Evidence map›Paper›PMID 36344694›Full record

ArticlePediatric research2023

Bronchopulmonary dysplasia is not related to neurofilament light for neuroaxonal damage in preterm infants.

Michelle Romijn, Emma M Baas, Birgit I Lissenberg-Witte, Wes Onland, Marsh Königs, Jaap Oosterlaan, Hans Heijst, Joost Rotteveel, Anton H van Kaam, Charlotte E Teunissen and 1 more

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In one paragraph

Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 76% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 3 institutions in 1 country.

Michelle RomijnDepartment of Pediatric Endocrinology, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands. m.romijn1@amsterdamumc.nl.ORCID http://orcid.org/0000-0003-3558-554X
Emma M BaasDepartment of Pediatric Endocrinology, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Birgit I Lissenberg-WitteDepartment of Epidemiology and Data Science, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Wes OnlandDepartment of Neonatology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Marsh KönigsEmma Neuroscience Group, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Jaap OosterlaanDepartment of Pediatrics, Emma Children's Hospital Amsterdam UMC Follow-Me program & Emma Neuroscience Group, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Hans HeijstNeurochemistry Laboratory, Department of Clinical Chemistry Amsterdam Neuroscience, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Joost RotteveelDepartment of Pediatric Endocrinology, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Anton H van KaamDepartment of Neonatology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Charlotte E TeunissenNeurochemistry Laboratory, Department of Clinical Chemistry Amsterdam Neuroscience, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Martijn J J FinkenDepartment of Pediatric Endocrinology, Amsterdam UMC location Vrije Universiteit Amsterdam, Boelelaan 1117, Amsterdam, the Netherlands.
Amsterdam University Medical Centers · NLAmsterdam Neuroscience · NLEmma Kinderziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurofilament light (NfL) has been identified as a biomarker for neuroaxonal damage in preterm infants, but its relation with bronchopulmonary dysplasia (BPD) has not been established. We hypothesized that BPD is associated with increased NfL levels at an early stage, indicative of early neuroaxonal damage.

methodsWe included preterm infants born <30 weeks of gestation for assessment of NfL levels from cord blood and blood obtained at postnatal days 3, 7, 14, and 28. We used linear regression analysis to compare NfL levels between infants with moderate/severe BPD and infants with no/mild BPD, and linear mixed model analysis to compare the effect of time on NfL levels between groups.

resultsSixty-seven infants with a gestational age (GA) of 27 ± 1.3 weeks were included for analysis, of whom 19 (28%) developed moderate/severe BPD. Although NfL levels were higher at every time point in infants with BPD, statistical significance was lost after adjustment for GA, small for gestational age (SGA) and intraventricular hemorrhage (IVH). Groups did not differ in NfL change over time.

conclusionsThe positive association between BPD and NfL in the first weeks of life could be explained by GA, SGA and IVH rather than by development of BPD. IMPACT: Neurofilament light chain (NfL) is a known biomarker for neuroaxonal damage. Biomarkers for brain damage during the first weeks of life in preterm infants developing BPD are lacking. NfL levels obtained during the first weeks of life did not differ between infants with and without BPD in analyses adjusted for GA, SGA, and IVH.

Indexed as

Bronchopulmonary DysplasiaInfant, PrematureBiomarkersCerebral HemorrhageGestational AgeHumansInfantInfant, NewbornIntermediate FilamentsBiomarkers

Identifiers

PMID36344694
OpenAlexW4308453963

What OpenQuestion holds

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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.