Evidence map›Paper›PMID 40238773›Full record

ArticlePloS one2025

EGF and IgA in maternal milk, donor milk, and milk fortifiers in the neonatal intensive care unit setting.

Christian Tamar, Kara Greenfield, Katya McDonald, Emily Levy, Jane E Brumbaugh, Kathryn Knoop

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Christian TamarDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0009-0002-4191-5533
Kara GreenfieldDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0000-0002-1315-5146
Katya McDonaldDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0000-0001-8919-3651
Emily LevyDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
Jane E BrumbaughDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0000-0003-1078-3320
Kathryn KnoopDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, United States of America.ORCID 0000-0003-2007-3066

Funding

Immune Outcomes to Neonatal Antigen Delivery in the IntestineR01DK134366 · NIDDK · MAYO CLINIC ROCHESTER · PI Kathryn A Knoop · 2023 to 2026
$1.5M
NIDDK NIH HHS R01 DK134366
6 · The paper itself

Abstract

Human milk contains a variety of factors that positively contribute to neonatal health, including epidermal growth factor (EGF) and immunoglobulin A (IgA). When maternal milk cannot be the primary diet, maternal milk alternatives like donor human milk or formula can be provided. Donor human milk is increasingly provided to infants born preterm or low birth weight with the aim to supply immunological factors at similar concentrations to maternal milk. We sought to assess the concentrations of human EGF and IgA in the diet and stool of neonates between exclusive maternal milk, donor human milk, or formula-based diets. Using a prospective cohort study, we collected samples of diet and stool weekly from premature and low birth weight neonates starting at 10 days postnatal through five weeks of life while admitted to a neonatal intensive care unit (NICU). Compared to formula, there was significantly more EGF in both the milk and the stool of the infants fed human milk. Donor milk pooled from multiple donors contained similar concentrations of EGF and IgA to maternal milk, which was also significantly more than formula diets. Maternal milk supplemented with a fortifier derived from human milk contained significantly more EGF and IgA compared to unfortified maternal milk or maternal milk supplemented with fortifier derived from bovine milk. Further analysis of human milk-derived fortifiers confirmed these fortifiers contained significant concentrations of EGF and IgA, contributing to an increased concentration of those factors that bovine milk-derived fortifiers do not confer. These findings illustrate how the choice of diet for a newborn, and even how that diet is modified through fortifiers or pasteurization before ingestion, impacts the beneficial biomolecules the infant receives from feeding.

Indexed as

Epidermal Growth FactorFood, FortifiedImmunoglobulin AIntensive Care Units, NeonatalMilk, HumanFecesFemaleHumansInfant FormulaInfant, NewbornInfant, PrematureMaleProspective StudiesEpidermal Growth FactorImmunoglobulin A

Identifiers

PMID40238773
PMCPMC12002475

What OpenQuestion holds

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LicenceCC BY
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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.