Evidence map›Paper›PMID 40172341›Full record

ArticleCadernos de saude publica2025

Exploring the relationship between ultra-processed food consumption and gut microbiota at school age in a Brazilian birth cohort.

Etiene Dias Alves, Marina Xavier Carpena, Aluísio J D Barros, Elena M Comelli, Lorena López-Domínguez, Robert H J Bandsma, Iná da Silva Dos Santos, Alicia Matijasevich, Juliana Dos Santos Vaz, Romina Buffarini and 3 more

Abstract read
In one paragraph

Article in Cadernos de saude publica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

13 authors.

Etiene Dias AlvesUniversidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-1185-8972
Marina Xavier CarpenaUniversidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-4690-5791
Aluísio J D BarrosFaculdade de Medicina, Universidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-2022-8729
Elena M ComelliTemerty Faculty of Medicine, University of Toronto, Toronto, Canada.ORCID 0000-0002-5201-5437
Lorena López-DomínguezTemerty Faculty of Medicine, University of Toronto, Toronto, Canada.ORCID 0000-0002-5889-3986
Robert H J BandsmaTemerty Faculty of Medicine, University of Toronto, Toronto, Canada.ORCID 0000-0001-6358-4750
Iná da Silva Dos SantosFaculdade de Medicina, Universidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0003-1258-9249
Alicia MatijasevichFaculdade de Medicina, Universidade de São Paulo, São Paulo, Brasil.ORCID 0000-0003-0060-1589
Juliana Dos Santos VazFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-2880-767X
Romina BuffariniUniversidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-6905-8767
Isabel Oliveira BierhalsFaculdade de Medicina, Universidade de São Paulo, São Paulo, Brasil.ORCID 0000-0002-8739-8669
Maria Carolina BorgesUniversidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0001-7785-4547
Luciana Tovo-RodriguesFaculdade de Medicina, Universidade Federal de Pelotas, Pelotas, Brasil.ORCID 0000-0002-8732-6059

Funding

Wellcome Trust
6 · The paper itself

Abstract

Dietary patterns significantly impact health outcomes and gut microbiota composition. However, longitudinal studies associating ultra-processed food consumption with gut microbiota composition, especially among adolescents in low- and middle-income countries, are lacking. This study aimed to explore this association using data collected from 364 participants at ages 6, 11, and 12 years from the 2004 Pelotas (Brazil) Birth Cohort. Microbiota data was obtained at age 12 after 16S rRNA gene sequencing of self-collected fecal samples. Linear or logistic regression models evaluated the relationship between age groups and gut microbiota outcomes (alpha diversity, beta diversity and relative abundances at the phylum and genus levels), considering dietary covariates and demographic, socioeconomic, health-related, and behavioral factors. No significant associations between ultra-processed food consumption and alpha diversity were observed after multiple testing corrections, and there was no strong evidence linking ultra-processed food consumption and beta diversity, with unweighted metrics explaining little variance at ages 11 and 12. Nominal associations were found between ultra-processed food and relative abundances of Actinobacteria (p = 0.032) and Proteobacteria (p = 0.045) (phyla), Bacteroides (p = 0.037 at age 6; p = 0.015 at age 11) and Peptostreptococcus (p = 0.025 at age 6; p = 0.010 at age 11) (genera). However, these associations lost statistical significance after adjustments for multiple comparisons. These findings highlight the need for more longitudinal studies to better understand the complex interaction between ultra-processed food intake and gut microbiota composition in adolescent populations in low- and middle-income countries.

Indexed as

Fast FoodsGastrointestinal MicrobiomeBirth CohortBrazilChildFecesFemaleFood, ProcessedHumansLongitudinal StudiesMaleRNA, Ribosomal, 16SSocioeconomic FactorsRNA, Ribosomal, 16S

Identifiers

PMID40172341
PMCPMC11960759

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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.