Effect of interictal epileptiform discharges on EEG-based functional connectivity networks

被引:16
作者
Hu, Derek K. [1 ]
Mower, Andrew [2 ,3 ]
Shrey, Daniel W. [2 ,3 ]
Lopour, Beth A. [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[2] Childrens Hosp Orange Cty, Div Neurol, Orange, CA 92668 USA
[3] Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
关键词
Epilepsy; Infantile spasms; Electroencephalography; Functional connectivity; Interictal epileptiform discharges; Brain mapping; EPILEPSY; MODEL; SPIKES;
D O I
10.1016/j.clinph.2020.02.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Functional connectivity networks (FCNs) based on interictal electroencephalography (EEG) can identify pathological brain networks associated with epilepsy. FCNs are altered by interictal epileptiform discharges (IEDs), but it is unknown whether this is due to the morphology of the IED or the underlying pathological activity. Therefore, we characterized the impact of IEDs on the FCN through simulations and EEG analysis. Methods: We introduced simulated IEDs to sleep EEG recordings of eight healthy controls and analyzed the effect of IED amplitude and rate on the FCN. We then generated FCNs based on epochs with and without IEDs and compared them to the analogous FCNs from eight subjects with infantile spasms (IS), based on 1340 visually marked IEDs. Differences in network structure and strength were assessed. Results: IEDs in IS subjects caused increased connectivity strength but no change in network structure. In controls, simulated IEDs with physiological amplitudes and rates did not alter network strength or structure. Conclusions: Increases in connectivity strength in IS subjects are not artifacts caused by the interictal spike waveform and may be related to the underlying pathophysiology of IS. Significance: Dynamic changes in EEG-based FCNs during IEDs may be valuable for identification of pathological networks associated with epilepsy. (C) 2020 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1087 / 1098
页数:12
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