Evidence map›Paper›PMID 40753218›Full record

ArticleJournal of neurodevelopmental disorders2025

Autism-like phenotype across the lifespan of Shank3B-mutant mice of both sexes.

Jakub Szabó, Johan Filo, Rebeka Démuthová, Emese Renczés, Veronika Borbélyová, Daniela Ostatníková, Peter Celec

Abstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2025. 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

7 authors.

Jakub SzabóInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Johan FiloInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Rebeka DémuthováInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Emese RenczésInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Veronika BorbélyováInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Daniela OstatníkováInstitute of Physiology, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Peter CelecInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia. peter.celec@imbm.sk.

Funding

Agentúra na Podporu Výskumu a Vývoja APVV-20-0070Agentúra na Podporu Výskumu a Vývoja APVV-20-0185Kultúrna a Edukacná Grantová Agentúra MŠVVaŠ SR 045UK-4/2020Vedecká Grantová Agentúra MŠVVaŠ SR a SAV 1/0635/20
6 · The paper itself

Abstract

backgroundHigh heritability (80-90%) of the autism spectrum disorder (ASD) and sex-biased incidence (3-4 times more boys than girls) suggest the roles of genetic predisposition and sex in the etiopathogenesis of the disorder. As ASD is commonly diagnosed in early childhood, most of the research is focused on children, yet animal research predominantly uses adult-aged animals. The effect of aging on the core and secondary ASD symptomatology is understudied, both in patients and animal models of ASD.

methodsTo investigate the effect of aging on sociability, repetitive behavior, exploration, locomotor activity, anxiety-like behavior, and object-avoidance behavior, behavioral phenotyping was conducted in Shank3B

resultsSocial deficits were observed only in old Shank3B

conclusionsPresent study shows that aging affects ASD-like phenotype in the Shank3B-mutant mouse model, even though the effect size seems to be small. The mechanisms underlying these partially sex-specific effects should be the subject of further research with potential translational implications.

Indexed as

AgingAutism Spectrum DisorderBehavior, AnimalNerve Tissue ProteinsSocial BehaviorAnimalsAnxietyDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLMice, KnockoutMicrofilament ProteinsPhenotypeSex FactorsMicrofilament ProteinsNerve Tissue ProteinsShank3 protein, mouseAnimal modelPhelan-McDermid syndromePhenotypingSymptom development

Identifiers

PMID40753218
PMCPMC12317579

What OpenQuestion holds

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Registered trials

None linked

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.