| Literature DB >> 33804412 |
Alessia Argirò1, Mattia Zampieri1, Martina Berteotti1, Alberto Marchi1, Luigi Tassetti1, Chiara Zocchi1, Luisa Iannone2, Beatrice Bacchi2, Francesco Cappelli1, Pierluigi Stefàno2, Niccolò Marchionni3, Iacopo Olivotto1.
Abstract
Hypertrophic cardiomyopathy (HCM) is a common myocardial disease characterized by otherwise unexplained left ventricular hypertrophy. The main cause of disabling symptoms in patients with HCM is left ventricular outflow tract (LVOT) obstruction. This phenomenon is multifactorial, determined both by anatomical and functional abnormalities: myocardial hypercontractility is believed to represent one of its major determinants. The anatomical anomalies are targeted by surgical interventions, whereas attenuating hypercontractility is the objective of old and new drugs including the novel class of allosteric myosin inhibitors. This review summarizes the current treatment modalities and discusses the emerging therapeutical opportunities focusing on the recently developed cardiac myosin ATPase inhibitors Mavacamten and CK-274. Novel surgical and interventional approaches are also discussed.Entities:
Keywords: hypertrophic cardiomyopathy; left ventricular outflow tract obstruction; mavacamten; septal reduction therapy
Year: 2021 PMID: 33804412 PMCID: PMC7957690 DOI: 10.3390/jcm10050951
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241