| NEUROBIOLOGY OF DISEASE | 卷:123 |
| Electrophysiological biomarkers of epileptogenicity after traumatic brain injury | |
| Review | |
| Perucca, Piero1,2,3,4  Smith, Gregory5  Santana-Gomez, Cesar6  Bragin, Anatol6  Staba, Richard6  | |
| [1] Monash Univ, Dept Neurosci, Cent Clin Sch, Melbourne, Australia | |
| [2] Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia | |
| [3] Alfred Hlth, Dept Neurol, Melbourne, Vic, Australia | |
| [4] Univ Melbourne, Melbourne Med Sch, Melbourne, Vic, Australia | |
| [5] UCLA, David Geffen Sch Med, Dept Neurosurg, Los Angeles, CA 90095 USA | |
| [6] UCLA, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA | |
| 关键词: Post-traumatic epilepsy; Traumatic brain injury; Epileptogenesis; Seizure; EEG; Electrophysiology; Biomarker; High-frequency oscillations; Repetitive HFOs and spikes; Sleep spindles; | |
| DOI : 10.1016/j.nbd.2018.06.002 | |
| 来源: Elsevier | |
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【 摘 要 】
Post-traumatic epilepsy is the architype of acquired epilepsies, wherein a brain insult initiates an epileptogenic process culminating in an unprovoked seizure after weeks, months or years. Identifying biomarkers of such process is a prerequisite for developing and implementing targeted therapies aimed at preventing the development of epilepsy. Currently, there are no validated electrophysiological biomarkers of post-traumatic epileptogenesis. Experimental EEG studies using the lateral fluid percussion injury model have identified three candidate biomarkers of post-traumatic epileptogenesis: pathological high-frequency oscillations (HFOs, 80-300 Hz); repetitive HFOs and spikes (rHFOSs); and reduction in sleep spindle duration and dominant frequency at the transition from stage III to rapid eye movement sleep. EEG studies in humans have yielded conflicting data; recent evidence suggests that epileptiform abnormalities detected acutely after traumatic brain injury carry a significantly increased risk of subsequent epilepsy. Well-designed studies are required to validate these promising findings, and ultimately establish whether there are post-traumatic electrophysiological features which can guide the development of 'antiepileptogenic' therapies.
【 授权许可】
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| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_nbd_2018_06_002.pdf | 2332KB |
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