Evidence map›Paper›PMID 41616664›Full record

ArticleEpilepsy & behavior : E&B2026

Cenobamate's effect on mood and seizure frequency.

Mert Karatas, Alperan Yavuz, Blake Newman, Angela Peters, Brian Johnson, Sindhu Richards, Pawan Rawal, Adrian Rothenfluh, Amir Arain

Abstract read
In one paragraph

Article in Epilepsy & behavior : E&B, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mert KaratasDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA; Molecular Medicine Program, University of Utah, Salt Lake City, UT 84112, USA. Electronic address: mert.karatas@utah.edu.
Alperan YavuzDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.
Blake NewmanDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.
Angela PetersDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.
Brian JohnsonDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.
Sindhu RichardsDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.
Pawan RawalDepartment of Neurology, University of Tennessee, Memphis, TN 38163, USA.
Adrian RothenfluhMolecular Medicine Program, University of Utah, Salt Lake City, UT 84112, USA; Department of Psychiatry, Huntsman Mental Health Institute, University of Utah, Salt Lake City, UT 84108, USA; Department of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA; Department of Neurobiology, University of Utah, Salt Lake City, UT 84112, USA.
Amir ArainDepartment of Neurology, University of Utah, Salt Lake City, UT 84132, USA.

Funding

Control of Alcohol Responses by Actin-Regulating GenesR01AA019526 · NIAAA · UT SOUTHWESTERN MEDICAL CENTER · PI ROTHENFLUH, ADRIAN · 2010 to 2025
$5.4M
Sleep Deficits induced by AlcoholR01AA031887 · NIAAA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Adrian Rothenfluh · 2025 to 2026
$1.1M
Mechanisms of psychostimulant-sleep interactionsR01DA061298 · NIDA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Adrian Rothenfluh · 2025 to 2026
$919k
Alcohol Tolerance as a Driver of Self-AdministrationR21AA031795 · NIAAA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI ROTHENFLUH, ADRIAN · 2024 to 2025
$405k
Genetics of Amphetamine PreferenceR21DA060453 · NIDA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI ROTHENFLUH, ADRIAN · 2024 to 2025
$383k
NIAAA NIH HHS R01 AA019526NIAAA NIH HHS R01 AA031887NIAAA NIH HHS R21 AA031795NIDA NIH HHS R01 DA061298NIDA NIH HHS R21 DA060453
6 · The paper itself

Abstract

objectiveReal-world experience with efficacy and tolerability of newly approved antiseizure medications (ASM) often diverges from findings in their controlled clinical trials. Cenobamate (CNB), demonstrated a high responder rate and seizure freedom in placebo-controlled trials. Since 40% of patients with epilepsy (PWE) experience comorbid depression, understanding the potential mood-related effects of CNB is critical. This retrospective study evaluates the impact of CNB on mood, tolerability, and seizure control when used as adjunctive therapy at our institution.

methodsA single-center retrospective chart review was conducted of adult patients with refractory focal epilepsy who initiated CNB add-on therapy (May 2020-July 2023). We assessed changes in depressive symptoms and seizure frequency. Eligibility required ≥3 months on CNB, seizure frequency available at baseline and last follow-up (events/30 days), and paired Patient Health Questionnaire-9 (PHQ-9) scores. Seizure outcomes were analyzed as paired change (ΔSeizures), as log

results73 adult PWE met study criteria. Median seizure frequency fell from 5 at baseline to 1.5 per 30 days at the last follow-up (p < 0.001), with a 50% median reduction (95% CI: 70%-19%) in seizure frequency within a median of 488 days of follow-up. At the last follow-up, 29% of patients were seizure-free overall. PHQ-9 scores did not worsen (median ΔPHQ-9 = 0 (HL = 0; 95% CI -2 to 0; 0.34), and in multiple linear regressions of ΔPHQ-9, no prespecified covariates were associated with mood outcomes.

conclusionOur findings suggest that CNB is a safe and effective adjunctive ASM that improves seizure control in PWE and that does not significantly change PHQ-9 scores. While better seizure control may mask the drug's potential effects on mood-as reduced seizure burden itself could influence depressive symptoms-its impact on individual mood was variable. These results highlight the need for further research. SIMPLE LANGUAGE SUMMARY: Patients with epilepsy often experience depression, making it important to assess whether new antiseizure medications affect mood. This study reviewed medical records of patients prescribed cenobamate (Xcopri) between May 2020 and August 2023. The results showed that cenobamate helped improve seizure control, and most patients did not experience a worsening of mood. These findings suggest that cenobamate is a safe option for epilepsy treatment, although further research is needed.

Indexed as

AffectAnticonvulsantsCarbamatesChlorophenolsDepressionDrug Resistant EpilepsyEpilepsies, PartialSeizuresTetrazolesAdultFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAnticonvulsantsCarbamatesCenobamateChlorophenolsTetrazolesCenobamateMoodPsychiatric comorbidities of epilepsyTreatment-resistant epilepsy

Identifiers

PMID41616664
PMCPMC13369269

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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.