Evidence map›Paper›PMID 40800944›Full record

ArticleImaging neuroscience (Cambridge, Mass.)2025

Characterizing the temporal dynamics and maturation of brain activity during sleep: An EEG microstate study in preterm and full-term infants.

Parvaneh Adibpour, Hala Nasser, Amandine Pedoux, Laurie Devisscher, Nicolas Elbaz, Chloé Ghozland, Elodie Hinnekens, Sara Neumane, Claire Kabdebon, Aline Lefebvre and 10 more

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

20 authors.

Parvaneh AdibpourUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Hala NasserUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Amandine PedouxDepartment of Child and Adolescent Psychiatry, Robert-Debré University Hospital, APHP, Paris, France.
Laurie DevisscherUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Nicolas ElbazDepartment of Pediatric Radiology, Robert-Debré University Hospital, APHP, Paris, France.
Chloé GhozlandNeonatal Intensive Care Unit, Robert-Debré University Hospital, APHP, Paris, France.
Elodie HinnekensUniversité Paris Cité, CNRS, Integrative Neuroscience and Cognition Center, Paris, France.
Sara NeumaneUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Claire KabdebonUniversité Aix-Marseille, CNRS, Institute of Language, Communication and the Brain, Marseille, France.
Aline LefebvreDepartment of Child and Adolescent Psychiatry, Robert-Debré University Hospital, APHP, Paris, France.
Anna KaminskaUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Lucie Hertz-PannierUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Alice HeneauNeonatal Intensive Care Unit, Robert-Debré University Hospital, APHP, Paris, France.
Olivier SibonyDepartment of Gynecology-Obstetrics, Robert-Debré University Hospital, APHP, Paris, France.
Marianne AlisonUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Catherine DelanoëDepartment of Physiology-Functional Explorations, Robert-Debré University Hospital, Assistance Publique-Hôpitaux de Paris-APHP, Paris, France.
Richard DelormeDepartment of Child and Adolescent Psychiatry, Robert-Debré University Hospital, APHP, Paris, France.
Marianne Barbu-RothUniversité Paris Cité, CNRS, Integrative Neuroscience and Cognition Center, Paris, France.
Valérie BiranUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.
Jessica DuboisUniversité Paris Cité, INSERM, NeuroDiderot, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By interfering with the normal sequence of mechanisms serving the brain maturation, premature birth and related stress can alter perinatal experiences, with potential long-term consequences on a child's neurodevelopment. The early characterization of brain functioning and maturational changes is thus of critical interest in premature infants who are at high risk of atypical outcomes and could benefit from early diagnosis and dedicated interventions. Using high-density electroencephalography (HD-EEG), we recorded brain activity in extreme and very preterm infants at the equivalent age of pregnancy term (n = 43), and longitudinally 2 months later (n = 33), compared with full-term born infants (n = 14). We characterized the maturation of brain activity by using a dedicated microstate analysis to quantify the spatio-temporal dynamics of the spontaneous transient network activity while controlling for vigilance states. The comparison of premature and full-term infants first showed slower dynamics as well as altered spatio-temporal properties of brain activity in preterm infants. Maturation of functional networks between term-equivalent age and 2 months later in preterms was linked to the emergence of faster dynamics, manifested in part by shorter duration of microstates, as well as an evolution in the spatial organization of the dominant microstates. The inter-individual differences in the temporal dynamics of brain activity at term-equivalent age were further impacted by sex (with slower microstate dynamics in boys) and by gestational age at birth for some microstate dynamics but not by other considered risk factors. This study highlights the potential of the microstate approach to reveal maturational properties of the emerging brain network activity in premature infants.

Indexed as

brain developmentelectroencephalography (EEG)microstatesprematurityresting-state

Identifiers

PMID40800944
PMCPMC12319786

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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.