Evidence map›Paper›PMID 41047527›Full record

ArticleJPEN. Journal of parenteral and enteral nutrition2026

The relationship between infant feeding types, gut microbiome, intestinal inflammation, and neurodevelopment in a neonatal piglet model.

Heidi Sellmann, Janet E Williams, Klas Udekwu, Ashley McDonough, Katie Heckathorn, Laurel Nuñez, Yimin Chen

Abstract read
In one paragraph

Article in JPEN. Journal of parenteral and enteral nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Heidi SellmannUniversity of Idaho, Moscow, Idaho, USA.ORCID https://orcid.org/0009-0001-8515-8573
Janet E WilliamsUniversity of Idaho, Moscow, Idaho, USA.ORCID https://orcid.org/0000-0002-9769-1789
Klas UdekwuUniversity of Idaho, Moscow, Idaho, USA.
Ashley McDonoughUniversity of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-3864-9449
Katie HeckathornUniversity of Idaho, Moscow, Idaho, USA.
Laurel NuñezUniversity of Idaho, Moscow, Idaho, USA.ORCID https://orcid.org/0000-0001-7741-1527
Yimin ChenUniversity of Idaho, Moscow, Idaho, USA.ORCID https://orcid.org/0000-0003-2246-7587

Funding

NCCIH Supplement to NCATS/CTSA Program for KL2 Scholars - M. SoddersKL2TR002317 · NCATS · UNIVERSITY OF WASHINGTON · PI Christy Michelle McKinney · 2017 to 2026
$14.5M
Research Project - RPL LaneP20GM152304 · NIGMS · UNIVERSITY OF IDAHO · PI MICHELLE Kay MCGUIRE · 2024 to 2026
$8.9M
NCATS NIH HHS KL2 TR002317NIGMS NIH HHS P20 GM152304The project described was supported by an American Society for Parenteral and Enteral Nutrition Rhoads Research Foundation Research Grant. This publication was made possible by an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health (NIH), the NIH Office of Women's Health and the NIH Office of Nutrition Research under grant #P20GM152304. Additional funding was provided by the National Center for Advancing Translational Sciences of the NIH under award No. KL2TR002317
6 · The paper itself

Abstract

backgroundThe influences of nutrition on the infant's developing gastrointestinal (GI) microbiome, intestinal tract, and brain is unclear. Human milk (HM) is associated with beneficial immune and cognitive development compared with infant formula (IF). This study used a neonatal piglet model to determine the effects of infant feeding exposures (HM vs IF) on the GI microbiome, intestinal inflammation, and brain oligodendrocyte maturation.

methodsSix pairs of piglets received HM or IF for 28 days. Fecal samples were collected weekly and GI regions (jejunum, ileum, and colon) and brains were harvested at necropsy. Fecal microbiome composition was determined by 16S ribosomal RNA (16S rRNA) sequencing. Intestinal inflammation was assessed via quantification of intestinal interleukin (IL)-1β, IL-8, IL-10, tumor necrosis factor (TNF)-α, and fecal calprotectin. Neurodevelopment was evaluated by quantifying mature and immature oligodendrocytes in gray and white matter.

resultsBacterial community composition differed between feeding groups (P < 0.002) and over time (P = 0.001). Various highly abundant genera were associated with changes over time (P < 0.05) and only Escherichia-Shigella was associated with feeding group by time interactions (P < 0.05). No differences were found in intestinal inflammatory markers between feeding types, but mature oligodendrocytes in white matter were higher in HM-fed piglets (P = 0.004). Various intestinal inflammatory markers and relatively highly abundant genera were significantly associated.

conclusionPiglet fecal bacterial compositions differed by feeding group and over time, with several relatively highly abundant genera associated with intestinal inflammatory markers. Additionally, HM may support proper white matter development. Future research should investigate mechanisms underlying these relationships.

Indexed as

Gastrointestinal MicrobiomeInfant FormulaInflammationIntestinesMilk, HumanAnimalsAnimals, NewbornBrainFecesFemaleHumansOligodendrogliaRNA, Ribosomal, 16SSwineRNA, Ribosomal, 16Sinfant nutritionintestinal inflammationmicrobiomeneurodevelopmentpiglet model

Identifiers

PMID41047527
PMCPMC12775721

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LicenceCC BY-NC-ND
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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.