Evidence map›Paper›PMID 42129363›Full record

ArticleScientific reports2026

Food-sensitized children with juvenile colorectal polyps exhibit a distinct mucosal and fecal microbial signature associated with inflammation.

Manuela Ilid, Julián Vaccaro, Belén Polo, Viviana Bernedo, Paula Borobia, Luciana Guzmán, Lorena Menendez, Anabella Zosi, Cecilia Zubirí, Marcela García and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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

15 authors.

Manuela IlidInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina.
Julián VaccaroInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina.
Belén PoloInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina.
Viviana BernedoServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Paula BorobiaServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Luciana GuzmánServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Lorena MenendezServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Anabella ZosiServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Cecilia ZubiríServicio de Gastroenterología, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Marcela GarcíaSala de Alergia, Hospital Interzonal de Agudos Especializado en Pediatría Sor María Ludovica, Calle 14 N° 1631, La Plata, Argentina.
Mónica M CollavinoInstituto de Botánica del Nordeste (IBONE) - [CCT NORDESTE] Centro Científico Tecnológico CONICET - Nordeste, Sargento Juan Bautista Cabral N° 2131, Corrientes, Argentina.
Guillermo H DocenaInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina.
Renata CurciarelloInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina.
Luis DiambraCentro de Endocrinología Experimental y Aplicada (CENEXA), Universidad Nacional de La Plata, CCT-La Plata, CONICET, Blvd. 120 N° 1459, B1904, La Plata, Argentina. ldiambra@gmail.com.
Cecilia I MugliaInstituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Departamento de Ciencias Biológicas, Universidad Nacional de La Plata, CCT-La Plata, CONICET, centro CICPBA asociado, Boulevard 120 N° 1489, 2°Piso, 1900, La Plata, Argentina. cmuglia@biol.unlp.edu.ar.

Funding

Agencia Nacional de Promoción Científica y Tecnológica, Argentina PICT-2020-SERIE A-02879CONICET 11220200100174CO
6 · The paper itself

Abstract

Juvenile colorectal polyps (JCP) are frequent in children and are associated with type 2 inflammation and local IgE synthesis. Our previous work showed that children with JCP in our cohort are sensitized to food allergens. Here, we characterized the bacterial microbiota in fecal samples from food-sensitized children with JCP (FSS) and healthy controls (CS), as well as in JCP tissues and surrounding control tissues (SCT), using 16S rRNA gene sequencing. Although sample richness was comparable across groups, community composition clearly separated fecal from tissue samples and distinguished FSS from CS. ANCOM-BC analysis revealed a distinct microbial profile in FSS, with significant enrichment of genera including Prevotella and Sutterella, and a corresponding reduction in Akkermansia, Veillonella, and several butyrate-producing taxa relative to the CS group. JCP were characterized by enrichment of genera previously associated with inflammatory conditions, including Escherichia, Fusobacterium, and Streptococcus, compared to CS and FSS samples. Notably Akkermansia-depleted in FSS compared to CS-was enriched in JCP when contrasted with FSS, highlighting differences between tissue and fecal microbial profiles across independent cohorts. When compared to the SCT group, JCP samples exhibited higher abundances of Blautia, Phocaeicola, and Dorea. These findings suggest that JCP are associated with a distinct microbial profile across multiple comparisons, whereas FSS is primarily defined by a relative depletion of taxa commonly linked to gut homeostasis. This study provides, to our knowledge, the first comprehensive characterization of the JCP-associated microbiota in food-sensitized pediatric patients, suggesting a potential link between microbial composition and allergic-type inflammation within the polyp microenvironment. Given the limited sample size, particularly for the SCT group, these findings should be considered exploratory.

Indexed as

Colonic PolypsFecesFood HypersensitivityGastrointestinal MicrobiomeInflammationIntestinal MucosaAdolescentBacteriaChildChild, PreschoolFemaleHumansMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16SDysbiosisFood sensitizationJuvenile colorectal polypsMicrobiotaType 2 inflammation

Identifiers

PMID42129363
PMCPMC13365372

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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.