Russo Vincenzo, Capolongo Antonio, Bottino Roberta, Carbone Andreina, Palladino Alberto, Liccardo Biagio, Nigro Gerardo, Marchel Michał, Golino Paolo, D'Andrea Antonello
Cardiology Unit, Department of Medical Translational Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80121 Naples, Italy.
Cardiomyology and Genetic Section, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
J Clin Med. 2023 Mar 1;12(5):1947. doi: 10.3390/jcm12051947.
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. Cardiac involvement is reported in 80% of cases and includes conduction disturbances, arrhythmias, subclinical diastolic and systolic dysfunction in the early stage of the disease; in contrast, severe ventricular systolic dysfunction occurs in the late stage of the disease. Echocardiography is recommended at the time of diagnosis with periodic revaluation in DM1 patients, regardless of the presence or absence of symptoms. Data regarding the echocardiographic findings in DM1 patients are few and conflicting. This narrative review aimed to describe the echocardiographic features of DM1 patients and their prognostic role as predictors of cardiac arrhythmias and sudden death.
1型强直性肌营养不良(DM1)是成人中最常见的肌肉营养不良症。据报道,80%的病例存在心脏受累,包括传导障碍、心律失常、疾病早期的亚临床舒张期和收缩期功能障碍;相比之下,严重的心室收缩功能障碍发生在疾病晚期。建议在诊断时对DM1患者进行超声心动图检查,并定期重新评估,无论有无症状。关于DM1患者超声心动图检查结果的数据很少且相互矛盾。本叙述性综述旨在描述DM1患者的超声心动图特征及其作为心律失常和猝死预测指标的预后作用。