Evidence map›Paper›PMID 29921329›Full record

ArticleMicrobiome2018

Metabolomic signatures distinguish the impact of formula carbohydrates on disease outcome in a preterm piglet model of NEC.

Lee Call, Barbara Stoll, Berthe Oosterloo, Nadim Ajami, Fariha Sheikh, Anja Wittke, Rosaline Waworuntu, Brian Berg, Joseph Petrosino, Oluyinka Olutoye and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbiome, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
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  9. Term infant formula macronutrient composition: An update for clinicians.Journal of pediatric gastroenterology and nutrition · 2025
    Review
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  11. Article
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  17. Frontiers in microbiology · 2022
    Article
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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

11 authors at 3 institutions in 1 country.

Lee CallDepartment Pediatric Gastroenterology, Hepatology, and Nutrition, USDA-ARS Children's Nutrition Research Center, 1100 Bates Ave, Houston, TX, 77030, USA.
Barbara StollDepartment Pediatric Gastroenterology, Hepatology, and Nutrition, USDA-ARS Children's Nutrition Research Center, 1100 Bates Ave, Houston, TX, 77030, USA.
Berthe OosterlooDepartment Pediatric Gastroenterology, Hepatology, and Nutrition, USDA-ARS Children's Nutrition Research Center, 1100 Bates Ave, Houston, TX, 77030, USA.
Nadim AjamiAlkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, One Baylor Plaza, MS BCM385, Houston, TX, 77030, USA.
Fariha SheikhDivision of Pediatric Surgery, Baylor College of Medicine, 6701 Fannin St, Suite 1210, Houston, TX, 77030, USA.
Anja WittkeMead Johnson Pediatric Nutrition Institute, 2400 W Lloyd Expressway, Evansville, IN, 47712, USA.
Rosaline WaworuntuMead Johnson Pediatric Nutrition Institute, 2400 W Lloyd Expressway, Evansville, IN, 47712, USA.
Brian BergMead Johnson Pediatric Nutrition Institute, 2400 W Lloyd Expressway, Evansville, IN, 47712, USA.
Joseph PetrosinoAlkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, One Baylor Plaza, MS BCM385, Houston, TX, 77030, USA.
Oluyinka OlutoyeDivision of Pediatric Surgery, Baylor College of Medicine, 6701 Fannin St, Suite 1210, Houston, TX, 77030, USA.
Douglas BurrinDepartment Pediatric Gastroenterology, Hepatology, and Nutrition, USDA-ARS Children's Nutrition Research Center, 1100 Bates Ave, Houston, TX, 77030, USA. doug.burrin@ars.usda.gov.ORCID 0000-0002-8792-3339
Baylor College of Medicine · USChildren's Nutrition Research Center at Baylor College of Medicine · USMead Johnson (United States) · US

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Geoffrey A Preidis · 2001 to 2026
$28.3M
TRAINING PROGRAM IN COMPUTATIONAL BIOLOGY AND MEDICINET15LM007093 · NLM · RICE UNIVERSITY · PI Lydia E. Kavraki · 1992 to 2026
$20.8M
Training Program in Translational Biology and Molecular MedicineT32GM088129 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI ROONEY, CLIONA M., VAN DEN VEYVER, IGNATIA B · 2010 to 2019
$3.0M
NIDDK NIH HHS P30 DK056338NIGMS NIH HHS T32 GM088129NLM NIH HHS T15 LM007093
6 · The paper itself

Abstract

backgroundMajor risk factors for necrotizing enterocolitis (NEC) include premature birth and formula feeding in the context of microbial colonization of the gastrointestinal tract. We previously showed that feeding formula composed of lactose vs. corn syrup solids protects against NEC in preterm pigs; however, the microbial and metabolic effects of these different carbohydrates used in infant formula has not been explored.

objectiveOur objective was to characterize the effects of lactose- and corn syrup solid-based formulas on the metabolic and microbial profiles of preterm piglets and to determine whether unique metabolomic or microbiome signatures correlate with severity or incidence of NEC. DESIGN/

methodsPreterm piglets (103 days gestation) were given total parenteral nutrition (2 days) followed by gradual (5 days) advancement of enteral feeding of formulas matched in nutrient content but containing either lactose (LAC), corn syrup solids (CSS), or 1:1 mix (MIX). Gut contents and mucosal samples were collected and analyzed for microbial profiles by sequencing the V4 region of the 16S rRNA gene. Metabolomic profiles of cecal contents and plasma were analyzed by LC/GC mass spectrometry.

resultsNEC incidence was 14, 50, and 44% in the LAC, MIX, and CSS groups, respectively. The dominant classes of bacteria were Bacilli, Clostridia, and Gammaproteobacteria. The number of observed OTUs was lowest in colon contents of CSS-fed pigs. CSS-based formula was associated with higher Bacilli and lower Clostridium from clusters XIVa and XI in the colon. NEC was associated with decreased Gammaproteobacteria in the stomach and increased Clostridium sensu stricto in the ileum. Plasma from NEC piglets was enriched with metabolites of purine metabolism, aromatic amino acid metabolism, and bile acids. Markers of glycolysis, e.g., lactate, were increased in the cecal contents of CSS-fed pigs and in plasma of pigs which developed NEC.

conclusionsFeeding formula containing lactose is not completely protective against NEC, yet selects for greater microbial richness associated with changes in Bacilli and Clostridium and lower NEC incidence. We conclude that feeding preterm piglets a corn syrup solid vs. lactose-based formula increases the incidence of NEC and produces distinct metabolomic signatures despite modest changes in microbiome profiles.

Indexed as

Dietary CarbohydratesEnteral NutritionAnimal FeedAnimalsBacillusClostridiumEnterocolitis, NecrotizingFemaleGammaproteobacteriaGastrointestinal MicrobiomeGastrointestinal TractHigh Fructose Corn SyrupLactosePregnancyPremature BirthRisk FactorsDietary CarbohydratesHigh Fructose Corn SyrupLactoseRNA, Ribosomal, 16SClostridiumCorn syrup solidsInfant formulaLactateLactoseMaltodextrinNecrotizing enterocolitis

Identifiers

PMID29921329
PMCPMC6009052
OpenAlexW2809235064

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.