Evidence map›Paper›PMID 39528720›Full record

ArticleCommunications biology2024

Circadian desynchrony in early life leads to enduring autistic-like behavioral changes in adulthood.

Abhishek Mishra, Hao Lin, Rubal Singla, Nam Le, Michael Oraebosi, Dong Liu, Ruifeng Cao

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Emerging genetics of sleep and circadian disorders.Current opinion in pediatrics · 2026
    Article
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  6. Review
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

7 authors.

Abhishek MishraDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN, 55812, USA.
Hao LinDepartment of Neuroscience and Cell Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Rubal SinglaDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN, 55812, USA.
Nam LeDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN, 55812, USA.
Michael OraebosiDepartment of Neuroscience and Cell Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.ORCID 0000-0002-2408-4697
Dong LiuDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN, 55812, USA.ORCID 0000-0001-8941-0812
Ruifeng CaoDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN, 55812, USA. ruifeng.cao@rutgers.edu.ORCID 0000-0001-5105-7726

Funding

Mammalian target of rapamycin signaling and the suprachiasmatic circadian clockR01NS118026 · NINDS · UNIVERSITY OF MINNESOTA · PI CAO, RUIFENG (RAY) · 2020 to 2024
$1.8M
Integrated stress response and the circadian clockR01GM143260 · NIGMS · UNIVERSITY OF MINNESOTA · PI CAO, RUIFENG (RAY) · 2022 to 2025
$1.4M
NIGMS NIH HHS R01 GM143260NINDS NIH HHS R01 NS118026U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review) GM143260U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review) NS118026
6 · The paper itself

Abstract

Circadian rhythm regulates a variety of biological processes in almost all living organisms. Modern lifestyles, e.g. transmeridian travel, night shift, light at night, etc., frequently disrupt people's regular sleep-wake cycles and create a misalignment (circadian desynchrony) between the natural environment and the endogenous body clock, and between different circadian oscillators within the body. The long-term consequences of circadian desynchrony on neurodevelopment and adult behavior remain elusive. Increasing clinical evidence supports a correlation between the disruption of the circadian system and neurodevelopmental disorders, such as autism spectrum disorders. Despite clinical correlations, experimental evidence is yet to establish a link between circadian disturbance in early life and adult behavioral changes. Here, using a "short day" (SD) mouse model, in which mice were exposed to an 8 h/8 h light/dark (LD) cycle mimicking a "shift work" schedule from gestation day 1 to postnatal day 21, we performed a battery of behavioral tests to assess changes in adult behaviors, including sociability, affective behaviors, stereotypy, cognition and locomotor functions. In contrast to the control mice kept in a 12 h/12 h LD cycle, the adult SD mice entrained to the 8 h/8 h LD cycle, but their free running rhythms remained normal in constant darkness. Interestingly, however, the SD mice displayed diminished sociability, a reduced preference for social novelty, excessive repetitive behaviors, and compromised cognitive functions, all of which resemble characteristics of autism-like behavioral alterations. In addition, the SD mice exhibited significant anxiety- and depressive-like behaviors and impaired motor functions. By western blotting and immunostaining analyses, hyperactivation of the mTORC1/S6K1 pathway was detected in multiple forebrain regions of SD mice. These findings underscore the enduring impact of early-life circadian disruption on neurochemical signaling and behavioral patterns into adulthood, highlighting a pivotal role for circadian regulation in neurodevelopment.

Indexed as

Autistic DisorderBehavior, AnimalCircadian RhythmAnimalsDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLPhotoperiodSocial Behavior

Identifiers

PMID39528720
PMCPMC11555041

What OpenQuestion holds

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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.