Evidence map›Paper›PMID 41540202›Full record

ArticlePediatric research2026

Investigating the influence of maternal prenatal BMI and perinatal depressive symptoms on neonatal brain network dynamics.

Isabella L C Mariani Wigley, Alexandra Lautarescu, Elena Vartiainen, Elmo P Pulli, Niloofar Hashempour, Harri Merisaari, Wajiha Bano, Silja Luotonen, Ashmeet Jolly, Ilkka Suuronen and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 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. Review
  2. Review
  3. 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

17 authors.

Isabella L C Mariani WigleyFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland. ilmawi@utu.fi.ORCID http://orcid.org/0000-0003-0958-5124
Alexandra LautarescuDepartment of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Elena VartiainenFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Elmo P PulliFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Niloofar HashempourFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Harri MerisaariFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Wajiha BanoFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Silja LuotonenFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Ashmeet JollyFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Ilkka SuuronenFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Linnea KarlssonFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Hasse KarlssonFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.
Joana CabralCentre for Eudaimonia and Human Flourishing, Linacre College, University of Oxford, Oxford, UK.
Morten L KringelbachCentre for Eudaimonia and Human Flourishing, Linacre College, University of Oxford, Oxford, UK.
Dafnis BatalleEarly Life Imaging Research Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
A David EdwardsEarly Life Imaging Research Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
Jetro J TuulariFinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku and Turku University Hospital, Turku, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElevated pre-pregnancy body mass index (BMI) and perinatal depressive symptoms have been linked to neonatal alterations in brain structure and function. This study examined associations between neonatal functional brain dynamics, maternal BMI, and perinatal depressive symptoms measured by the Edinburgh Postnatal Depression Scale (EPDS) in a community-based, largely low-risk cohort.

methodsFuncitonal MRI and Leading Eigenvector Analysis (LEiDA) were applied in a neonatal cohort (N = 437; 236 males; mean gestational age 39.6 weeks) from the developing Human Connectome Project. We assessed whether neonatal brain-state probabilities related to maternal BMI and EPDS scores (M = 5.6, SD = 4.3), testing main effects and, separately, their interaction. The sample included 291 healthy-weight (BMI < 25), 98 overweight (25 BMI < 30), and 48 obese (BMI 30) mothers.

resultsEPDS scores were low in this cohort and did not demonstrate associations with brain states or a significant BMI × EPDS interaction. Higher maternal pre-pregnancy BMI was negatively associated with the stability of a functional network encompassing superior frontal, superior parietal, and temporal regions (ß = -0.129, p = 0.006).

conclusionAs this network is normally recruited more with age, reduced stability suggests slowed maturation of fronto-parieto-temporal systems and may signal early risk for later behavioral challenges. IMPACT: Higher maternal pre-pregnancy BMI is associated with reduced stability in a neonatal frontoparietal brain state, characterized by coordinated activity in frontal, parietal, and temporal regions. This state is one of six distinct dynamic connectivity patterns identified, reflecting core neonatal resting-state networks. The association was robust across multiple analytic models and clustering solutions. No significant effects were found for maternal depressive symptoms. These findings underscore the selective impact of maternal metabolic health on early brain organization, suggesting prenatal influences on the functional architecture of the newborn brain that may shape long-term neurodevelopmental trajectories.

Identifiers

What Socratic 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 Socratic graph.