Evidence map›Paper›PMID 39379558›Full record

ArticleScientific reports2024

Atypical gut microbiota composition in a mouse model of developmental stuttering.

Sayan Nanda, Bryan Lamot, Nicole Guarino, Evan Usler, Diane C Chugani, Aditya Dutta, Ho Ming Chow

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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.

Sayan NandaDepartment of Communication Sciences and Disorders, University of Delaware, Newark, DE, 19716, USA. snanda@udel.edu.
Bryan LamotDepartment of Animal and Food Sciences, University of Delaware, Newark, DE, 19716, USA.
Nicole GuarinoDepartment of Communication Sciences and Disorders, University of Delaware, Newark, DE, 19716, USA.
Evan UslerDepartment of Communication Sciences and Disorders, University of Delaware, Newark, DE, 19716, USA.
Diane C ChuganiDepartment of Communication Sciences and Disorders, University of Delaware, Newark, DE, 19716, USA.
Aditya DuttaDepartments of Animal and Food Sciences, Biological Sciences, Medical and Molecular Sciences, Microbiology Graduate Program, University of Delaware, Newark, DE, 19716, USA. adidutta@udel.edu.
Ho Ming ChowDepartment of Communication Sciences and Disorders, University of Delaware, Newark, DE, 19716, USA. hmc@udel.edu.

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Shawn W Polson · 2012 to 2026
$67.2M
Understanding synovial macrophage inflamm-aging within osteoarthritisP20GM139760 · NIGMS · UNIVERSITY OF DELAWARE · PI DAWN M ELLIOTT · 2021 to 2026
$19.1M
National Institute of General Medical Sciences, National Institutes of Health P20GM103446NIGMS NIH HHS P20 GM103446NIGMS NIH HHS P20 GM139760
6 · The paper itself

Abstract

Developmental stuttering is a complex neurodevelopmental disorder characterized by disfluent speech. It has been associated with mutations in genes involved in lysosomal enzyme trafficking. Mice with mutations in one such gene, Gnptab, exhibit atypical vocalizations analogous to stuttering in humans. This mouse model has enabled the study of various molecular mechanisms related to the disorder. Simultaneously, an increasing number of reports have suggested the role of gut microbiota in altered brain function and development in neurological disorders. In this study, we compared gut microbiota profiles from Gnptab mutant mice to wildtype control mice. Microbiome analysis demonstrated a distinct microbiota profile in Gnptab mutant mice. The most significant alteration was an increased relative abundance of Akkermansia, a genus of mucin degrading bacteria, which has previously been associated with multiple neurological disorders. Moreover, the altered microbiota profile of these mice was predicted to result in differences in abundance of several metabolic pathways, including short chain fatty acid and lipopolysaccharide synthesis. These pathways may play a role in the onset, progression and persistence of developmental stuttering. This is the first study to show a potential link between developmental stuttering and changes in the gut microbiota, laying the groundwork for a new research direction.

Indexed as

Disease Models, AnimalGastrointestinal MicrobiomeStutteringAkkermansiaAnimalsMaleMiceAkkermansiaDysbiosisFluency disordersLysosomal functionMetabolismMicrobiome

Identifiers

PMID39379558
PMCPMC11461706

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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.