Evidence map›Paper›PMID 41408339›Full record

ArticleMolecular autism2025

Dim light at night disrupts the sleep-wake cycle and exacerbates abnormal EEG activity in Cntnap2 knockout mice: implications for autism spectrum disorders.

Yumeng Wang, Ketema N Paul, Gene D Block, Tom Deboer, Christopher S Colwell

Abstract read
In one paragraph

Article in Molecular autism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Metaplastic sleep regulation inbioRxiv : the preprint server for biology · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Yumeng WangDepartment of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA, USA.
Ketema N PaulDepartment of Integrative Biology and Physiology, University of California Los Angeles, Los Angeles, CA, USA.
Gene D BlockDepartment of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA, USA.
Tom DeboerLaboratory for Neurophysiology, Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.
Christopher S ColwellDepartment of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA, USA. ccolwell@mednet.ucla.edu.

Funding

UCLA IDDRC: Translational CoreP50HD103557 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peyman Golshani, SUMA JACOB · 2020 to 2026
$9.6M
UCLA Center for Translational Research in Neurodevelopment: UC-TRaNU54HD087101 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BOOKHEIMER, SUSAN Y · 2016 to 2020
$6.5M
Eunice Kennedy Shriver National Institute of Child Health and Human Development P50HD103557NICHD NIH HHS P50 HD103557NICHD NIH HHS U54 HD087101UCLA 441587-GB-19933
6 · The paper itself

Abstract

backgroundEpilepsy is a common comorbidity in individuals with autism spectrum disorders (ASDs). Many patients with epilepsy as well as ASD experience disruptions in their sleep-wake cycle and daily fluctuations in symptom severity. Chronic exposure to light at nighttime can disrupt sleep and circadian rhythms. Contactin associated protein-like 2 knockout (Cntnap2 KO) mice, a model of ASD and epilepsy, exhibit sleep and circadian disturbances and abnormal events in the electroencephalogram (EEG). Here, we investigated how chronic dim light at night (DLaN) exposure affects sleep architecture, EEG power spectra, and abnormal EEG events in Cntnap2 KO and wildtype (WT) mice.

methodsMale and female Cntnap2 KO and WT mice were exposed to DLaN (5 lx) for 6 weeks. EEG recordings were collected and analyzed to assess sleep architecture, spectral power, and abnormal EEG events. A two-way repeated-measures analysis of variance (ANOVA) was used to evaluate the effects of DLaN across time and EEG frequencies, followed by Bonferroni-corrected post hoc tests where appropriate.

resultsDLaN exposure delayed wake onset and disrupted sleep patterns in a sex-dependent manner, with females being more affected. DLaN significantly increased slow-wave activity (SWA, 0.5–4 Hz) in both WT and KO mice, consistent with increased sleep pressure. Notably, DLaN markedly elevated the frequency of abnormal hypersynchronized EEG events in Cntnap2 KO mice and even induced such events in WT mice. Spectral analysis of abnormal EEG events revealed elevated theta power, suggesting hippocampal involvement.

conclusionsChronic DLaN exposure disrupts sleep architecture in a sex-dependent fashion and increases the occurrence of abnormal EEG events in Cntnap2 KO mice. These findings highlight the potential risks of nighttime light exposure for individuals with ASD and epilepsy, underscoring the importance of managing light environments to improve sleep quality and neurological health.

Indexed as

Autism Spectrum DisorderCircadian RhythmElectroencephalographyLightMembrane ProteinsNerve Tissue ProteinsSleepWakefulnessAnimalsDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLMice, KnockoutCNTNAP2 protein, mouseMembrane ProteinsNerve Tissue ProteinsAutism spectrum disorderDim light at nightEpilepsyMiceSeizureSex differenceSleep-wake rhythm

Identifiers

PMID41408339
PMCPMC12713241

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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.