Stefanou Maria-Ioanna, Desideri Debora, Marquetand Justus, Belardinelli Paolo, Zrenner Christoph, Lerche Holger, Ziemann Ulf
Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, University of Tübingen, Hoppe-Seyler-Str. 3, 72076 Tübingen, Germany.
Department of Neurology & Epileptology, and Hertie Institute for Clinical Brain Research, University of Tübingen, Hoppe-Seyler-Str. 3, 72076 Tübingen, Germany.
Clin Neurophysiol. 2017 Dec;128(12):2503-2509. doi: 10.1016/j.clinph.2017.10.008. Epub 2017 Oct 20.
Mutations in STX1B encoding the presynaptic protein syntaxin-1B are associated with febrile seizures with or without epilepsy. It is unclear to what extent these mutations are linked to abnormalities of cortical glutamatergic or GABAergic neurotransmission. We explored this question using single- and paired-pulse transcranial magnetic stimulation (TMS) excitability markers.
We studied nine currently asymptomatic adult STX1B mutation carriers with history of epilepsy and febrile seizures, who had been seizure-free for at least eight years without antiepileptic drug treatment, and ten healthy age-matched controls. Resting motor threshold (RMT), and input-output curves of motor evoked potential (MEP) amplitude, short-interval intracortical inhibition (SICI, marker of GABAergic excitability) and intracortical facilitation (ICF, marker of glutamatergic excitability) were tested.
RMT, and input-output curves of MEP amplitude, SICI and ICF revealed no significant differences between STX1B mutation carriers and healthy controls.
Findings suggest normal motor cortical GABAergic and glutamatergic excitability in currently asymptomatic STX1B mutation carriers.
TMS measures of motor cortical excitability show utility in demonstrating normal excitability in adult STX1B mutation carriers with history of seizures.
编码突触前蛋白 syntaxin-1B 的 STX1B 基因突变与伴或不伴癫痫的热性惊厥相关。目前尚不清楚这些突变在多大程度上与皮质谷氨酸能或γ-氨基丁酸能神经传递异常有关。我们使用单脉冲和双脉冲经颅磁刺激(TMS)兴奋性标记物来探究这个问题。
我们研究了 9 名目前无症状的成年 STX1B 基因突变携带者,他们有癫痫和热性惊厥病史,在未接受抗癫痫药物治疗的情况下至少八年无癫痫发作,以及 10 名年龄匹配的健康对照者。测试了静息运动阈值(RMT)、运动诱发电位(MEP)幅度的输入-输出曲线、短间隔皮质内抑制(SICI,γ-氨基丁酸能兴奋性标记物)和皮质内易化(ICF,谷氨酸能兴奋性标记物)。
RMT 以及 MEP 幅度、SICI 和 ICF 的输入-输出曲线在 STX1B 基因突变携带者和健康对照者之间没有显著差异。
研究结果表明,目前无症状的 STX1B 基因突变携带者的运动皮质γ-氨基丁酸能和谷氨酸能兴奋性正常。
运动皮质兴奋性的 TMS 测量在证明有癫痫病史的成年 STX1B 基因突变携带者的兴奋性正常方面显示出实用性。