Evidence map›Paper›PMID 41249139›Full record

ArticleTranslational psychiatry2025

Perinatal brain growth and autistic traits in toddlers.

A Tsompanidis, K M Chang, Y T Khan, M A Radecki, L Dorschmidt, S Hampton, E Aydin, C Allison, R Tait, R A I Bethlehem and 5 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. 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

15 authors.

A TsompanidisAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK. at768@cam.ac.uk.ORCID http://orcid.org/0000-0002-7338-6536
K M ChangAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Y T KhanAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
M A RadeckiAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
L DorschmidtDepartment of Psychiatry and Lifespan Brain Institute, University of Pennsylvania, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-0447-1104
S HamptonYork Trials Unit, University of York, York, UK.
E AydinVagelos College of Physicians and Surgeons, Department of Psychiatry, Columbia University, Cambridge, USA.ORCID http://orcid.org/0000-0003-4845-053X
C AllisonAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
R TaitCambridge Open Zettascale Lab, University of Cambridge, Cambridge, UK.
R A I BethlehemDepartment of Psychology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-0714-0685
V KyriakopoulouDepartment of Early Life Imaging, School of Biomedical Engineering and Imaging Sciences, King's College London, St Thomas' Hospital, London, UK.ORCID http://orcid.org/0000-0002-9883-0314
T AustinNeoLab, Evelyn Perinatal Imaging Centre, Rosie Hospital, CUH NHS Trust, Cambridge, UK.
J SucklingPsychiatric Neuroimaging, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-5098-1527
R HoltAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
S Baron-CohenAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-9217-2544

Funding

Simons Foundation RNAG/669Wellcome Trust
6 · The paper itself

Abstract

Autism is a heterogeneous set of neurodevelopmental conditions with a significant heritable component and perinatal origins. The earliest observable behavioural traits, with which a diagnosis can be made, emerge at 18 months of age. Previous studies have reported increased head circumference and brain growth in autistic children, but less is known about whether this extends to the wider spectrum of traits or to early brain development in the first 6 months of life. Data from two independent cohorts, the developing Human Connectome Project (dHCP) and Cambridge Human Imaging and Longitudinal Development (CHILD), were assessed in late fetal and early infancy for brain structure with MRI. Global and regional brain volumes in the dHCP, were studied prenatally (n = 106, mean age = 29.27 [SD = 3.8] gestational weeks) and postnatally (n = 454, mean age = 41.28 [SD = 1.93] weeks post-conception) in association with later autistic traits after 18 months of age, as captured on the parent-report Quantitative Checklist for Autism in Toddlers ('Q-CHAT'). The results informed a region-of-interest analysis in the smaller independent CHILD cohort, where participants were scanned during pregnancy (mean = 31.98 weeks gestation, SD = 1.52) and postnatally (mean scan age = 50.45, SD = 2.8 weeks post-conception)(n = 27). After controlling for cohort covariates, such as maternal age, birth weight, sex and age post-conception at the time of scan, postnatal total brain volume, cortical grey matter volume, and white matter volume were all negatively associated with autistic traits in toddlerhood. This was found for postnatal volumes in both the dHCP and the CHILD cohort but was not apparent when assessing prenatal brain volume or perinatal growth rates of total brain volume in the same individuals. Regional analyses in the dHCP cohort, after controlling for total brain volume, showed patterns of note in the temporal lobe, which warrant further research. In conclusion, reduced total brain volume in the first two months of life is associated with a higher number of autistic traits, as reported by parents at 18 months of life. Further research is required to understand if this extends to later ages, to children later diagnosed with autism and how it affects the development and connectivity of specific regions, particularly in the temporal lobes.

Indexed as

Autistic DisorderBrainChild, PreschoolConnectomeFemaleHumansInfantInfant, NewbornLongitudinal StudiesMagnetic Resonance ImagingMaleOrgan SizePregnancy

Identifiers

PMID41249139
PMCPMC12623961

What OpenQuestion holds

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Registered trials

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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.