Cardiac Myosin Inhibitors as a Novel Treatment Option for Obstructive Hypertrophic Cardiomyopathy: Addressing the Core of the Matter

Ahmad Masri, I. Olivotto
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引用次数: 11

Abstract

mid- ventricular, and post- SRT phenotypes. Patients with heart failure with preserved ejection fraction also represent a future target for CMIs given their mechanism of action. Finally, in the minority of patients who present or progress to end- stage disease (defined as a left ventricular ejection fraction ≤50%), CMIs and SRT are contraindicated and/or not beneficial, and standard of care therapies are not typically effective. In these scenarios, advanced heart failure therapies are required. CMs indicates cardiac myosin inhibitors; G−, genotype negative; G+, genotype positive; HFpEF, heart failure with preserved ejection fraction; ICD, internal cardioverter defibrillator; LVAD, left ventricular assist device; nHCM, non- obstructive hypertrophic cardiomyopathy; NYHA, New Yok Heart Association; oHCM, obstructive hypertrophic cardiomyopathy; P−, phenotype negative; P+, phenotype positive; and SRT, septal reduction therapies.
心肌肌球蛋白抑制剂作为阻塞性肥厚性心肌病的新治疗选择:解决问题的核心
中心室和SRT后表型。考虑到cmi的作用机制,保留射血分数的心力衰竭患者也代表着cmi未来的目标。最后,在少数出现或进展为终末期疾病(定义为左室射血分数≤50%)的患者中,CMIs和SRT是禁忌和/或无效的,标准护理治疗通常无效。在这些情况下,需要先进的心力衰竭治疗。CMs表示心肌肌球蛋白抑制剂;G−,基因型阴性;G+,基因型阳性;HFpEF,保留射血分数的心力衰竭;ICD,内部转复除颤器;左心室辅助装置;nHCM,非阻塞性肥厚性心肌病;纽约心脏协会;oHCM,梗阻性肥厚性心肌病;P−,表型阴性;P+,表型阳性;和SRT,间隔缩小疗法。
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