Evidence map›Paper›PMID 41461105›Full record

ArticleJMIR research protocols2025

Gut Microbiota, Antipsychotics, and Metabolic Alterations in Children and Adolescents: Protocol for a Longitudinal Observational Study.

Marcela França Dias, Ana Paula de Alcântara Freitas, Suzana Figueiredo Collares, Renata Maria Silva Santos, Yago Jean de Almeida Nogueira, Antônio Márcio de Ávila Júnior, Tamires Coelho Martins, Paulo Marcos Brasil Rocha, Marco Aurélio Romano-Silva, Débora Marques de Miranda

Abstract read
In one paragraph

Article in JMIR research protocols, 2025. 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

10 authors.

Marcela França DiasScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-3542-5151
Ana Paula de Alcântara FreitasScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0009-0003-4938-5888
Suzana Figueiredo CollaresScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0009-0002-9719-8158
Renata Maria Silva SantosScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0001-5737-7712
Yago Jean de Almeida NogueiraScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0001-6215-4310
Antônio Márcio de Ávila JúniorScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0009-0001-7841-3927
Tamires Coelho MartinsScientific Research Program Molecular Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0009-0001-2544-0972
Paulo Marcos Brasil RochaDepartment of Mental Health, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0003-2314-8588
Marco Aurélio Romano-SilvaDepartment of Mental Health, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-6558-4639
Débora Marques de MirandaDepartment of Pediatrics, Universidade Federal de Minas Gerais, Av. Alfredo Balena 190, Room 114, Belo Horizonte, 30130-100, Brazil, 55 31-3409-9753.ORCID 0000-0002-7081-8401

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Over the past decade, numerous studies have emphasized the important role of gut microbiota (GM) in maintaining the body's homeostasis. Imbalances in GM have been linked to many dysfunctions, such as metabolic and neurodevelopmental disorders. GM can be influenced by many factors, among them the use of certain medications, such as second-generation antipsychotics (SGAs), and, in turn, act upon the endocrine, immune, and nervous systems. Despite the growing interest in the microbiota-gut-brain axis, significant gaps remain in our understanding of how SGAs affect GM and the host metabolic profile. Objective: This study aims to build on the current knowledge on the impact of SGAs on clinical parameters, microbial and metabolic profiles, and behavior of children and adolescents undergoing treatment with SGAs. Methods: This is a prospective longitudinal study, in which the effects of SGAs will be assessed before and 3 to 6 months after their introduction. An integrated approach will be used, encompassing clinical data (such as weight, lipid profile, and glucose levels); microbiome and metabolome analyses; emotional, behavioral, and sleep patterns (assessed through psychiatric scales); and dietary habits. Results: This project was funded in November 2023 and will start data collection in January 2026. It is expected to be completed in 2027. Conclusions: This study is expected to provide insights into the multidimensional effects of SGAs on children and adolescents, including clinical data, GM microbial profile, metabolism, and behavior. The findings may contribute to a better understanding of treatment impacts and provide information on more personalized therapeutic strategies.

Indexed as

Antipsychotic AgentsGastrointestinal MicrobiomeAdolescentChildFemaleHumansLongitudinal StudiesMaleMetabolomeObservational Studies as TopicProspective StudiesAntipsychotic Agentsgut microbiota-brain axismetabolomemicrobiomepsychiatric disorderssecond-generation antipsychotics

Identifiers

PMID41461105
PMCPMC12747660

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.