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奥米卡替明在收缩性心力衰竭中的应用:一种新型肌球蛋白激活正性肌力药物的临床疗效及未来方向

Omecamtiv Mecarbil in Systolic Heart Failure: Clinical Efficacy and Future Directions of a Novel Myosin-Activating Inotropic Agent.

作者信息

Ramadan Mahmoud M, Alshawi Abdullah L, Mostafa Yasmeen A, Al-Obeid Mohammad T, Elmahal Mohammed

机构信息

Cardiology, Faculty of Medicine, Mansoura University, Mansoura, EGY.

Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, ARE.

出版信息

Cureus. 2025 Apr 12;17(4):e82128. doi: 10.7759/cureus.82128. eCollection 2025 Apr.

Abstract

Heart failure with reduced ejection fraction (HFrEF) remains a global health challenge, associated with high morbidity, mortality, and rising healthcare costs. Despite advances in guideline-directed therapy, many patients, especially those with severely reduced ejection fraction, remain symptomatic. Traditional inotropes, including β-agonists and phosphodiesterase inhibitors, are limited in chronic HFrEF due to risks of arrhythmias, calcium overload, and increased myocardial oxygen demand. Omecamtiv mecarbil (OM) is a novel cardiac myosin activator that enhances systolic contraction by increasing the efficiency of actin-myosin interactions. It prolongs systolic ejection time and improves stroke volume without elevating intracellular calcium or energy consumption. Although theoretical concerns exist regarding impaired diastolic filling, clinical trials have not confirmed such adverse effects in most patients. This narrative review discusses OM's pharmacologic profile, clinical trial data, and its potential as an adjunct therapy in advanced HFrEF. While not yet guideline-recommended, OM may benefit patients who remain symptomatic despite optimal treatment.

摘要

射血分数降低的心力衰竭(HFrEF)仍然是一项全球性的健康挑战,与高发病率、高死亡率以及不断上升的医疗成本相关。尽管在指南指导的治疗方面取得了进展,但许多患者,尤其是那些射血分数严重降低的患者,仍然有症状。传统的正性肌力药物,包括β受体激动剂和磷酸二酯酶抑制剂,由于存在心律失常、钙超载和心肌氧需求增加的风险,在慢性HFrEF中受到限制。奥米卡替麦卡比(OM)是一种新型的心肌肌球蛋白激活剂,通过提高肌动蛋白-肌球蛋白相互作用的效率来增强收缩期收缩。它延长收缩期射血时间并增加每搏输出量,而不会升高细胞内钙或增加能量消耗。尽管存在关于舒张期充盈受损的理论担忧,但临床试验尚未在大多数患者中证实此类不良反应。这篇叙述性综述讨论了OM的药理学特性、临床试验数据及其作为晚期HFrEF辅助治疗的潜力。虽然尚未得到指南推荐,但OM可能会使尽管接受了最佳治疗仍有症状的患者受益。

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