Evidence map›Paper›PMID 42739062›Full record

ReviewNutrients2026

The Adolescent Microbiome-Gut-Brain Axis: Development, Mechanisms, and Translational Perspectives.

Dolores B Vazquez-Sanroman, Liam Longaberger, Alondra Chance, Michael Anderson, Nedra Wilson, Gerwald Koehler

Abstract readReview
In one paragraph

Review in Nutrients, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Dolores B Vazquez-SanromanDepartment of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.ORCID 0000-0003-4786-3287
Liam LongabergerDepartment of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.
Alondra ChanceDepartment of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.
Michael AndersonDepartment of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.ORCID 0000-0002-1903-5735
Nedra WilsonDepartment of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.ORCID 0000-0001-7500-8996
Gerwald KoehlerDepartment of Biochemistry and Microbiology, Oklahoma State University Center for Health Sciences, 1111 W. 17 Street, Tulsa, OK 74107, USA.

Funding

The adolescent microbiome-gut-brain axis as a potential target in opioid abuse disordersP20GM152333 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI TYRRELL CONWAY · 2024 to 2026
$8.7M
NIGMS NIH HHS P20 GM152333NIH HHS 5P20GM152333-02
6 · The paper itself

Abstract

backgroundAdolescence represents a pivotal, yet understudied, developmental window in which maturation of the gut microbiome, neural circuits, endocrine systems, and behavioral processes converge. Although early-life microbiota-gut-brain interactions are well established, emerging evidence demonstrates that adolescence constitutes a "second sensitive period" during which microbial composition, metabolic output, and immune function undergo substantial restructuring. These microbial transitions parallel key neurodevelopmental events, including synaptic pruning, dopaminergic refinement, and heightened neuroendocrine activity, suggesting a coordinated microbiome-gut-brain developmental program. Cross-species comparisons reveal broad alignment between rodent and human adolescent milestones, though inconsistencies in development staging present challenges for translational interpretation. Environmental influences-such as diet, stress, antibiotics, and physical activity-further modulate microbial and neural maturation during this period, with potential long-term consequences for cognition, emotion, and stress responsivity. Mechanistically, microbial metabolites, vagal pathways, immune mediators, and steroid hormone interactions constitute key interfaces linking the gut microbiome to adolescent brain function. Recognizing adolescence as a mechanistically rich and plastic phase of gut-brain co-development underscores the need for harmonized methodological approaches and developmental alignment frameworks. METHODS-

resultsThis review synthesizes ontogenetic, mechanistic, and translational evidence to highlight conserved microbiome-gut-brain pathways and identifies opportunities for targeted interventions during this critical developmental stage.

Indexed as

Adolescent DevelopmentBrainGastrointestinal MicrobiomeAdolescentAnimalsGastrointestinal TractHumansNeurodevelopmentadolescencemicrobiome–gut–brain axisneurodevelopment

Identifiers

PMID42739062
PMCPMC13567016

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.