Evidence map›Paper›PMID 40244706›Full record

ArticleAnnals of clinical and translational neurology2025

Cortical Excitability Before and After Long-Term Perampanel Treatment for Epilepsy.

Robert M Helling, Johannes P van Dijk, Prisca R Bauer, Roland D Thijs, Josemir W Sander, Machiel Zwarts, Gerhard H Visser

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Robert M HellingStichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands.ORCID 0000-0003-0277-8484
Johannes P van DijkAcademic Center of Epileptology Kempenhaeghe, Heeze, the Netherlands.
Prisca R BauerInstitute of Musicians' Medicine, University Medical Center Freiburg, Freiburg im Breisgau, Germany.
Roland D ThijsStichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands.
Josemir W SanderStichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands.ORCID 0000-0001-6041-9661
Machiel ZwartsAcademic Center of Epileptology Kempenhaeghe, Heeze, the Netherlands.
Gerhard H VisserStichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands.

Funding

Eisai
6 · The paper itself

Abstract

objectiveAntiseizure medications (ASMs), which may influence cortical excitability, are the mainstay of epilepsy treatment. Transcranial magnetic stimulation (TMS) helps evaluate cortical excitability. We assessed changes in TMS responses using serial TMS measurements in people treated with an adjunctive noncompetitive AMPA-receptor antagonist.

methodsWe included adults with refractory, active epilepsy (≥ 1 seizure/month), advised to start adjunctive treatment with the noncompetitive AMPA-receptor antagonist perampanel as outpatients. After informed consent, we performed TMS measurement at three points: baseline before starting perampanel, at around 2 months after starting (4 mg/day), and at a final/effective dose around 6 months. Dependent on seizure reduction (> 50%), participants were dichotomized into responders (Rs) and nonresponders (NRs). We compared changes in motor cortex excitability through the rMT using a linear mixed-effects model. We evaluated TMS-evoked potentials (TEPs) to single pulse and paired pulse using within-subject Monte Carlo-based permutation analysis.

resultsWe included 18 adults, of whom 17 (6 R, 11 NR, 1 lost to follow-up) had baseline and second-month measurements, and nine (4 R, 5 NR) had all three. In responders, motor cortex excitability, quantified by rMT, significantly increased with increasing dose. Conversely, no significant changes were seen in the NR subgroup. TEPs for the single pulse and paired pulse showed no significant clusters for any peaks between measurement and group comparisons.

interpretationThe TEPs showed no significant changes between measurements and/or groups. Motor cortex excitability quantified by rMT is a potential biomarker to track or predict treatment outcomes in people starting adjunctive perampanel for epilepsy.

Indexed as

AnticonvulsantsCortical ExcitabilityDrug Resistant EpilepsyEvoked Potentials, MotorMotor CortexPyridonesAdultFemaleHumansMaleMiddle AgedNitrilesTranscranial Magnetic StimulationYoung AdultAnticonvulsantsNitrilesperampanelPyridonesAMPA‐receptor antagonistintracortical facilitationresting motor thresholdTMS‐evoked EEG potentialtranscranial magnetic stimulation

Identifiers

PMID40244706
PMCPMC12172129

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.