Aug 2026· Cardiology Discovery· Vol 6, pp. 210-220· 0 citations· 83 references
TL;DR
This review comprehensively summarizes current research regarding novel HCM treatment approaches—incorporating approved pharmaceuticals, preclinical findings, and clinical trial data—with the aim of facilitating continued development of HCM therapeutics.
Abstract
Hypertrophic cardiomyopathy (HCM) is a prevalent inherited cardiovascular disorder characterized by left ventricular hypertrophy and constitutes the leading cause of exercise-induced sudden cardiac death in young individuals. Conventional therapeutic strategies, such as the use of β-blockers, calcium channel blockers, and septal reduction therapy, focus largely on symptomatic relief and often exhibit limited clinical efficacy. Recent years have witnessed significant progress across multiple therapeutic domains, encompassing general clinical management, pharmacotherapy, gene therapy, and invasive interventions. Emerging treatment modalities, including cardiac myosin inhibitors, myocardial metabolic modulators, anti-fibrotic agents, gene therapies, and interventional procedures, have shown promising potential. Concurrently, exercise management guidelines for patients with HCM have undergone progressive liberalization. These therapeutic innovations, together with optimized exercise strategies, may improve symptoms, prolong survival, and enhance quality of life. This review comprehensively summarizes current research regarding novel HCM treatment approaches—incorporating approved pharmaceuticals, preclinical findings, and clinical trial data—with the aim of facilitating continued development of HCM therapeutics.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder, yet remains substantially underdiagnosed in clinical practice. Although current guidelines define HCM primarily based on left ventricular wall thickness, this approach alone does not capture the full spectrum of disease expression. Compreh...
Viktoria Höller, P. Zwetsloot, V. Santner et al.· Heart Failure Reviews· 0 citations
Introduction: Hypertrophic cardiomyopathy is a genetic disease characterized by left ventricular hypertrophy and, in some patients, left ventricular outflow tract obstruction. Mavacamten is a primary cardiac myosin inhibitor that reduces hypercontractility, decreases actin-myosin cross-bridge formation, and promotes mo...
Karen Jessica Pilatasig Bazurto, Millie Tiffani León Jiménez, Edison Humberto Ruiz Intriago et al.· Sage Sphere International Jo...· 0 citations
Heart failure with preserved ejection fraction (HFpEF) presents a major clinical and therapeutic challenge owing to its complex pathophysiology and pronounced clinical heterogeneity. While traditional empirical strategies targeting comorbidities offered limited success, recent advances in molecular, hemodynamic, and au...
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This systematic review outlines the overall research landscape of SIC, including pathological mechanisms, epidemiological profiles, updated diagnostic systems and innovative therapeutic strategies, as well as existing challenges and future research priorities.
Nai-Hong Zhang, Neng Wang, Jia-Wen He et al.· Frontiers in Cardiovascular...· 0 citations
Hypertrophic cardiomyopathy (HCM) is the most common genetically inherited cardiomyopathy, with a prevalence near 1 in 500. HCM manifests as the presence of left ventricular (LV)hypertrophy that cannot be explained by the hemodynamic conditions. The characteristic histological findings are myocyte disarray and fibrosis...
Akshaj Darbar, Anhadh Law, Megan Clemens et al.· International Journal of Cli...· 0 citations
Background/Objectives: Type 2 diabetes mellitus (T2DM) is a global epidemic strongly associated with an increased risk of heart failure, independent of coronary artery disease or hypertension. This condition, historically termed diabetic cardiomyopathy (DCM) and recently redefined as “diabetic myocardial disorder,” rem...
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