Evidence map›Paper›PMID 42447610›Full record

ArticleDevelopmental cognitive neuroscience2026

Characterization of aperiodic and theta activity in preterm infants using EEG: Insights into cerebral maturation and inter-individual variability.

Aline González Carpinteiro, Hala Nasser, Amandine Pedoux, Laurie Devisscher, Kunyan Cai, Nicolas Elbaz, Chloé Ghozland, Léa Guéret, Sara Neumane, Yann Leprince and 12 more

Abstract read
In one paragraph

Article in Developmental cognitive neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

22 authors.

Aline González CarpinteiroUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Hala NasserRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Functional Explorations, Paris F-75019, France.
Amandine PedouxRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Child and Adolescent Psychiatry, Paris F-75019, France.
Laurie DevisscherUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Kunyan CaiUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Nicolas ElbazRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Pediatric Radiology, Paris F-75019, France.
Chloé GhozlandRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Neonatal Intensive Care Unit, Paris F-75019, France.
Léa GuéretUniversity of Paris-Cité, CNRS, Integrative Neuroscience and Cognition Center, Paris F-75005, France.
Sara NeumaneUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Yann LeprinceUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Aline LefebvreRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Child and Adolescent Psychiatry, Paris F-75019, France.
Lucie Hertz-PannierUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France.
Alice HeneauRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Neonatal Intensive Care Unit, Paris F-75019, France.
Alice FrérotRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Neonatal Intensive Care Unit, Paris F-75019, France.
Olivier SibonyRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Gynecology-Obstetrics, Paris F-75019, France.
Catherine DelanoëRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Functional Explorations, Paris F-75019, France.
Marianne Barbu-RothUniversity of Paris-Cité, CNRS, Integrative Neuroscience and Cognition Center, Paris F-75005, France.
Marianne AlisonUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Robert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Pediatric Radiology, Paris F-75019, France.
Richard DelormeRobert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Department of Child and Adolescent Psychiatry, Paris F-75019, France.
Valérie BiranUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Robert-Debré Hospital, Assistance Publique-Hôpitaux de Paris - APHP, Neonatal Intensive Care Unit, Paris F-75019, France.
Jessica DuboisUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France. Electronic address: jessica.dubois@inserm.fr.
Parvaneh AdibpourUniversité Paris Cité, INSERM, NeuroDiderot, Paris F-75019, France; Université Paris Saclay, CEA, NeuroSpin, UNIACT, Gif-sur-Yvette F-91191, France; Centre for the Developing Brain, Department of Early Life Imaging, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preterm birth may disrupt maturation of brain networks and functional activity, including theta oscillations that play a key role in early network development. Traditional EEG spectral analyses show marked development of theta power in early infancy, but these approaches mix oscillatory and non-oscillatory activity, limiting insights into the underlying mechanisms. Using spectral parameterization, we assessed the development of aperiodic activity and periodic theta power in very preterm (born before 32 weeks gestational age, GA) and full-term infants, and examined inter-individual variability among preterms. High-density EEG was acquired during active/REM sleep at term-equivalent age (TEA) and 2 months corrected age (2mCA) in preterm (n = 41) and full-term (n = 13) infants. Spectral parameterization allowed extracting metrics of aperiodic activity (offset, exponent) and periodic theta power, globally and across spatial clusters of electrodes. From TEA to 2mCA, offset, exponent, and theta power increased with no differences between preterms and full-terms. At TEA, aperiodic activity metrics were stronger in anterior compared with posterior areas, but this regional landscape shifted by 2mCA due to pronounced changes in posterior areas from TEA to 2mCA. Within preterms, inter-individual variability in EEG metrics at TEA was partly explained by clinical risk factors (male sex, lower GA, being small for GA, and invasive ventilation) and variations in brain microstructure, as assessed with diffusion MRI: higher theta power correlated with more advanced cortical maturation. These findings indicate that EEG spectral parameterization combined with spatial analysis provides a sensitive framework for characterizing early brain maturation and vulnerabilities associated with prematurity.

Indexed as

Brain developmentDiffusion MRIElectroencephalographyPrematuritySpectral parameterization

Identifiers

PMID42447610
PMCPMC13382642

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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.