Pegg Emily J, Taylor Jason R, Mohanraj Rajiv
Department of Neurology, Manchester Centre for Clinical Neurosciences, United Kingdom; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, United Kingdom.
Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, United Kingdom; Manchester Academic Health Sciences Centre, United Kingdom.
Epilepsy Behav. 2020 Nov;112:107427. doi: 10.1016/j.yebeh.2020.107427. Epub 2020 Sep 16.
Idiopathic generalized epilepsies (IGE) are characterized by generalized interictal epileptiform discharges (IEDs) on a normal background electroencephalography (EEG). However, the yield of IEDs can be low. Approximately 20% of patients with IGE fail to achieve seizure control with antiepileptic drug (AED) treatment. Currently, there are no reliable prognostic markers for early identification of drug-resistant epilepsy (DRE). We examined spectral power of the interictal EEG in patients with IGE and healthy controls, to identify potential diagnostic and prognostic biomarkers of IGE.
A 64-channel EEG was recorded under standard conditions in patients with well-controlled IGE (WC-IGE, n = 19), drug-resistant IGE (DR-IGE, n = 18), and age-matched controls (n = 20). After preprocessing, fast Fourier transform was performed to obtain 1D frequency spectra for each EEG channel. The 1D spectra (averaged over channels) and 2D topographic maps (averaged over canonical frequency bands) were computed for each participant. Power spectra in the 3 cohorts were compared using one-way analysis of variance (ANOVA), and power spectra images were compared using T-contrast tests. A post hoc analysis compared peak alpha power between the groups.
Compared with controls, participants with IGE had higher interictal EEG spectral power in the delta band in the midline central region, in the theta band in the midline, in the beta band over the left hemisphere, and in the gamma band over right hemisphere and left central regions. There were no differences in spectral power between cohorts with WC-IGE and DR-IGE. Peak alpha power was lower in WC-IGE and DR-IGE than controls.
Electroencephalography spectral power analysis could form part of a clinically useful diagnostic biomarker for IGE; however, it did not correlate with response to AED in this study.
特发性全身性癫痫(IGE)的特征是在正常背景脑电图(EEG)上出现全身性发作间期癫痫样放电(IED)。然而,IED的检出率可能较低。约20%的IGE患者使用抗癫痫药物(AED)治疗无法实现癫痫控制。目前,尚无可靠的预后标志物用于早期识别药物难治性癫痫(DRE)。我们研究了IGE患者和健康对照者发作间期EEG的频谱功率,以确定IGE潜在的诊断和预后生物标志物。
在标准条件下,对病情得到良好控制的IGE患者(WC-IGE,n = 19)、药物难治性IGE患者(DR-IGE,n = 18)和年龄匹配的对照者(n = 20)进行64导EEG记录。预处理后,进行快速傅里叶变换以获得每个EEG通道的一维频谱。计算每个参与者的一维频谱(通道平均)和二维地形图(标准频段平均)。使用单因素方差分析(ANOVA)比较三组的功率谱,使用T对比检验比较功率谱图像。事后分析比较了各组之间的α波峰值功率。
与对照组相比,IGE患者在中线中央区域的δ频段、中线的θ频段、左半球的β频段以及右半球和左中央区域的γ频段具有更高的发作间期EEG频谱功率。WC-IGE组和DR-IGE组之间的频谱功率没有差异。WC-IGE组和DR-IGE组的α波峰值功率低于对照组。
脑电图频谱功率分析可作为IGE临床有用诊断生物标志物的一部分;然而,在本研究中它与AED反应无关。