Evidence map›Paper›PMID 32693091›Full record

Trial reportThe Journal of allergy and clinical immunology2020

Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age.

Andréanne Morin, Chris G McKennan, Casper-Emil T Pedersen, Jakob Stokholm, Bo L Chawes, Ann-Marie Malby Schoos, Katherine A Naughton, Jonathan Thorsen, Martin S Mortensen, Donata Vercelli and 6 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
13.9field-weighted citation impact, top 1% of its field
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

42 citing papers in PubMed, 71 citations in OpenAlex.

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  19. La Tunisie medicale · 2024
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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

16 authors at 5 institutions in 2 countries.

Andréanne MorinDepartments of Human Genetics, The University of Chicago, Chicago, Ill.
Chris G McKennanDepartments of Statistics, The University of Chicago, Chicago, Ill.
Casper-Emil T PedersenCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Jakob StokholmCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Bo L ChawesCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Ann-Marie Malby SchoosCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Katherine A NaughtonDepartments of Human Genetics, The University of Chicago, Chicago, Ill.
Jonathan ThorsenCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Martin S MortensenSection of Microbiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Donata VercelliDepartment of Cellular and Molecular Medicine, University of Arizona Health Sciences, Tucson, Ariz; Asthma and Airway Disease Research Center, University of Arizona Health Sciences, Tucson, Ariz.
Urvish TrivediSection of Microbiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Søren J SørensenSection of Microbiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Hans BisgaardCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Dan L NicolaeDepartments of Human Genetics, The University of Chicago, Chicago, Ill; Departments of Statistics, The University of Chicago, Chicago, Ill.
Klaus BønnelykkeCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, Copenhagen, Denmark.
Carole OberDepartments of Human Genetics, The University of Chicago, Chicago, Ill. Electronic address: c-ober@genetics.uchicago.edu.
University of Chicago · USCopenhagen Prospective Studies on Asthma in Childhood · DKGentofte Hospital · DKUniversity of Copenhagen · DKUniversity of Arizona · US

Funding

Prenatal Origins of AsthmaR01HL129735 · NHLBI · UNIVERSITY OF CHICAGO · PI BISGAARD, HANS, OBER, CAROLE · 2015 to 2018
$3.2M
Role of Gamma delta-17 T Cells in Asthma Protection by Amish Farm Exposure .R21AI144722 · NIAID · UNIVERSITY OF ARIZONA · PI VERCELLI, DONATA · 2019 to 2020
$443k
Interactions between Environmental Microbiome, Maternal Immunity, Neonatal Epigenome and Respiratory Microbiome Development as Determinants of Asthma In ChildhoodR21AI133765 · NIAID · UNIVERSITY OF ARIZONA · PI LYNCH, SUSAN VERONICA, VERCELLI, DONATA · 2017 to 2018
$439k
NHLBI NIH HHS R01 HL129735NIAID NIH HHS R21 AI133765NIAID NIH HHS R21 AI144722
6 · The paper itself

Abstract

backgroundThe upper airways present a barrier to inhaled allergens and microbes, which alter immune responses and subsequent risk for diseases, such as allergic rhinitis (AR).

objectiveWe tested the hypothesis that early-life microbial exposures leave a lasting signature in DNA methylation that ultimately influences the development of AR in children.

methodsWe studied upper airway microbiota at 1 week, 1 month, and 3 months of life, and measured DNA methylation and gene expression profiles in upper airway mucosal cells and assessed AR at age 6 years in children in the Copenhagen Prospective Studies on Asthma in Childhood birth cohort.

resultsWe identified 956 AR-associated differentially methylated CpGs in upper airway mucosal cells at age 6 years, 792 of which formed 3 modules of correlated differentially methylated CpGs. The eigenvector of 1 module was correlated with the expression of genes enriched for lysosome and bacterial invasion of epithelial cell pathways. Early-life microbial diversity was lower at 1 week (richness P = .0079) in children with AR at age 6 years, and reduced diversity at 1 week was also correlated with the same module's eigenvector (ρ = -0.25; P = 3.3 × 10

conclusionsOur results suggest that upper airway microbial composition in infancy contributes to the development of AR during childhood, and this trajectory is mediated, at least in part, through altered DNA methylation patterns in upper airway mucosal cells.

Indexed as

DNA MethylationEpigenesis, GeneticMicrobiotaRhinitis, AllergicChildFemaleHumansInfantInfant, NewbornMaleNoseProspective StudiesAllergic rhinitisDNA methylationearly lifegene expressionmicrobiotaupper airways

Identifiers

PMID32693091
PMCPMC7821422
OpenAlexW3042311706

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.