Evidence map›Paper›PMID 33144591›Full record

ArticleScientific reports2020

Exclusive enteral nutrition mediates gut microbial and metabolic changes that are associated with remission in children with Crohn's disease.

Kay Diederen, Jia V Li, Gillian E Donachie, Tim G de Meij, Dirk R de Waart, Theodorus B M Hakvoort, Angelika Kindermann, Josef Wagner, Victoria Auyeung, Anje A Te Velde and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 3 pooled it
5.7field-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

80 citing papers in PubMed, 3 syntheses or guidelines pooled it, 106 citations in OpenAlex.

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20 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

16 authors at 5 institutions in 2 countries.

Kay DiederenDepartment of Pediatric Gastroenterology and Nutrition, Amsterdam UMC, Location AMC & VUmc, Amsterdam, The Netherlands.
Jia V LiDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Gillian E DonachieThe Rowett Institute, University of Aberdeen, Aberdeen, UK.
Tim G de MeijDepartment of Pediatric Gastroenterology and Nutrition, Amsterdam UMC, Location AMC & VUmc, Amsterdam, The Netherlands.
Dirk R de WaartTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands.
Theodorus B M HakvoortTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands.
Angelika KindermannDepartment of Pediatric Gastroenterology and Nutrition, Amsterdam UMC, Location AMC & VUmc, Amsterdam, The Netherlands.
Josef WagnerPathogen Genomics Group, Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.
Victoria AuyeungDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Anje A Te VeldeTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands.
Sigrid E M HeinsbroekTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands.
Marc A BenningaDepartment of Pediatric Gastroenterology and Nutrition, Amsterdam UMC, Location AMC & VUmc, Amsterdam, The Netherlands.
James KinrossDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Alan W WalkerThe Rowett Institute, University of Aberdeen, Aberdeen, UK.
Wouter J de JongeTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands.
Jurgen SeppenTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Meibergdreef 69, 1105BK, Amsterdam, The Netherlands. j.seppen@amsterdamumc.nl.
Amsterdam University Medical Centers · NLAsser Institute · NLImperial College London · GBUniversity of Aberdeen · GBWellcome Sanger Institute · GB

Funding

Randomized Controlled Trial of Resistant Starch to Reduce Colon Cancer Risk in Alaska Native PeopleR01CA204403 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI O'KEEFE, STEPHEN J.D., THOMAS, TIMOTHY K · 2017 to 2021
$2.8M
Department of Health II-OL-1116-10027Medical Research Council MR/P002536/1NCI NIH HHS R01 CA204403Wellcome TrustWellcome Trust 098051
6 · The paper itself

Abstract

A nutritional intervention, exclusive enteral nutrition (EEN) can induce remission in patients with pediatric Crohn's disease (CD). We characterized changes in the fecal microbiota and metabolome to identify the mechanism of EEN. Feces of 43 children were collected prior, during and after EEN. Microbiota and metabolites were analyzed by 16S rRNA gene amplicon sequencing and NMR. Selected metabolites were evaluated in relevant model systems. Microbiota and metabolome of patients with CD and controls were different at all time points. Amino acids, primary bile salts, trimethylamine and cadaverine were elevated in patients with CD. Microbiota and metabolome differed between responders and non-responders prior to EEN. EEN decreased microbiota diversity and reduced amino acids, trimethylamine and cadaverine towards control levels. Patients with CD had reduced microbial metabolism of bile acids that partially normalized during EEN. Trimethylamine and cadaverine inhibited intestinal cell growth. TMA and cadaverine inhibited LPS-stimulated TNF-alpha and IL-6 secretion by primary human monocytes. A diet rich in free amino acids worsened inflammation in the DSS model of intestinal inflammation. Trimethylamine, cadaverine, bile salts and amino acids could play a role in the mechanism by which EEN induces remission. Prior to EEN, microbiota and metabolome are different between responders and non-responders.

Indexed as

AdolescentAmino AcidsBacteriaBiodiversityCadaverineCase-Control StudiesChildCrohn DiseaseEnteral NutritionFecesFemaleGastrointestinal MicrobiomeHigh-Throughput Nucleotide SequencingHumansInterleukin-6LipopolysaccharidesAmino AcidsCadaverineIL6 protein, humanInterleukin-6LipopolysaccharidesMethylaminesRNA, Ribosomal, 16Strimethylamine

Identifiers

PMID33144591
PMCPMC7609694
OpenAlexW3096326741

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.