Evidence map›Paper›PMID 42158375›Full record

ArticleFrontiers in pediatrics2026

Brain activity as a candidate biomarker for personalised caffeine treatment in premature neonates.

Fatima Usman, Coen S Zandvoort, Shellie Robinson, Mariska Peck, Maria M Cobo, Tricia Adjei, Luke Baxter, Ria Evans Fry, Annalisa G V Hauck, Richard Rogers and 7 more

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. Review
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

17 authors.

Fatima Usman *Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Coen S Zandvoort *Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Shellie RobinsonDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Mariska PeckDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Maria M CoboDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Tricia AdjeiDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Luke BaxterDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Ria Evans FryDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Annalisa G V HauckDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Richard RogersNuffield Division of Anaesthetics, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
Gabriela Schmidt MelladoDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Alexandra ScrivensDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Marianne van der VaartDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Maarten De VosDepartment of Electrical Engineering (ESAT), STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven, Leuven, Belgium.
Eleri AdamsNewborn Care Unit, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
John van den AnkerDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.
Caroline HartleyDepartment of Paediatrics, University of Oxford, Oxford, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Caffeine is one of the most frequently administered medicines in neonatology-prescribed for the management of apnoea of prematurity, to aid extubation and increasingly for conditions such as bronchopulmonary dysplasia. Caffeine guidelines for the management of apnoea of prematurity indicate use based on the age of the infant, but this does not account for individual variation in apnoea rate. Consequently, infants may risk caffeine undertreatment or adverse events due to over-exposure. Apnoea in preterm infants is related to nervous system immaturity, hence, as an essential first step to assess whether brain activity may be a useful biomarker for caffeine treatment, we tested the hypothesis that apnoea rate is related to brain activity. Methods: In this single-centre prospective observational cohort study, we simultaneously recorded brain activity using electroencephalography (EEG) and respiration using impedance pneumography in 74 infants aged 31-36 weeks postmenstrual age (PMA) on 138 separate occasions. The primary outcome was the association between apnoea rate and brain age gap (defined as the difference between the infant's brain age and their PMA; brain age is calculated from brain activity using a deep learning algorithm). In an exploratory sub-study, we compared the apnoea and desaturation rate in the 7 days after infants stopped caffeine treatment, between those infants with immature and mature brain activity. Results: We demonstrate that apnoea rate in moderate/late preterm infants is dependent on brain age gap (p:0.024; Conclusions: These findings provide initial evidence to indicate that brain age is a candidate biomarker for personalised caffeine treatment in preterm infants.

Indexed as

apnoea of prematuritybrain agecaffeineEEGneonate

Identifiers

PMID42158375
PMCPMC13180734

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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.