Evidence map›Paper›PMID 26251473›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2015

Glycomacropeptide is a prebiotic that reduces Desulfovibrio bacteria, increases cecal short-chain fatty acids, and is anti-inflammatory in mice.

Emily A Sawin, Travis J De Wolfe, Busra Aktas, Bridget M Stroup, Sangita G Murali, James L Steele, Denise M Ney

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

92 citing papers in PubMed, 2 syntheses or guidelines pooled it, 181 citations in OpenAlex.

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  18. Human milkFrontiers in nutrition · 2025
    Review
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32 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Emily A SawinDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and.
Travis J De WolfeDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin.
Busra AktasDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin.
Bridget M StroupDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and.
Sangita G MuraliDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and.
James L SteeleDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin.
Denise M NeyDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin; and ney@nutrisci.wisc.edu.
University of Wisconsin–Madison · US

Funding

TRAINING IN NUTRITIONT32DK007665 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GUY E GROBLEWSKI, Chi- Liang Eric Yen · 1993 to 2026
$9.2M
NIDDK NIH HHS T32 DK 007665NIDDK NIH HHS T32 DK007665
6 · The paper itself

Abstract

Glycomacropeptide (GMP) is a 64-amino acid (AA) glycophosphopeptide with application to the nutritional management of phenylketonuria (PKU), obesity, and inflammatory bowel disease (IBD). GMP is a putative prebiotic based on extensive glycosylation with sialic acid, galactose, and galactosamine. Our objective was to determine the prebiotic properties of GMP by characterizing cecal and fecal microbiota populations, short-chain fatty acids (SCFA), and immune responses. Weanling PKU (Pah(enu2)) and wild-type (WT) C57Bl/6 mice were fed isoenergetic AA, GMP, or casein diets for 8 wk. The cecal content and feces were collected for microbial DNA extraction to perform 16S microbiota analysis by Ion Torrent PGM sequencing. SCFA were determined by gas chromatography, plasma cytokines via a Bio-Plex Pro assay, and splenocyte T cell populations by flow cytometry. Changes in cecal and fecal microbiota are primarily diet dependent. The GMP diet resulted in a reduction from 30-35 to 7% in Proteobacteria, genera Desulfovibrio, in both WT and PKU mice with genotype-dependent changes in Bacteroidetes or Firmicutes. Cecal concentrations of the SCFA acetate, propionate, and butyrate were increased with GMP. The percentage of stimulated spleen cells producing interferon-γ (IFN-γ) was significantly reduced in mice fed GMP compared with casein. In summary, plasma concentrations of IFN-γ, TNF-α, IL-1β, and IL-2 were reduced in mice fed GMP. GMP is a prebiotic based on reduction in Desulfovibrio, increased SCFA, and lower indexes of inflammation compared with casein and AA diets in mice. Functional foods made with GMP may be beneficial in the management of PKU, obesity, and IBD.

Indexed as

AnimalsCaseinsCecumCytokinesDesulfovibrioFatty Acids, VolatileFecesFemaleFlow CytometryGastrointestinal MicrobiomeMaleMiceMice, Inbred C57BLPeptide FragmentsPhenylketonuriasPrebioticscaseinomacropeptideCaseinsCytokinesFatty Acids, VolatilePeptide FragmentsPrebioticscytokinesinflammatory bowel diseasephenylketonuriasialic acidsulfate reducing bacteria

Identifiers

PMID26251473
PMCPMC4593820
OpenAlexW2321624725

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.