Evidence map›Paper›PMID 38537603›Full record

ArticleEBioMedicine2024

A growth chart of brain function from infancy to adolescence based on EEG.

Kartik K Iyer, James A Roberts, Michaela Waak, Simon J Vogrin, Ajay Kevat, Jasneek Chawla, Leena M Haataja, Leena Lauronen, Sampsa Vanhatalo, Nathan J Stevenson

Abstract read
In one paragraph

Article in EBioMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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.

Kartik K IyerBrain Modelling Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia; Faculty of Medicine, The University of Queensland, Brisbane, Australia. Electronic address: Kartik.Iyer@qimrberghofer.edu.au.
James A RobertsBrain Modelling Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Michaela WaakFaculty of Medicine, The University of Queensland, Brisbane, Australia; Queensland Children's Hospital, Brisbane, Australia.
Simon J VogrinSt Vincent's Hospital, Melbourne, Australia.
Ajay KevatFaculty of Medicine, The University of Queensland, Brisbane, Australia; Queensland Children's Hospital, Brisbane, Australia.
Jasneek ChawlaFaculty of Medicine, The University of Queensland, Brisbane, Australia; Queensland Children's Hospital, Brisbane, Australia.
Leena M HaatajaDepartments of Physiology and Clinical Neurophysiology, BABA Center, Paediatric Research Center, Children's Hospital, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Leena LauronenDepartments of Physiology and Clinical Neurophysiology, BABA Center, Paediatric Research Center, Children's Hospital, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Sampsa VanhataloDepartments of Physiology and Clinical Neurophysiology, BABA Center, Paediatric Research Center, Children's Hospital, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Nathan J StevensonBrain Modelling Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia. Electronic address: Nathan.Stevenson@qimrberghofer.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn children, objective, quantitative tools that determine functional neurodevelopment are scarce and rarely scalable for clinical use. Direct recordings of cortical activity using routinely acquired electroencephalography (EEG) offer reliable measures of brain function.

methodsWe developed and validated a measure of functional brain age (FBA) using a residual neural network-based interpretation of the paediatric EEG. In this cross-sectional study, we included 1056 children with typical development ranging in age from 1 month to 18 years. We analysed a 10- to 15-min segment of 18-channel EEG recorded during light sleep (N1 and N2 states).

findingsThe FBA had a weighted mean absolute error (wMAE) of 0.85 years (95% CI: 0.69-1.02; n = 1056). A two-channel version of the FBA had a wMAE of 1.51 years (95% CI: 1.30-1.73; n = 1056) and was validated on an independent set of EEG recordings (wMAE = 2.27 years, 95% CI: 1.90-2.65; n = 723). Group-level maturational delays were also detected in a small cohort of children with Trisomy 21 (Cohen's d = 0.36, p = 0.028).

interpretationA FBA, based on EEG, is an accurate, practical and scalable automated tool to track brain function maturation throughout childhood with accuracy comparable to widely used physical growth charts.

fundingThis research was supported by the National Health and Medical Research Council, Australia, Helsinki University Diagnostic Center Research Funds, Finnish Academy, Finnish Paediatric Foundation, and Sigrid Juselius Foundation.

Indexed as

BrainGrowth ChartsAdolescentChildCross-Sectional StudiesElectroencephalographyHumansNeural Networks, ComputerBrain ageBrain functionEEGMachine learningNeurodevelopmentPaediatric

Identifiers

PMID38537603
PMCPMC11026939

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.