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利用发作间期颅内脑电图的兴奋性和抑制性活动作为致痫性的潜在生物标志物。

Utilizing Excitatory and Inhibitory Activity Derived from Interictal Intracranial Electroencephalography as Potential Biomarkers for Epileptogenicity.

机构信息

Department of Neurosurgery, The University of Tokyo.

Department of Neurosurgery, Jichi Medical University.

出版信息

Neurol Med Chir (Tokyo). 2024 Feb 15;64(2):65-70. doi: 10.2176/jns-nmc.2023-0207. Epub 2024 Jan 15.

Abstract

Epileptogenic zones (EZs), where epileptic seizures cease after resection, are localized by assessing the seizure-onset zone using ictal electroencephalography (EEG). Owing to the difficulty in capturing unpredictable seizures, biomarkers capable of identifying EZs from interictal EEG are anticipated. Recent studies using intracranial EEG have identified several potential candidate biomarkers for epileptogenicity. High-frequency oscillation (HFO) was initially expected to be a robust biomarker of abnormal excitatory activity in the ictogenic region. However, HFO-guided resection failed to improve seizure prognosis. Meanwhile, the regularity of low-gamma oscillations (30-80 Hz) indicates inhibitory interneurons' hypersynchronization, which could be used to localize the EZ. Besides resting-state EEG assessments, evoked potentials elicited by single-pulse electrical stimulation, such as corticocortical evoked potentials (CCEP), became valuable tools for assessing epileptogenic regions. CCEP responses recorded in the cortex remote from the stimulation site indicate functional connectivity, revealing increased internal connectivity within the ictogenic region and elevated inhibitory input from the non-involved regions to the ictogenic region. Conversely, large responses close to the stimulation site reflect local excitability, manifesting as an increased N1 amplitude and overriding HFO. Further research is required to establish whether these novel electrophysiological methods, either individually or in combination, can function as robust biomarkers of epileptogenicity and hold promise for improving seizure prognosis.

摘要

致痫区(EZs)是指癫痫发作停止后切除的区域,通过评估发作起始区来定位,方法是使用发作期脑电图(EEG)。由于难以捕捉不可预测的癫痫发作,因此需要能够从间期 EEG 中识别 EZs 的生物标志物。最近使用颅内 EEG 的研究已经确定了几个潜在的致痫性候选生物标志物。高频振荡(HFO)最初被期望成为致痫区异常兴奋性活动的有力生物标志物。然而,HFO 引导的切除未能改善癫痫预后。同时,低伽马振荡(30-80 Hz)的规律性表明抑制性中间神经元的过度同步化,这可以用来定位 EZ。除了静息状态 EEG 评估外,单脉冲电刺激诱发的诱发电位,如皮质间皮质诱发电位(CCEP),成为评估致痫区的有价值工具。在刺激部位远处皮层记录的 CCEP 反应表明功能连接,显示出致痫区内的内部连接增加,以及非参与区域对致痫区的抑制输入增加。相反,靠近刺激部位的大反应反映了局部兴奋性,表现为 N1 振幅增加和 HFO 抑制。需要进一步研究这些新的电生理方法是否可以单独或组合作为致痫性的有力生物标志物,并有望改善癫痫预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6268/10918453/c412c58c11ea/1349-8029-64-0065-g001.jpg

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