Holter electrocardiography findings in Fukuyama congenital muscular dystrophy

IF 2.8 4区 医学 Q2 CLINICAL NEUROLOGY Neuromuscular Disorders Pub Date : 2025-01-01 DOI:10.1016/j.nmd.2024.105273
Ryo Sugiyama , Eri Takeshita , Yuko Shimizu-Motohashi , Hirofumi Komaki
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Abstract

Fukuyama congenital muscular dystrophy (FCMD) is the second most common childhood-onset muscular dystrophy in Japan. However, only a few comprehensive studies have investigated cardiac complications associated with FCMD, with none on arrhythmias. The present study evaluated 78 Holter electrocardiograms from 15 patients with FCMD. No patient developed fatal arrhythmia complications, but older patients tended to have increased premature ventricular contractions (PVCs). Besides age, no risk factors were found to be associated with the presence or absence of PVCs. The average heart rate over 24 h tended to be higher in patients with FCMD than in healthy young people. Moreover, some time domain variables of heart rate variability tended to decrease from the early stages of the disease, suggesting that autonomic nervous system function might have been impaired prior to the appearance of PVCs. FCMD is a progressive disease, with affected patients suffering from increased rates of PVCs over time, which can reflect cardiac dysfunction.
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福山先天性肌营养不良症的动态心电图表现。
福山先天性肌营养不良症(FCMD)是日本第二常见的儿童期肌营养不良症。然而,只有少数全面的研究调查了与口蹄疫相关的心脏并发症,没有关于心律失常的研究。本研究评估了15例口蹄疫患者的78例动态心电图。没有患者出现致命性心律失常并发症,但老年患者倾向于室性早搏(室性早搏)增加。除年龄外,未发现与室性早搏存在与否相关的危险因素。口蹄疫患者24小时内的平均心率往往高于健康年轻人。此外,心率变异性的一些时域变量从疾病的早期阶段开始趋于下降,这表明自主神经系统功能可能在室性早搏出现之前就已经受损。口蹄疫是一种进行性疾病,受影响的患者随着时间的推移会出现室性早搏的发生率增加,这可能反映出心功能障碍。
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来源期刊
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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