍是重要的促成因素。心动过速是大多数 AIC 病例的共同特征,但其他与患者和心律失常相关的特定成分也被牵涉其中。AIC 的诊断需要排除其他疾病(如高血压、原发性心肌病和瓣膜病)的原发性致病作用,这些疾病可能需要特定的药物和介入治疗。导管消融作为抗心律失常药物的安全有效替代方法正在出现,并在 AIC 的治疗中发挥着既定作用。最近的研究表明,在心力衰竭和同时伴有 AF 的患者中,心脏功能和死亡率得到改善,这极大地说明了 AIC 的范围常常未被认识到,以及介入治疗的潜在益处。大型 AF 试验并未特别关注 AIC,因此有必要仔细分析文献,以了解其临床特征和治疗意义。本综述总结了目前对 AIC 病理生理机制的认识,讨论了其临床意义,并提供了一般的管理方法,特别关注 AF 引起的心肌病。