Evidence map›Paper›PMID 24806681›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Scale-free bursting in human cortex following hypoxia at birth.

James A Roberts, Kartik K Iyer, Simon Finnigan, Sampsa Vanhatalo, Michael Breakspear

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Symmetry breaking and avalanche shapes in modular neural networks.Frontiers in computational neuroscience · 2026
    Article
  2. Ephaptic coupling and power fluctuations in depression.bioRxiv : the preprint server for biology · 2025
    Article
  3. Maturation of Neuronal Activity in the Human Cortex Exhibits Robust Spatial Gradients across the Birth Transition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Bridge, Reverse Bridge, and Their Control.Entropy (Basel, Switzerland) · 2025
    Article
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  12. Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2021
    Article
  13. Automated cot-side tracking of functional brain age in preterm infants.Annals of clinical and translational neurology · 2020
    Article
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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

5 authors.

James A RobertsSystems Neuroscience Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland 4006, Australia, Faculty of Health Sciences, School of Medicine, University of Queensland, Brisbane, Queensland 4029, Australia, The University of Queensland Centre for Clinical Research and Perinatal Research Centre, Brisbane, Queensland 4006, Australia, Department of Children's Clinical Neurophysiology, Helsinki University Central Hospital and University of Helsinki, Helsinki HUS 00029, Finland, Royal Brisbane and Women's Hospital, Herston, Queensland 4006, Australia, and School of Psychiatry, University of New South Wales and The Black Dog Institute, Randwick, New South Wales 2031, Australia.
Kartik K Iyer
Simon Finnigan
Sampsa Vanhatalo
Michael Breakspear

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human brain is fragile in the face of oxygen deprivation. Even a brief interruption of metabolic supply at birth challenges an otherwise healthy neonatal cortex, leading to a cascade of homeostatic responses. During recovery from hypoxia, cortical activity exhibits a period of highly irregular electrical fluctuations known as burst suppression. Here we show that these bursts have fractal properties, with power-law scaling of burst sizes across a remarkable 5 orders of magnitude and a scale-free relationship between burst sizes and durations. Although burst waveforms vary greatly, their average shape converges to a simple form that is asymmetric at long time scales. Using a simple computational model, we argue that this asymmetry reflects activity-dependent changes in the excitatory-inhibitory balance of cortical neurons. Bursts become more symmetric following the resumption of normal activity, with a corresponding reorganization of burst scaling relationships. These findings place burst suppression in the broad class of scale-free physical processes termed crackling noise and suggest that the resumption of healthy activity reflects a fundamental reorganization in the relationship between neuronal activity and its underlying metabolic constraints.

Indexed as

AlgorithmsApgar ScoreAsphyxia NeonatorumCerebral CortexData Interpretation, StatisticalElectroencephalographyElectrophysiological PhenomenaFemaleGestational AgeHumansHydrogen-Ion ConcentrationInfant, NewbornLikelihood FunctionsMaleModels, NeurologicalModels, Statisticalburst suppressionEEGhypoxianeonatesneuronal avalanchesscale-free

Identifiers

PMID24806681
PMCPMC6608140

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.