The effect of Perampanel on EEG spectral power and connectivity in patients with focal epilepsy.


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
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

2176-2183

Informations 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.

Auteurs

Jacopo Lanzone (J)

Rehabilitation Unit, FERB Onlus Hospital, Trescore Balneario, Italy; Deparment of Systems Medicine, Neuroscience, University of Rome Tor Vergata, Rome, Italy. Electronic address: jacopo.lanzone@gmail.com.

Lorenzo Ricci (L)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy.

Mario Tombini (M)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy.

Marilisa Boscarino (M)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy.

Oriano Mecarelli (O)

Department of Neurology and Psychiatry, "Sapienza" University of Rome, Italy.

Patrizia Pulitano (P)

Department of Neurology and Psychiatry, "Sapienza" University of Rome, Italy.

Vincenzo Di Lazzaro (V)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy.

Giovanni Assenza (G)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy.

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Classifications MeSH