Evidence map›Paper›PMID 40140438›Full record

ArticleScientific reports2025

Longitudinal fecal microbiota and volatile metabolomics preceding necrotizing enterocolitis in preterm infants: a case-control study.

S El Manouni El Hassani, N M Frerichs, D J C Berkhout, T Nijsen, H H Knobel, H Weda, M Xu, X Long, L Wijnoltz, M M van Weissenbruch and 13 more

Erratum issuedAbstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

S El Manouni El HassaniDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
N M FrerichsDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands. n.m.frerichs@amsterdamumc.nl.
D J C BerkhoutDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
T NijsenPhilips S&RC Research & Development, Eindhoven, The Netherlands.
H H KnobelEurofins EAG, Eurofins Materials Science Netherlands B.V., Eindhoven, The Netherlands.
H WedaNetherlands Institute for Public Safety, Arnhem, The Netherlands.
M XuLighting and IoT Lab, Department of Electrical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
X LongBiomedical Diagnostics Lab, Department of Electrical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
L WijnoltzPhilips Research, Eindhoven, The Netherlands.
M M van WeissenbruchAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, The Netherlands.
A H van KaamAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, The Netherlands.
V CosseyNeonatal Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
C F W PeetersMathematical and Statistical Methods Group (Biometris), Wageningen University & Research, Wageningen, The Netherlands.
R A van LingenNeonatal Intensive Care Unit, Amalia Children's Centre, Isala, Zwolle, The Netherlands.
C V HulzebosNeonatal Intensive Care Unit, Beatrix Children's Hospital/University Medical Centre Groningen, Groningen, The Netherlands.
D C VijlbriefNeonatal Intensive Care Unit, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands.
W P de BoodeNeonatal Intensive Care Unit, Radboud University Medical Centre, Radboud Institute for Health Sciences, Amalia Children's Hospital, Nijmegen, The Netherlands.
B W KramerDepartment of Pediatrics, Maastricht University Medical Center, Maastricht, The Netherlands.
A E BuddinginBiome BV, Amsterdam, The Netherlands.
M A BenningaDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
N K H de BoerDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
H J NiemarktNeonatal Intensive Care Unit, Máxima Medical Center, Veldhoven, The Netherlands.
T G J de MeijDepartment of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alterations in fecal microbiota and volatile organic compound (VOC) profiles of preterm infants have been demonstrated before onset of necrotizing enterocolitis (NEC). However, NEC-specific signatures need to be identified before potential application as predictive biomarker in clinical practice. A prospective multicenter case-control study was conducted to identify preclinical fecal microbiota and VOC profiles of infants that developed NEC. Microbiota analysis (PCR-based IS-pro technique) and VOC analysis (gas chromatography-mass spectrometry) were performed on fecal samples collected up to three days before clinical NEC onset. In 112 infants (56 NEC, 56 matched controls), sufficient number fecal samples were collected for either microbiota or VOC analysis. Prior to NEC onset, Clostridium perfringens (p = 0.023, unadjusted) was more present in infants with NEC, versus controls. VOC analysis showed a clear distinction between fecal profiles of NEC cases and controls (area under the curve = 0.82). Fourteen unique VOC features contributed to this discrimination. Fecal microbiota and VOC profiles may serve as early indicators of NEC, and allow for increased understanding of pathophysiological mechanisms of NEC, but larger validation cohorts are needed before an overarching NEC-specific predictive microbiota-based biomarker can be implemented.

Indexed as

Enterocolitis, NecrotizingFecesGastrointestinal MicrobiomeMetabolomicsVolatile Organic CompoundsBiomarkersCase-Control StudiesClostridium perfringensFemaleHumansInfant, NewbornInfant, PrematureMaleProspective StudiesBiomarkersVolatile Organic CompoundsMetabolomicsMicrobiomeNecrotizing enterocolitisStoolVolatile organic compounds

Identifiers

PMID40140438
PMCPMC11947453

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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.