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肥厚型心肌病中的心肌肌球蛋白抑制剂

Cardiac myosin inhibitors in hypertrophic cardiomyopathy.

作者信息

Lim Jaehyun, Kim Hyung-Kwan

机构信息

Division of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Cardiovasc Imaging. 2025 Jul 7;33(1):7. doi: 10.1186/s44348-025-00052-7.

Abstract

Mavacamten, the first selective and reversible cardiac myosin inhibitor (CMI), has been introduced to the clinical arena for the treatment of obstructive hypertrophic cardiomyopathy (HCM). By reducing excessive actin-myosin cross-bridging, this agent decreases myocardial contractility and alleviates the dynamic left ventricular outflow tract (LVOT) obstruction in obstructive HCM. In the EXPLORER-HCM trial, mavacamten significantly improved exercise capacity, symptoms, and LVOT pressure gradients, while the VALOR-HCM trial proved it can obviate the need for septal reduction therapy in patients who were deemed to be candidates for septal reduction therapy. Notably, long-term data (MAVA-LTE study) has demonstrated sustained benefits up to 180 weeks, with < 10% experiencing transient reductions in left ventricular ejection fraction < 50% and only 1.3% of permanent discontinuation rate. Aficamten, a next-generation CMI with a shorter half-life, has also demonstrated comparable efficacy. Reverse remodeling following treatment was noted in both agents. In nonobstructive HCM, preliminary studies (MAVERICK-HCM trial and cohort 4 of REDWOOD-HCM trial) have reported improvements in cardiac serum biomarkers and symptoms. However, the preliminary results from phase 3 trials (ODYSSEY-HCM trial) revealed that primary endpoints were not met in nonobstructive HCM. Regarding safety, both were generally well tolerated. Although an LVEF reduction occurred in some patients, it was reversible with a dose reduction or a short-term drug cessation. These results emphasize careful dosing strategy with regular echocardiographic monitoring. Real-world data have also demonstrated consistent efficacy and safety across varying ethnic groups without new safety signals. CMI is a major advance in HCM management. However, future studies must provide data on hard clinical outcomes, such as heart failure hospitalization or death. Ongoing trials comparing CMI to traditional first-line therapies, such as β-blockers, will clarify their potential role as an initial therapeutic option.

摘要

马伐卡坦是首个选择性且可逆的心肌肌球蛋白抑制剂(CMI),已被引入临床用于治疗梗阻性肥厚型心肌病(HCM)。通过减少过多的肌动蛋白 - 肌球蛋白交叉桥联,该药物降低心肌收缩力,减轻梗阻性HCM患者的动态左心室流出道(LVOT)梗阻。在EXPLORER - HCM试验中,马伐卡坦显著改善了运动能力、症状以及LVOT压力梯度,而VALOR - HCM试验证明它可以使被认为适合进行室间隔减容治疗的患者无需进行该治疗。值得注意的是,长期数据(MAVA - LTE研究)显示长达180周都有持续益处,<10%的患者左心室射血分数短暂降至<50%,永久停药率仅为1.3%。阿菲卡坦是一种半衰期较短的下一代CMI,也显示出了相当的疗效。两种药物治疗后均观察到逆向重塑。在非梗阻性HCM中,初步研究(MAVERICK - HCM试验和REDWOOD - HCM试验队列4)报告了心脏血清生物标志物和症状有所改善。然而,3期试验(ODYSSEY - HCM试验)的初步结果显示非梗阻性HCM未达到主要终点。在安全性方面,两者总体耐受性良好。虽然一些患者出现了左心室射血分数降低,但通过减少剂量或短期停药是可逆的。这些结果强调了采用仔细的给药策略并定期进行超声心动图监测。真实世界数据也表明,在不同种族群体中,CMI具有一致的疗效和安全性,且没有新的安全信号。CMI是HCM管理方面的一项重大进展。然而,未来的研究必须提供关于心力衰竭住院或死亡等硬临床结局的数据。正在进行的将CMI与传统一线疗法(如β受体阻滞剂)进行比较的试验将阐明它们作为初始治疗选择的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f450/12232738/eab43c74e90f/44348_2025_52_Fig1_HTML.jpg

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