Evidence map›Paper›PMID 39932047›Full record

ArticlePediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology2025

The Janus face of Bifidobacterium in the development of atopic eczema: A role for compositional maturation.

Martin Depner, Diana Hazard Taft, Stefanie Peschel, Caroline Roduit, Anne M Karvonen, Cindy Barnig, Amandine Divaret-Chauveau, Josef Riedler, Juha Pekkanen, Elisabeth Schmausser-Hechfellner and 10 more

Abstract read
In one paragraph

Article in Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. The Janus face of Bifidobacterium in the development of atopic eczema: A role for compositional maturation.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    Article
  5. 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

20 authors.

Martin DepnerInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Diana Hazard TaftFood Science and Technology, University of California, Davis, California, USA.
Stefanie PeschelInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Caroline RoduitChristine Kühne Center for Allergy Research and Education (CK-CARE), Davos, Switzerland.
Anne M KarvonenDepartment of Health Security, National Institute for Health and Welfare, Kuopio, Finland.
Cindy BarnigDepartment of Respiratory Disease, University Hospital of Besançon, Besançon, France.
Amandine Divaret-ChauveauPediatric Allergy Department, Children's Hospital, University Hospital of Nancy, Vandoeuvre les Nancy, France.ORCID https://orcid.org/0000-0002-2492-9864
Josef RiedlerChildren's Hospital Schwarzach, Schwarzach, Austria.
Juha PekkanenDepartment of Health Security, National Institute for Health and Welfare, Kuopio, Finland.
Elisabeth Schmausser-HechfellnerInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Giulia PaganiInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Roger LauenerChristine Kühne Center for Allergy Research and Education (CK-CARE), Davos, Switzerland.
Marjut RoponenDepartment of Environmental and Biological Sciences, University of Eastern Finland, Kuopio, Finland.
Harald RenzInstitute for Medicine Laboratory, Pathobiochemistry and Molecular Diagnostics, Philipps-University Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0003-0602-7215
Petra Ina PfefferleGerman Center for Lung Research (DZL), Sites Marburg and Munich, Germany.
Bianca SchaubGerman Center for Lung Research (DZL), Sites Marburg and Munich, Germany.ORCID https://orcid.org/0000-0003-1652-8873
Erika von MutiusInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Pirkka V KirjavainenDepartment of Health Security, National Institute for Health and Welfare, Kuopio, Finland.
Markus J EgeInstitute of Asthma and Allergy Prevention, Helmholtz Zentrum Munich, German Research Center for Environmental Health, Neuherberg, Germany.ORCID https://orcid.org/0000-0001-6643-3923
PASTURE study group

Funding

Academy of FinlandDeutsches Zentrum für LungenforschungEmil Aaltosen SäätiöEuropean CommissionEuropean Research CouncilJuho Vainion SäätiöPäivikki ja Sakari Sohlbergin SäätiöYrjö Jahnssonin Säätiö
6 · The paper itself

Abstract

backgroundAtopic eczema often develops in the first year of life, when the composition of the gut microbiota is most plastic as illustrated by the decrease in bifidobacteria after weaning. This may provide the opportunity for microbial stimuli and their environmental determinants to alter the disease course.

objectivesTo determine the role of the genus Bifidobacterium for atopic eczema in early childhood.

methodsWe analysed the bacterial composition in fecal samples of 618 children of the PASTURE ("Protection against Allergy-Study in Rural Environments") birth cohort using 16S rRNA amplicon sequencing of fecal samples collected at 2 and 12 months of age. Atopic eczema was defined as a parent-reported doctor's diagnosis until 2 years, and patterns of rash symptoms were classified by latent class analysis. We applied mediation models to assess direct and microbiota-mediated effects of environmental determinants on atopic eczema.

resultsThe Bifidobacterium composition observed at 2 months was inversely related to atopic eczema (OR = 0.68 [0.53-0.87], p = .002) and persistent rash. This association was not seen at 12 months, when the composition of Bifidobacterium amplicon sequence variants (ASVs) was altered. The effect of beneficial ASVs at 2 months (OR = 0.72 [0.57-0.91]) was lost at 12 months (OR = 0.97 [0.76-1.24]), when distinct bifidobacteria tended to be positively related to late-onset rash.

conclusionsThe subgenus composition of Bifidobacterium undergoes substantial changes in the first year of life. The protective effect of Bifidobacterium depends on the ASV composition at the respective age of the infant, highlighting the importance of timing in prevention strategies targeting infant-microbe interactions.

Indexed as

BifidobacteriumDermatitis, AtopicGastrointestinal MicrobiomeFecesFemaleHumansInfantMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16Satopic eczemaBifidobacteriumcompositional maturationlate‐onset rashpersistent rashsubgenus compositiontransient rashwindow of opportunity

Identifiers

PMID39932047
PMCPMC11812080

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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.