Evidence map›Paper›PMID 40288637›Full record

ArticleMolecular metabolism2025

Effects of children's microbiota on adipose and intestinal development in sex-matched mice persist into adulthood following a single fecal microbiota transplantation.

Federica La Rosa, Maria Angela Guzzardi, Mercedes Pardo-Tendero, Monica Barone, Chiara Ruocco, Gabriele Conti, Daniele Panetta, Daria Riabitch, Silvia Bernardi, Assuero Giorgetti and 5 more

Abstract read
In one paragraph

Article in Molecular metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Functional PET imaging of gut microbiota with [European journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Article
  3. Review
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.

Federica La RosaInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: federica.larosa@cnr.it.
Maria Angela GuzzardiInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: mariaangela.guzzardi@cnr.it.
Mercedes Pardo-TenderoDepartment of Pathology, University of Valencia, Health Research Institute INCLIVA/CIBERFES for Frailty and Healthy Aging, Blasco Ibañez, 15, 46010, Valencia, Spain. Electronic address: M.Mercedes.Pardo@uv.es.
Monica BaroneHuman Microbiomics Unit, Department of Medical and Surgical Sciences, University of Bologna, via Massarenti 9, 40138 Bologna Italy. Electronic address: monica.barone@unibo.it.
Chiara RuoccoCenter of Study and Research on Obesity, Department of Medical Biotechnology and Translational Medicine, University of Milan, via Vanvitelli 32, 20129 Milan, Italy. Electronic address: chiara.ruocco@unimi.it.
Gabriele ContiHuman Microbiomics Unit, Department of Medical and Surgical Sciences, University of Bologna, via Massarenti 9, 40138 Bologna Italy. Electronic address: gabriele.conti12@unibo.it.
Daniele PanettaInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: daniele.panetta@cnr.it.
Daria RiabitchInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: dariariabitch@cnr.it.
Silvia BernardiInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: silvia.bernardi@cnr.it.
Assuero GiorgettiFondazione Toscana Gabriele Monasterio, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: asso@ftgm.it.
Daniela CampaniDepartment of Surgical, Medical, Molecular Pathology and Critical Care Medicine, Division of Pathology, Pisa University Hospital, 56124 Pisa, Italy. Electronic address: daniela.campani@med.unipi.it.
Daniel MonleonDepartment of Pathology, University of Valencia, Health Research Institute INCLIVA/CIBERFES for Frailty and Healthy Aging, Blasco Ibañez, 15, 46010, Valencia, Spain. Electronic address: daniel.monleon@uv.es.
Enzo NisoliCenter of Study and Research on Obesity, Department of Medical Biotechnology and Translational Medicine, University of Milan, via Vanvitelli 32, 20129 Milan, Italy. Electronic address: enzo.nisoli@unimi.it.
Patrizia BrigidiHuman Microbiomics Unit, Department of Medical and Surgical Sciences, University of Bologna, via Massarenti 9, 40138 Bologna Italy. Electronic address: patrizia.brigidi@unibo.it.
Patricia IozzoInstitute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy. Electronic address: patricia.iozzo@cnr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe global prevalence of obesity and type 2 diabetes, particularly among children, is rising, yet the long-term impacts of early-life fecal microbiota transplantation (FMT) on metabolic health remain poorly understood.

objectivesTo investigate how early-life FMT from children to young, sex-matched mice influences metabolic outcomes and adipose tissue function in later, adult life.

methodsGerm-free mice were colonized with fecal microbiota from either lean children or children with obesity. The impacts on brown adipose tissue (BAT), white adipose tissue (WAT), glucose metabolism, and gut health were analyzed in male and female mice. Microbial communities and metabolite profiles were characterized using sequencing and metabolomics.

resultsMale mice receiving FMT from obese donors exhibited marked BAT whitening and impaired amino acid and glucose metabolism. In contrast, female recipients developed hyperglycemia, accompanied by gut barrier dysfunction and WAT impairment. Distinct microbial and metabolite profiles were associated with these phenotypes: Collinsella and trimethylamine in females; and Paraprevotella, Collinsella, Lachnospiraceae NK4A136, Bacteroides, Coprobacillus, and multiple metabolites in males. These phenotypic effects persisted despite changes in host environment and diet.

conclusionsEarly-life FMT induced long-lasting effects on the metabolic landscape, profoundly affecting adipose tissue function and systemic glucose homeostasis in adulthood. Donor dietary habits correlated with the fecal microbial profiles observed in recipient mice. These findings highlight the critical need for identifying and leveraging beneficial exposures during early development to combat obesity and diabetes.

Indexed as

Fecal Microbiota TransplantationGastrointestinal MicrobiomeIntestinesAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsChildFemaleGlucoseHumansMaleMiceMice, Inbred C57BLObesityGlucoseAdipose tissueGut microbiotaIntestinal permeabilityMetabolomicsObesityPositron emission tomographyType 2 diabetes

Identifiers

PMID40288637
PMCPMC12139018

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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.