Department of Clinical and Experimental Medicine, Neurological Clinic, University of Pisa, Pisa, Italy.
Department of Translational Research and of New Surgical and Medical Technologies, University of Pisa, Pisa, Italy.
Epilepsia. 2021 May;62(5):1184-1192. doi: 10.1111/epi.16875. Epub 2021 Mar 18.
Markers of seizure recurrence are needed to personalize antiseizure medication (ASM) therapy. In the clinical practice, EEG features are considered to be related to the risk of seizure recurrence for genetic generalized epilepsies (GGE). However, to our knowledge, there are no studies analyzing systematically specific EEG features as indices of ASM efficacy in GGE. In this study, we aimed at identifying EEG indicators of ASM responsiveness in Juvenile Myoclonic Epilepsy (JME), which, among GGE, is characterized by specific electroclinical features.
We compared the features of prolonged ambulatory EEG (paEEG, 22 h of recording) of JME patients experiencing seizure recurrence within a year ("cases") after EEG recording, with those of patients with sustained seizure freedom for at least 1 year after EEG ("controls"). We included only EEG recordings of patients who had maintained the same ASM regimen (dosage and type) throughout the whole time period from the EEG recording up to the outcome events (which was seizure recurrence for the "cases", or 1-year seizure freedom for "controls"). As predictors, we evaluated the total number, frequency, mean and maximum duration of epileptiform discharges (EDs) and spike density (i.e. total EDs duration/artifact-free EEG duration) recorded during the paEEG. The same indexes were assessed also in standard EEG (stEEG), including activation methods.
Both the maximum length and the mean duration of EDs recorded during paEEG significantly differed between cases and controls; when combined in a binary logistic regression model, the maximum length of EDs emerged as the only valid predictor. A cut-off of EDs duration of 2.68 seconds discriminated between cases and controls with a 100% specificity and a 93% sensitivity. The same indexes collected during stEEG lacked both specificity and sensitivity.
The occurrence of prolonged EDs in EEG recording might represent an indicator of antiepileptic drug failure in JME patients.
需要有癫痫发作复发的标志物来实现个体化抗癫痫药物(ASM)治疗。在临床实践中,脑电图(EEG)特征被认为与遗传全面性癫痫(GGE)的癫痫复发风险有关。然而,据我们所知,目前尚无研究系统地分析特定 EEG 特征作为 GGE 中 ASM 疗效的指标。在这项研究中,我们旨在确定青少年肌阵挛性癫痫(JME)中 ASM 反应的 EEG 指标,在 GGE 中,JME 的特征是具有特定的电临床特征。
我们比较了 EEG 记录后一年内癫痫发作复发的 JME 患者(“病例”)与 EEG 记录后至少 1 年无癫痫发作的患者(“对照”)的长时间(22 小时)动态 EEG(paEEG)的特征。我们仅纳入在 EEG 记录至结果事件(“病例”为癫痫发作复发,“对照”为 1 年无癫痫发作)的整个时间段内始终保持相同 ASM 方案(剂量和类型)的患者的 EEG 记录。作为预测因子,我们评估了 paEEG 中记录的癫痫样放电(EDs)总数、频率、平均和最大持续时间,以及棘波密度(即总 EDs 持续时间/无伪迹 EEG 持续时间)。我们还评估了标准 EEG(stEEG)中的相同指标,包括激活方法。
paEEG 中记录的 EDs 的最大长度和平均持续时间在病例和对照组之间有显著差异;当将其结合到二元逻辑回归模型中时,EDs 的最大长度成为唯一有效的预测因子。EDs 持续时间为 2.68 秒的截断值可以将病例和对照组区分开来,特异性为 100%,敏感性为 93%。stEEG 中收集的相同指标既没有特异性也没有敏感性。
在 EEG 记录中出现延长的 EDs 可能是 JME 患者抗癫痫药物失败的一个指标。