The effect of Perampanel on EEG spectral power and connectivity in patients with focal epilepsy.
Adult
Aged
Anticonvulsants
/ administration & dosage
Brain
/ drug effects
Drug Therapy, Combination
Electroencephalography
/ drug effects
Epilepsies, Partial
/ diagnosis
Female
Humans
Longitudinal Studies
Male
Middle Aged
Nerve Net
/ drug effects
Nitriles
/ administration & dosage
Prospective Studies
Pyridones
/ administration & dosage
Treatment Outcome
EEG
Epilepsy
Perampanel
Pharmaco-EEG
qEEG
Journal
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
received:
17
01
2021
revised:
22
04
2021
accepted:
10
05
2021
pubmed:
21
7
2021
medline:
10
11
2021
entrez:
20
7
2021
Statut:
ppublish
Résumé
Quantitative Encephalography (qEEG) depicts synthetically the features of EEG signal and represents a promising tool in the assessment of neurophysiological changes brought about by Anti-Seizure Medications (ASMs). In this study we characterized qEEG alterations related to add-on therapy with Perampanel (PER). PER is the only ASM presenting a direct glutamatergic antagonism, hence the characterization of PER induced EEG changes could help to better understand its large spectrum of efficacy. We analysed standard-19 channel-EEG from 25 People with Epilepsy (PwE) both before (T0) and after (T1) the introduction of PER as add-on treatment. Normal values were obtained in 30 healthy controls (HC) matched for sex and age. EEGs were analysed using Matlab™ and the EEGlab and Brainstorm toolkits. We extracted spectral power and connectivity (Phase locking Value) of EEG signal and then compared these features between T0 and T1 and across groups (PwE, HC), we also evaluated the correlations with clinical features. PwE showed increased theta power (p = 0.036) after the introduction of PER but no significant change of EEG connectivity. We also found that PwE have reduced beta power (p = 0.012) and increased connectivity in delta (p = 0.013) and theta (p = 0.007) range as compared to HC, but no significant change was observed between T0 and T1 in PwE. Finally, we found that PwE classified as drug responders to PER have greater alpha power both at T0 and at T1 (p = 0.024) suggesting that this parameter may predict response to treatment. PER causes slight increase of theta activity and does not alter connectivity as assessed by standard EEG. Moreover, greater alpha power could be a good marker of response to PER therapy, and potentially ASM therapy in general. Our results corroborate the hypothesis that pharmaco-EEG is a viable tool to study neurophysiological changes induced by ASM. Additionally, our work highlights the role of alpha power as a marker of ASM therapeutic response.
Identifiants
pubmed: 34284253
pii: S1388-2457(21)00617-9
doi: 10.1016/j.clinph.2021.05.026
pii:
doi:
Substances chimiques
Anticonvulsants
0
Nitriles
0
Pyridones
0
perampanel
H821664NPK
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2176-2183Informations de copyright
Copyright © 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.