Olivotto Iacopo, Hellawell Jennifer L, Farzaneh-Far Ramin, Blair Christiana, Coppini Raffaele, Myers Jonathan, Belardinelli Luiz, Maron Martin S
From the Referral Center for Cardiomyopathies, Careggi University Hospital, Florence, Italy (I.O.); Gilead Sciences, Inc, Foster City, CA (J.L.H., R.F.-F., C.B., L.B.); Department of Preclinical and Clinical Pharmacology and Center of Molecular Medicine, University of Florence, Florence, Italy (R.C.); Veterans Affairs Palo Alto Health Care System and Stanford University, Palo Alto, CA (J.M.); and Hypertrophic Cardiomyopathy Center, Division of Cardiology, Tufts Medical Center, Boston, MA (M.S.M.).
Circ Heart Fail. 2016 Mar;9(3):e002764. doi: 10.1161/CIRCHEARTFAILURE.115.002764.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder, with an overall prevalence of at least 1:500 in the adult population although only a fraction of affected patients come to clinical recognition. It is also the most common cause of sudden cardiac death in young adults and a major cause of morbidity caused by chronic heart failure symptoms. However, more than half a century since the original description of the disease, there is no currently approved therapy for the treatment of patients with HCM, and to date there have been only 5 randomized studies of medical therapies in HCM. As such, unmet medical need in HCM has been highlighted by the National Heart, Lung, and Blood Institute (NHLBI) as a research priority. Encouragingly, the infrastructure needed to conduct rigorous clinical trials in HCM has recently emerged because of the heightened awareness and understanding of the disease, development of clinical centers of excellence, and advances in diagnostic imaging. In this article, we will discuss the complex pathophysiology of HCM, review the current therapeutic landscape, describe new mechanistic insights into the central role of the late sodium current in HCM, and introduce the scientific rationale and execution of the Impact of Late Sodium Current Inhibition on Exercise Capacity in Subjects with Symptomatic Hypertrophic Cardiomyopathy (LIBERTY-HCM) trial, the largest randomized, double-blind, placebo controlled clinical trial, now underway, designed to evaluate the effect of a novel pharmacological approach in patients with symptomatic HCM.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT02291237.
肥厚型心肌病(HCM)是最常见的遗传性心脏疾病,在成年人群中的总体患病率至少为1:500,尽管只有一小部分受影响的患者得到临床诊断。它也是年轻成年人心脏性猝死的最常见原因,以及慢性心力衰竭症状导致发病的主要原因。然而,自该疾病最初被描述以来已过去半个多世纪,目前尚无获批用于治疗HCM患者的疗法,迄今为止,关于HCM药物治疗的随机研究仅有5项。因此,美国国立心肺血液研究所(NHLBI)已将HCM未满足的医疗需求列为研究重点。令人鼓舞的是,由于对该疾病的认识和理解不断提高、卓越临床中心的发展以及诊断成像技术的进步,最近已出现了在HCM中开展严格临床试验所需的基础设施。在本文中,我们将讨论HCM复杂的病理生理学,回顾当前的治疗现状,描述关于晚钠电流在HCM中的核心作用的新机制见解,并介绍晚钠电流抑制对有症状肥厚型心肌病患者运动能力影响(LIBERTY-HCM)试验的科学原理和实施情况,这是目前正在进行的最大规模的随机、双盲、安慰剂对照临床试验,旨在评估一种新型药理学方法对有症状HCM患者的疗效。