Shen Hua, Dong Shi-Yong, Ren Ming-Shi, Wang Rong
Division of Adult Cardiac Surgery, Department of Cardiovascular Medicine, The Sixth Medical Center, Chinese PLA General Hospital, Beijing, China.
Department of Cardiovascular Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Front Cardiovasc Med. 2022 Aug 18;9:949294. doi: 10.3389/fcvm.2022.949294. eCollection 2022.
Patients with hypertrophic cardiomyopathy (HCM) mostly experience minimal symptoms throughout their lifetime, and some individuals have an increased risk of ventricular arrhythmias and sudden cardiac death (SCD). How to identify patients with a higher risk of ventricular arrythmias and SCD is the priority in HCM research. The American College of Cardiology/American Heart Association (ACC/AHA) and the European Society of Cardiology (ESC) both recommend the use of risk algorithms to identify patients at high risk of ventricular arrhythmias, to be selected for implantation of implantable cardioverters/defibrillators (ICDs) for primary prevention of SCD, although major discrepancies exist. The present SCD risk scoring systems cannot accurately identify early-stage HCM patients with modest structural remodeling and mild disease manifestations. Unfortunately, SCD events could occur in young asymptomatic HCM patients and even as initial symptoms, prompting the determination of new risk factors for SCD. This review summarizes the studies based on patients' surgical specimens, transgenic animals, and patient-derived induced pluripotent stem cells (hiPSCs) to explore the possible molecular mechanism of ventricular arrhythmia and SCD. Ion channel remodeling, Ca2+ homeostasis abnormalities, and increased myofilament Ca2+ sensitivity may contribute to changes in action potential duration (APD), reentry circuit formation, and trigger activities, such as early aferdepolarization (EAD) or delayed afterdepolarization (DAD), leading to ventricular arrhythmia in HCM. Besides the ICD implantation, novel drugs represented by the late sodium current channel inhibitor and myosin inhibitor also shed light on the prevention of HCM-related arrhythmias. The ideal prevention strategy of SCD in early-stage HCM patients needs to be combined with gene screening, hiPSC-CM testing, machine learning, and advanced ECG studies, thus achieving individualized SCD prevention.
肥厚型心肌病(HCM)患者一生中大多症状轻微,部分个体发生室性心律失常和心源性猝死(SCD)的风险增加。如何识别室性心律失常和SCD风险较高的患者是HCM研究的重中之重。美国心脏病学会/美国心脏协会(ACC/AHA)和欧洲心脏病学会(ESC)均推荐使用风险算法来识别室性心律失常高危患者,以便选择植入植入式心脏复律除颤器(ICD)进行SCD的一级预防,尽管存在重大差异。目前的SCD风险评分系统无法准确识别结构重塑程度适中、疾病表现轻微的早期HCM患者。不幸的是,SCD事件可能发生在年轻无症状的HCM患者中,甚至作为首发症状出现,这促使人们去确定SCD的新危险因素。本综述总结了基于患者手术标本、转基因动物和患者来源的诱导多能干细胞(hiPSC)的研究,以探讨室性心律失常和SCD可能的分子机制。离子通道重塑、Ca2+稳态异常和肌丝Ca2+敏感性增加可能导致动作电位时程(APD)改变、折返环路形成以及触发活动,如早期后除极(EAD)或延迟后除极(DAD),从而导致HCM患者发生室性心律失常。除了植入ICD外,以晚钠电流通道抑制剂和肌球蛋白抑制剂为代表的新型药物也为预防HCM相关心律失常提供了思路。早期HCM患者理想的SCD预防策略需要结合基因筛查、hiPSC-CM检测、机器学习和先进的心电图研究,从而实现个体化的SCD预防。