Evidence map›Paper›PMID 29053703›Full record

ArticlePediatric research2018

Development of severe bronchopulmonary dysplasia is associated with alterations in fecal volatile organic compounds.

Daniel J C Berkhout, Hendrik J Niemarkt, Marc A Benninga, Andries E Budding, Anton H van Kaam, Boris W Kramer, Charlene M Pantophlet, Mirjam M van Weissenbruch, Nanne K H de Boer, Tim G J de Meij

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In one paragraph

Article in Pediatric research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  6. Volatile organic compounds in exhaled breath of newborns: a pilot study.Journal of perinatology : official journal of the California Perinatal Association · 2025
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  13. Perinatal maternal antibiotic exposure augments lung injury in offspring in experimental bronchopulmonary dysplasia.American journal of physiology. Lung cellular and molecular physiology · 2020
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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

10 authors at 5 institutions in 1 country.

Daniel J C BerkhoutDepartment of Pediatric Gastroenterology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
Hendrik J NiemarktNeonatal Intensive Care Unit, Máxima Medical Center, Veldhoven, The Netherlands.
Marc A BenningaDepartment of Pediatric Gastroenterology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
Andries E BuddingDepartment of Microbiology, VU University Medical Center, Amsterdam, The Netherlands.
Anton H van KaamNeonatal Intensive Care Unit, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
Boris W KramerDepartment of Pediatrics, Maastricht University Medical Center, Maastricht, The Netherlands.
Charlene M PantophletDepartment of Pediatric Gastroenterology, VU University Medical Center, Amsterdam, The Netherlands.
Mirjam M van WeissenbruchNeonatal Intensive Care Unit, VU University Medical Center, Amsterdam, The Netherlands.
Nanne K H de BoerDepartment of Gastroenterology and Hepatology, VU University Medical Center, Amsterdam, The Netherlands.
Tim G J de MeijDepartment of Pediatric Gastroenterology, VU University Medical Center, Amsterdam, The Netherlands.
Amsterdam UMC Location VUmc · NLAcademic Medical Center · NLEmma Kinderziekenhuis · NLMaastricht University · NLMáxima Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundThe aim of this study was to evaluate the potential of fecal volatile organic compounds (VOCs), obtained by means of an electronic nose device (Cyranose 320), as early non-invasive biomarker for BPD.MethodsIn this nested case-control study performed at three Neonatal Intensive Care Units, fecal samples obtained at postnatal age of 7, 14, 21, and 28 days from preterm infants with severe bronchopulmonary dysplasia (BPD) were compared with fecal VOC profiles from matched controls. Microbiota analysis was performed by means of IS-pro technique on fecal samples collected at 28 days postnatally.ResultsVOC profiles of infants developing severe BPD (n=15) could be discriminated from matched controls (n=15) at postnatal age of 14 days (area under the curve (±95% confidence interval), P-value, sensitivity, specificity; 0.72 (0.54-0.90), 0.040, 60.0%, 73.3%), 21 days (0.71 (0.52-0.90), 0.049, 66.7%, 73.3%) and 28 days (0.77 (0.59-0.96), 0.017, 69.2%, 69.2%) but not at 7 days. Intestinal microbiota did not differ between BPD subjects and controls.ConclusionFecal VOC profiles of infants developing BPD could be differentiated from controls at postnatal day 14, 21, and 28. VOC differences could not be directed to intestinal microbiota alterations but presumably reflect local and systemic metabolic and inflammatory pathways associated with BPD.

Indexed as

Electronic NoseBiomarkersBronchopulmonary DysplasiaCase-Control StudiesFecesFemaleGastrointestinal MicrobiomeHumansInfant, NewbornInfant, PrematureIntensive Care Units, NeonatalMaleSensitivity and SpecificityTime FactorsVolatile Organic CompoundsBiomarkersVolatile Organic Compounds

Identifiers

PMID29053703
OpenAlexW2766485313

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.