Santoro Francesco, Mango Federica, Mallardi Adriana, D'Alessandro Damiano, Casavecchia Grazia, Gravina Matteo, Correale Michele, Brunetti Natale Daniele
Cardiology Unit, Department of Medical and Surgical Sciences, University of Foggia, 71122 Foggia, Italy.
Radiology Unit, University Polyclinic Hospital of Foggia, 71100 Foggia, Italy.
J Clin Med. 2023 May 10;12(10):3397. doi: 10.3390/jcm12103397.
Hypertrophic cardiomyopathy (HCM) is a cardiac muscle disorder characterized by generally asymmetric abnormal hypertrophy of the left ventricle without abnormal loading conditions (such as hypertension or valvular heart disease) accounting for the left ventricular wall thickness or mass. The incidence of sudden cardiac death (SCD) in HCM patients is about 1% yearly in adults, but it is far higher in adolescence. HCM is the most frequent cause of death in athletes in the Unites States of America. HCM is an autosomal-dominant genetic cardiomyopathy, and mutations in the genes encoding sarcomeric proteins are identified in 30-60% of cases. The presence of this genetic mutation carries more than 2-fold increased risk for all outcomes, including ventricular arrhythmias. Genetic and myocardial substrate, including fibrosis and intraventricular dispersion of conduction, ventricular hypertrophy and microvascular ischemia, increased myofilament calcium sensitivity and abnormal calcium handling, all play a role as arrhythmogenic determinants. Cardiac imaging studies provide important information for risk stratification. Transthoracic echocardiography can be helpful to evaluate left ventricular (LV) wall thickness, LV outflow-tract gradient and left atrial size. Additionally, cardiac magnetic resonance can evaluate the prevalence of late gadolinium enhancement, which when higher than 15% of LV mass is a prognostic maker of SCD. Age, family history of SCD, syncope and non-sustained ventricular tachycardia at Holter ECG have also been validated as independent prognostic markers of SCD. Arrhythmic risk stratification in HCM requires careful evaluation of several clinical aspects. Symptoms combined with electrocardiogram, cardiac imaging tools and genetic counselling are the modern cornerstone for proper risk stratification.
肥厚型心肌病(HCM)是一种心肌疾病,其特征通常为左心室不对称性异常肥厚,且不存在导致左心室壁厚度或质量增加的异常负荷情况(如高血压或瓣膜性心脏病)。HCM患者心脏性猝死(SCD)的年发生率在成年人中约为1%,但在青少年中要高得多。在美国,HCM是运动员最常见的死亡原因。HCM是一种常染色体显性遗传性心肌病,30%-60%的病例可检测到编码肌节蛋白的基因突变。这种基因突变会使包括室性心律失常在内的所有不良后果风险增加两倍以上。遗传因素和心肌基质,包括纤维化、心室内传导离散、心室肥厚和微血管缺血、肌丝钙敏感性增加以及钙处理异常,均作为致心律失常的决定因素发挥作用。心脏成像研究为危险分层提供重要信息。经胸超声心动图有助于评估左心室(LV)壁厚度、左心室流出道梯度和左心房大小。此外,心脏磁共振成像可评估钆延迟强化的发生率,当高于左心室质量的15%时,是SCD的预后指标。年龄、SCD家族史、晕厥以及动态心电图监测发现的非持续性室性心动过速也已被证实为SCD的独立预后标志物。HCM的心律失常危险分层需要仔细评估多个临床方面。症状结合心电图、心脏成像工具和遗传咨询是进行正确危险分层的现代基石。