Periviita Vesa, Männikkö Roope, Jokela Manu, Sud Richa, Hanna Michael G, Udd Bjarne, Palmio Johanna
Department of Neurology, Tampere University Hospital, Tampere, Finland.
UCL Queen Square Institute of Neurology, Department of Neuromuscular Disease, London, UK.
Eur J Neurol. 2025 May;32(5):e70157. doi: 10.1111/ene.70157.
This study aimed to determine the role of five new rare SCN4A variants suspected to cause paramyotonia or myotonic disorder.
Ten patients from seven families underwent clinical, neurophysiological, imaging, and muscle biopsy examinations. Genetic studies were performed with targeted sequencing of all known myopathy genes. Functional changes resulting from these variants were studied with HEK293T cells, by using a whole-cell patch clamp.
Five SCN4A variants were identified: c.662 T > C p.(F221S), c.2143G > A p.(A715T), c.4352G > A p.(R1451H), c.3610 A > G p.(N1204D), and c.4255 T > C, p.(F1419L). Patients had exercise- and/or cold-induced myalgia, muscle stiffness or cramping, and varying degrees of muscle weakness. On examination, some but not all patients had percussion myotonia or findings compatible with paramyotonia. One patient with the A715T variant also had eyelid myotonia. The patient with the F221S variant had ptosis, weakness in hip flexion, and mild muscle hypertrophy in the calves. EMG showed myotonic discharges in all the patients examined except for the patient with N1204D. Electrophysiological exercise tests demonstrated results compatible with the Fournier pattern in six patients. All but the N1204D variant showed gain-of-function features upon functional expression.
The clinical and genetic findings suggested that all five variants were pathogenic, whereas functional data did not confirm association with myotonia for N1204D. Our results expand the mutational spectrum of the SCN4A gene. The reported variants should be considered in patients with paramyotonia, or in patients with exercise-induced myalgia or muscle cramping and who demonstrate myotonia in EMG.
本研究旨在确定5种新的罕见SCN4A变异体在疑似导致僵人综合征或肌强直障碍中的作用。
来自7个家庭的10名患者接受了临床、神经生理学、影像学和肌肉活检检查。对所有已知的肌病基因进行靶向测序以开展基因研究。利用全细胞膜片钳技术,在HEK293T细胞中研究这些变异体导致的功能变化。
鉴定出5种SCN4A变异体:c.662 T>C p.(F221S)、c.2143G>A p.(A715T)、c.4352G>A p.(R1451H)、c.3610 A>G p.(N1204D)和c.4255 T>C p.(F1419L)。患者有运动和/或寒冷诱发的肌痛、肌肉僵硬或痉挛,以及不同程度的肌无力。检查时,部分(但并非全部)患者有叩击性肌强直或符合僵人综合征的表现。1例携带A715T变异体的患者也有眼睑肌强直。携带F221S变异体的患者有上睑下垂症、髋部屈曲无力以及小腿轻度肌肉肥大。除携带N1204D变异体的患者外,所有接受检查的患者肌电图均显示肌强直放电。电生理运动试验结果显示6例患者符合富尼耶模式。除N1204D变异体外,所有变异体在功能表达时均表现出功能增强特征。
临床和基因研究结果表明,所有5种变异体均具有致病性,而功能数据未证实N1204D与肌强直有关联。我们的结果扩展了SCN4A基因的突变谱。对于僵人综合征患者,或运动诱发肌痛或肌肉痉挛且肌电图显示肌强直的患者,应考虑本文报道的变异体。