Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital, Okayama, Japan.
Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital, Okayama, Japan.
Epilepsy Res. 2024 May;202:107359. doi: 10.1016/j.eplepsyres.2024.107359. Epub 2024 Apr 4.
In developmental and epileptic encephalopathy with spike-and-wave activation in sleep (DEE-SWAS), the thalamocortical network is suggested to play an important role in the pathophysiology of the progression from focal epilepsy to DEE-SWAS. Ethosuximide (ESM) exerts effects by blocking T-type calcium channels in thalamic neurons. With the thalamocortical network in mind, we studied the prediction of ESM effectiveness in DEE-SWAS treatment using phase-amplitude coupling (PAC) analysis.
We retrospectively enrolled children with DEE-SWAS who had an electroencephalogram (EEG) recorded between January 2009 and September 2022 and were prescribed ESM at Okayama University Hospital. Only patients whose EEG showed continuous spike-and-wave during sleep were included. We extracted 5-min non-rapid eye movement sleep stage N2 segments from EEG recorded before starting ESM. We calculated the modulation index (MI) as the measure of PAC in pair combination comprising one of two fast oscillation types (gamma, 40-80 Hz; ripples, 80-150 Hz) and one of five slow-wave bands (delta, 0.5-1, 1-2, 2-3, and 3-4 Hz; theta, 4-8 Hz), and compared it between ESM responders and non-responders.
We identified 20 children with a diagnosis of DEE-SWAS who took ESM. Fifteen were ESM responders. Regarding gamma oscillations, significant differences were seen only in MI with 0.5-1 Hz slow waves in the frontal pole and occipital regions. Regarding ripples, ESM responders had significantly higher MI in coupling with all slow waves in the frontal pole region, 0.5-1, 3-4, and 4-8 Hz slow waves in the frontal region, 3-4 Hz slow waves in the parietal region, 0.5-1, 2-3, 3-4, and 4-8 Hz slow waves in the occipital region, and 3-4 Hz slow waves in the anterior-temporal region.
High MI in a wider area of the brain may represent the epileptic network mediated by the thalamus in DEE-SWAS and may be a predictor of ESM effectiveness.
在睡眠中出现棘慢波放电的发育性和癫痫性脑病(DEE-SWAS)中,丘脑皮质网络被认为在从局灶性癫痫发展为 DEE-SWAS 的病理生理学中发挥重要作用。乙琥胺(ESM)通过阻断丘脑神经元中的 T 型钙通道发挥作用。考虑到丘脑皮质网络,我们使用相位-振幅耦合(PAC)分析研究了 ESM 治疗 DEE-SWAS 效果的预测。
我们回顾性招募了 2009 年 1 月至 2022 年 9 月期间在冈山大学医院接受 ESM 治疗的 DEE-SWAS 患儿。仅纳入脑电图(EEG)显示睡眠中连续棘慢波的患者。我们从 ESM 开始前记录的非快速眼动睡眠阶段 N2 段中提取 5 分钟的非快速眼动睡眠。我们计算调制指数(MI)作为 PAC 的度量,该度量包含两种快振荡类型(伽马,40-80 Hz;涟漪,80-150 Hz)之一和五个慢波带(德尔塔,0.5-1、1-2、2-3 和 3-4 Hz;θ,4-8 Hz)之一之间的对组合。我们比较了 ESM 反应者和非反应者之间的 MI。
我们确定了 20 名被诊断为 DEE-SWAS 的儿童,他们服用了 ESM。15 名是 ESM 反应者。关于伽马振荡,仅在前额极和枕叶区域观察到与 0.5-1 Hz 慢波的 MI 存在显著差异。关于涟漪,额叶极区所有慢波、额叶区 0.5-1、3-4、4-8 Hz 慢波、顶叶区 3-4 Hz 慢波、枕叶区 0.5-1、2-3、3-4、4-8 Hz 慢波、前颞区 3-4 Hz 慢波的耦合中,ESM 反应者的 MI 显著升高。
大脑更广泛区域的高 MI 可能代表 DEE-SWAS 中由丘脑介导的癫痫网络,并且可能是 ESM 有效性的预测指标。