Evidence map›Paper›PMID 35853977›Full record

ArticleScientific reports2022

Fecal amine metabolite analysis before onset of severe necrotizing enterocolitis in preterm infants: a prospective case-control study.

N Deianova, S El Manouni El Hassani, E A Struijs, E E W Jansen, A Bakkali, M A van de Wiel, W P de Boode, C V Hulzebos, A H van Kaam, B W Kramer and 8 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

18 authors at 10 institutions in 1 country.

N DeianovaDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands. n.deianova@amsterdamumc.nl.
S El Manouni El HassaniDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands.
E A StruijsDepartment of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
E E W JansenDepartment of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
A BakkaliDepartment of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
M A van de WielDepartment of Epidemiology and Data Science, Amsterdam Public Health Research Institute, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
W P de BoodeDepartment of Neonatology, Amalia Children's Hospital, Radboud UMC, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.
C V HulzebosDivision of Neonatology, University Medical Center Groningen, Beatrix Children's Hospital, University of Groningen, Groningen, The Netherlands.
A H van KaamDepartment of Neonatology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
B W KramerNeonatal Intensive Care Unit, Department of Pediatrics, Maastricht UMC, Maastricht, The Netherlands.
E d'HaensNeonatal Intensive Care Unit, Amalia Children's Center, Isala, Zwolle, The Netherlands.
D C VijlbriefNeonatal Intensive Care Unit, UMC Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
M M van WeissenbruchDepartment of Neonatology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
W J de JongeAmsterdam Gastroenterology Endocrinology Metabolism (AGEM) Research Institute, Amsterdam UMC, University of Amsterdam, Tytgat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands.
M A BenningaDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, Amsterdam, The Netherlands.
H J NiemarktDepartment of Neonatology, Máxima Medical Center, Veldhoven, The Netherlands.
N K H de BoerDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism (AGEM) Research Institute, Amsterdam, The Netherlands.
T G J de MeijDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands.
Amsterdam University Medical Centers · NLEmma Kinderziekenhuis · NLUniversity of Amsterdam · NLVrije Universiteit Amsterdam · NLIsala · NLMaastricht University Medical Centre · NLRadboud University Medical Center · NLRadboud University Nijmegen · NLUniversity of Groningen · NLWilhelmina Children's Hospital · NL

Funding

Marie Curie No 814168
6 · The paper itself

Abstract

Infants developing necrotizing enterocolitis (NEC) have a different metabolomic profile compared to controls. The potential of specific metabolomics, i.e. amino acids and amino alcohols (AAA), as early diagnostic biomarkers for NEC is largely unexplored. In this multicenter prospective case-control study, longitudinally collected fecal samples from preterm infants (born <30 weeks of gestation) from 1-3 days before diagnosis of severe NEC (Bell's stage IIIA/IIIB), were analyzed by targeted high-performance liquid chromatography (HPLC). Control samples were collected from gestational and postnatal age-matched infants. Thirty-one NEC cases (15 NEC IIIA;16 NEC IIIB) with 1:1 matched controls were included. Preclinical samples of infants with NEC were characterized by five increased essential amino acids-isoleucine, leucine, methionine, phenylalanine and valine. Lysine and ethanolamine ratios were lower prior to NEC, compared to control samples. A multivariate model was rendered based on isoleucine, lysine, ethanolamine, tryptophan and ornithine, modestly discriminating cases from controls (AUC 0.67; p < 0.001). Targeted HPLC pointed to several specific AAA alterations in samples collected 1-3 days before NEC onset, compared to controls. Whether this reflects metabolic alterations and has a role in early biomarker development for NEC, has yet to be elucidated.

Indexed as

Enterocolitis, NecrotizingInfant, Newborn, DiseasesAminesCase-Control StudiesEthanolaminesHumansInfantInfant, NewbornInfant, PrematureIsoleucineLysineAminesEthanolaminesIsoleucineLysine

Identifiers

PMID35853977
PMCPMC9296556
OpenAlexW4285798917

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.