Evidence map›Paper›PMID 41062272›Full record

ArticleeNeuro2025

Automated Classification of Sleep-Wake States and Seizures in Mice.

Brandon J Harvey, Viktor J Olah, Lauren M Aiani, Lucie I Rosenberg, Danny J Lasky, Benjamin Moxon, Nigel P Pedersen

Abstract read
In one paragraph

Article in eNeuro, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. REST-a deep learning tool for automated mouse sleep stage classification.Sleep advances : a journal of the Sleep Research Society · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Brandon J HarveyGraduate Program in Neuroscience, Emory University, Atlanta, Georgia 30322.
Viktor J OlahDepartment of Cell Biology, Emory University, Atlanta, Georgia 30322.
Lauren M AianiDepartment of Genetics, Emory University School of Medicine, Atlanta, Georgia 30322.
Lucie I RosenbergDepartment of Neurology, University of California, Davis, Davis, California 95618.
Danny J LaskyDepartment of Neurology, University of California, Davis, Davis, California 95618.
Benjamin MoxonDepartment of Neurological Surgery, University of California, Davis, Davis, California 95618.
Nigel P PedersenDepartment of Neurology, University of California, Davis, Davis, California 95618 nppedersen@ucdavis.edu.

Funding

Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Control of the Hippocampal Formation by the Supramammillary Hypothalamus - Anatomy, Physiology and in a Model of Medial Temporal Lobe EpilepsyK08NS105929 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PEDERSEN, NIGEL PAUL · 2018 to 2023
$963k
Slow-Wave Sleep Enhancement to Treat Epilepsy and Its ComorbiditiesR01NS147124 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Nigel Paul Pedersen · 2026 to 2026
$548k
Sleep-Wake and Epilepsy Interactions in a Mouse Model of Temporal Lobe EpilepsR21NS122011 · NINDS · EMORY UNIVERSITY · PI PEDERSEN, NIGEL PAUL · 2021 to 2021
$430k
NIMH NIH HHS T32 MH112507NINDS NIH HHS K08 NS105929NINDS NIH HHS R01 NS147124NINDS NIH HHS R21 NS122011
6 · The paper itself

Abstract

Sleep-wake states bidirectionally interact with epilepsy and seizures, but the mechanisms are unknown. A barrier to comprehensive characterization and the study of mechanisms has been the difficulty of annotating large chronic recording datasets. To overcome this barrier, we sought to develop an automated method of classifying sleep-wake states, seizures, and the postictal state in mice ranging from controls to mice with severe epilepsy with accompanying background electroencephalographic (EEG) abnormalities. We utilized a large dataset of recordings, including electromyogram, EEG, and hippocampal local field potentials, from control and intra-amygdala kainic acid-treated mice. We found that an existing sleep-wake classifier performed poorly, even after retraining. A support vector machine, relying on typically used scoring parameters, also performed below our benchmark. We then trained and evaluated several multilayer neural network architectures and found that a bidirectional long short-term memory-based model performed best. This "Sleep-Wake and Ictal State Classifier" (SWISC) showed high agreement between ground-truth and classifier scores for all sleep and seizure states in an unseen and unlearned epileptic dataset (average agreement 96.41% ± SD 3.80%) and saline animals (97.77 ± 1.40%). Channel dropping showed that SWISC was primarily dependent on hippocampal signals yet still maintained good performance (∼90% agreement) with EEG alone, thereby expanding the classifier's applicability to other epilepsy datasets. SWISC enables the efficient combined scoring of sleep-wake and seizure states in mouse models of epilepsy and healthy controls, facilitating comprehensive and mechanistic studies of sleep-wake and biological rhythms in epilepsy.

Indexed as

EpilepsySeizuresSleepWakefulnessAnimalsDisease Models, AnimalElectroencephalographyElectromyographyHippocampusKainic AcidMaleMiceMice, Inbred C57BLNeural Networks, ComputerSupport Vector MachineKainic Acidepilepsymachine learningseizuressleepsleep–wake

Identifiers

PMID41062272
PMCPMC12562536

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.