Evidence map›Paper›PMID 37279927›Full record

ArticleJournal of Crohn's & colitis2023

Influence of Early Life Factors, including breast milk Composition, on the Microbiome of Infants Born to Mothers with and without Inflammatory Bowel Disease.

João Sabino, Leonid Tarassishin, Caroline Eisele, Kelly Hawkins, Amelie Barré, Nile Nair, Alexa Rendon, Anketse Debebe, Mellissa Picker, Manasi Agrawal and 12 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 6 institutions in 4 countries.

João SabinoIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Leonid TarassishinIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Caroline EiseleIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Kelly HawkinsIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Amelie BarréIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Nile NairIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Alexa RendonIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Anketse DebebeIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Mellissa PickerIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Manasi AgrawalIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Joanne StoneGastroenterology Division, Icahn School of Medicine at Mount Sinai, Department of Obstetrics, Gynecology and Reproductive Sciences, New York, NY, USA.
James GeorgeIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Peter LegnaniIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Elana MaserIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Ching-Lynn ChenGastroenterology Division, Icahn School of Medicine at Mount Sinai, Department of Obstetrics, Gynecology and Reproductive Sciences, New York, NY, USA.
Anne ThjømøeCALPRO AS, Lysaker, Norway.
Einar MørkCALPRO AS, Lysaker, Norway.
Marla DubinskyIcahn School of Medicine at Mount Sinai, Division of Pediatric Gastroenterology and Hepatology, New York, NY, USA.
Jianzhong HuIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Jean Frederic ColombelIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Inga PeterIcahn School of Medicine at Mount Sinai, Department of Genetics and Genomic Sciences, New York, NY, USA.
Joanna TorresIcahn School of Medicine at Mount Sinai, Division of Gastroenterology, Department of Medicine, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USCalpro (Norway) · NOAalborg University · DKHarvard University · USPennsylvania State University · USUniversity of Lisbon · PT

Funding

Effect of Maternal IBD, Microbiome and Early Life Events on the Bacterial Colonization and Mucosal Immunity in the OffspringR21DK125906 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CLEMENTE, JOSE C, PETER, INGA · 2021 to 2022
$465k
NIDDK NIH HHS R21 DK125906NIH HHS R21DK125906
6 · The paper itself

Abstract

BACKGROUND AND

aimsHerein we analysed the influence of early life factors, including breast milk composition, on the development of the intestinal microbiota of infants born to mothers with and without IBD.

methodsThe MECONIUM [Exploring MEChanisms Of disease traNsmission In Utero through the Microbiome] study is a prospective cohort study consisting of pregnant women with or without IBD and their infants. Longitudinal stool samples were collected from babies and analysed using 16s rRNA sequencing and faecal calprotectin. Breast milk proteomics was profiled using Olink inflammation panel.

resultsWe analysed gut microbiota of 1034 faecal samples from 294 infants [80 born to mothers with and 214 to mothers without IBD]. Alpha diversity was driven by maternal IBD status and time point. The major influencers of the overall composition of the microbiota were mode of delivery, feeding, and maternal IBD status. Specific taxa were associated with these exposures, and maternal IBD was associated with a reduction in Bifidobacterium. In 312 breast milk samples [91 from mothers with IBD], mothers with IBD displayed lower abundance of proteins involved in immune regulation, such as thymic stromal lymphopoietin, interleukin-12 subunit beta, tumour necrosis factor-beta, and C-C motif chemokine 20, as compared with control mothers [adjusted p = 0.0016, 0.049, 0.049, and 0.049, respectively], with negative correlations with baby´s calprotectin, and microbiome at different time points.

conclusionMaternal IBD diagnosis influences microbiota in their offspring during early life. The proteomic profile of breast milk of women with IBD differs from that of women without IBD, with distinct time-dependent associations with baby's gut microbiome and feacal calprotectin.

Indexed as

Inflammatory Bowel DiseasesMicrobiotaFecesFemaleHumansInfantLeukocyte L1 Antigen ComplexMilk, HumanMothersPregnancyProspective StudiesProteomicsRNA, Ribosomal, 16SLeukocyte L1 Antigen ComplexRNA, Ribosomal, 16Sbreast milkEarly lifeIBDmicrobiota

Identifiers

PMID37279927
PMCPMC10673817
OpenAlexW4379600785

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.