Clinic of Cardiovascular Diseases, University of Genoa, 6 Viale Benedetto XV, 16132 Genoa, Italy.
IRCCS Ospedale Policlinico San Martino Genoa-Italian Cardiovascular Network, 10 Largo Benzi, 16132 Genoa, Italy.
Biomed Res Int. 2019 Oct 30;2019:6571045. doi: 10.1155/2019/6571045. eCollection 2019.
Takotsubo syndrome (TTS) is a recently identified cardiac disease, which is far from being completely known. The aims of this narrative review are to provide a better understanding of the pathophysiological features of TTS and to update clinical findings in order to improve the management of subjects affected by this syndrome (according to the most recent consensus papers issued by the international scientific societies). We based our search on the material obtained via PubMed up to April 2019. The terms used were "Takotsubo Syndrome and Takotsubo cardiomyopathy" in combination with "heart failure, pathophysiology, complications, diagnosis, and treatment." TTS is a reversible form of ventricular dysfunction usually characterized by akinesia of the apex in the absence of obstructive coronary artery disease. In its initial phase, TTS may be indistinguishable from AMI and is usually triggered by a sudden emotional/physical stressor which abruptly increases catecholamine levels. However, the mechanisms by which catecholamines or other unidentified molecules can cause myocardial dysfunction is unknown. In-hospital stay may be hampered by various life-threatening complications, while data on long-term survival remain scarce and unclear. Furthermore, TTS may sometimes recur. We believe that TTS is clearly a much more complex condition than previously thought. Much remains to be discovered about its pathophysiologic mechanisms, the role of the link between the heart and brain and that of triggering factors and gender, and the reasons why this syndrome displays different phenotypes and sometimes recurs. Undoubtedly, preliminary evidence from pathophysiological studies (mainly genetic studies) has shown promising advances. However, prospective randomized clinical trials are still needed in order to identify and to tailor the best medical treatments for TTS patients.
应激性心肌病(Takotsubo 综合征)是一种最近才被识别的心脏疾病,人们对它的了解还远远不够。本综述的目的是提供对 Takotsubo 综合征病理生理学特征的更深入理解,并更新临床发现,以改善受这种综合征影响的患者的管理(根据国际科学协会发布的最新共识文件)。我们的检索基于截至 2019 年 4 月从 PubMed 获得的资料。使用的术语是“Takotsubo 综合征和 Takotsubo 心肌病”,并与“心力衰竭、病理生理学、并发症、诊断和治疗”结合使用。Takotsubo 综合征是一种心室功能障碍的可逆形式,通常表现为心室中部无阻塞性冠状动脉疾病时的心室中部运动不能。在其初始阶段,Takotsubo 综合征可能与 AMI 无法区分,通常由突然的情绪/身体应激源引起,这些应激源突然增加儿茶酚胺水平。然而,儿茶酚胺或其他未识别的分子如何导致心肌功能障碍的机制尚不清楚。住院期间可能会因各种危及生命的并发症而受阻,而关于长期生存的数据仍然很少且不清楚。此外,Takotsubo 综合征有时可能会复发。我们认为,Takotsubo 综合征显然比以前认为的要复杂得多。关于其病理生理机制、心脏与大脑之间的联系以及触发因素和性别所起的作用,以及为什么这种综合征表现出不同的表型,有时会复发,还有很多需要了解。毫无疑问,来自病理生理学研究(主要是遗传研究)的初步证据显示出了有希望的进展。然而,仍需要进行前瞻性随机临床试验,以确定并针对 Takotsubo 综合征患者制定最佳的治疗方法。