From the Center for Cardiovascular Genetics, Brown Foundation Institute of Molecular Medicine, Texas Heart Institute (A.J.M., Y.T., L.L., J.C., J.T.W., B.Y.C.), Biostatistics/Epidemiology/Research Design Component, Center for Clinical and Translational Sciences (M.H., M.H.R.), Department of Epidemiology, Human Genetics, and Environmental Sciences (M.H.R.), Division of Clinical and Translational Sciences (M.H.R.), and Department of Internal Medicine, University of Texas Health Science Center, Houston (M.H.R.); Institute of Cardiovascular Science, University College London, United Kingdom (P.S.); Department of Radiology, Johns Hopkins Hospital, Baltimore, MD (C.-Y.L.); Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison (D.A.B.); and Department of Medicine, Methodist DeBakey Heart and Vascular Center, Houston, TX (N.S.K., S.F.N.).
Circ Res. 2018 Apr 13;122(8):1109-1118. doi: 10.1161/CIRCRESAHA.117.312647. Epub 2018 Mar 14.
Hypertrophic cardiomyopathy (HCM) is a genetic paradigm of cardiac hypertrophy. Cardiac hypertrophy and interstitial fibrosis are important risk factors for sudden death and morbidity in HCM. Oxidative stress is implicated in the pathogenesis of cardiac hypertrophy and fibrosis. Treatment with antioxidant N-acetylcysteine (NAC) reverses cardiac hypertrophy and fibrosis in animal models of HCM.
To determine effect sizes of NAC on indices of cardiac hypertrophy and fibrosis in patients with established HCM.
HALT-HCM (Hypertrophy Regression With N-Acetylcysteine in Hypertrophic Cardiomyopathy) is a double-blind, randomized, sex-matched, placebo-controlled single-center pilot study in patients with HCM. Patients with HCM, who had a left ventricular wall thickness of ≥15 mm, were randomized either to a placebo or to NAC (1:2 ratio, respectively). NAC was titrated ≤2.4 g per day. Clinical evaluation, blood chemistry, and 6-minute walk test were performed every 3 months, and electrocardiography, echocardiography, and cardiac magnetic resonance imaging, the latter whenever not contraindicated, before and after 12 months of treatment. Eighty-five of 232 screened patients met the eligibility criteria, 42 agreed to participate; 29 were randomized to NAC and 13 to placebo groups. Demographic, echocardiographic, and cardiac magnetic resonance imaging phenotypes at the baseline between the 2 groups were similar. WSE in 38 patients identified a spectrum of 42 pathogenic variants in genes implicated in HCM in 26 participants. Twenty-four patients in the NAC group and 11 in the placebo group completed the study. Six severe adverse events occurred in the NAC group but were considered unrelated to NAC. The effect sizes of NAC on the clinical phenotype, echocardiographic, and cardiac magnetic resonance imaging indices of cardiac hypertrophy, function, and extent of late gadolinium enhancement-a surrogate for fibrosis-were small.
Treatment with NAC for 12 months had small effect sizes on indices of cardiac hypertrophy or fibrosis. The small sample size of the HALT-HCM study hinders from making firm conclusions about efficacy of NAC in HCM.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT01537926.
肥厚型心肌病(HCM)是一种心肌肥厚的遗传模式。心肌肥厚和间质纤维化是 HCM 患者发生猝死和发病的重要危险因素。氧化应激与心肌肥厚和纤维化的发病机制有关。在 HCM 的动物模型中,抗氧化剂 N-乙酰半胱氨酸(NAC)的治疗可逆转心肌肥厚和纤维化。
确定 NAC 对已确诊的 HCM 患者心肌肥厚和纤维化指标的作用大小。
HALT-HCM(肥厚型心肌病中 N-乙酰半胱氨酸的心肌肥厚消退)是一项双盲、随机、性别匹配、安慰剂对照的单中心 HCM 患者先导研究。HCM 患者的左心室壁厚度≥15mm,随机分为安慰剂或 NAC(1:2 比例)组。NAC 的滴定剂量≤2.4g/天。每 3 个月进行临床评估、血液化学检查和 6 分钟步行试验,治疗 12 个月前后进行心电图、超声心动图和心脏磁共振成像,后者在无禁忌症时进行。在 232 名筛查患者中,85 名符合入选标准,42 名同意参加;29 名被随机分配到 NAC 组,13 名被分配到安慰剂组。两组患者的人口统计学、超声心动图和心脏磁共振成像表型在基线时相似。在 38 名患者中,WSE 确定了 26 名参与者中 42 个与 HCM 相关的致病基因中的一个基因谱。NAC 组 24 名患者和安慰剂组 11 名患者完成了研究。NAC 组发生 6 例严重不良事件,但认为与 NAC 无关。NAC 治疗 12 个月对心肌肥厚、功能和晚期钆增强的临床表型、超声心动图和心脏磁共振成像指标(纤维化的替代指标)的作用大小较小。
NAC 治疗 12 个月对心肌肥厚或纤维化指标的作用大小较小。HALT-HCM 研究的样本量较小,无法对 NAC 在 HCM 中的疗效作出明确结论。