Evidence map›Paper›PMID 39818327›Full record

ArticleBiological psychiatry2025

Sex Differences in the Striatal Contributions to Longitudinal Fine Motor Development in Autistic Children.

Olivia Surgent, Derek S Andrews, Joshua K Lee, Joseph Boyle, Andrew Dakopolos, Meghan Miller, Sally Ozonoff, Sally J Rogers, Marjorie Solomon, David G Amaral and 1 more

Abstract read
In one paragraph

Article in Biological psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

11 authors.

Olivia SurgentMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California. Electronic address: osurgent@ucdavis.edu.
Derek S AndrewsMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Joshua K LeeMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Joseph BoyleMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California; Department of Psychology, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Andrew DakopolosMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Meghan MillerMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Sally OzonoffMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Sally J RogersMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Marjorie SolomonMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
David G AmaralMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.
Christine Wu NordahlMIND Institute and Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, University of California, Davis, Sacramento, California.

Funding

Research Project: Pathologic Significance of Maternal AutoantibodiesP50HD103526 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEONARD J. ABBEDUTO, Melissa Dawn Bauman · 2020 to 2026
$9.7M
Interdisciplinary Training for Autism Researchers(RMI)T32MH073124 · NIMH · UNIVERSITY OF CALIFORNIA DAVIS · PI Stephen Charles Noctor, Christine Wu Nordahl · 2004 to 2026
$6.8M
Neural and developmental trajectories of females with autism spectrum disorderR01MH127046 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Christine Wu Nordahl · 2022 to 2026
$3.8M
NICHD NIH HHS P50 HD103526NIMH NIH HHS R01 MH127046NIMH NIH HHS T32 MH073124
6 · The paper itself

Abstract

backgroundFine motor challenges are prevalent in autistic populations. However, little is known about their neurobiological underpinnings or how their related neural mechanisms are influenced by sex. The dorsal striatum, which comprises the caudate nucleus and putamen, is associated with motor learning and control and may hold critical information. We investigated how autism diagnosis and sex assigned at birth influence associations between the dorsal striatum and fine motor development in autistic and nonautistic children.

methodsWe used multimodal assessment of striatal structures (volume and corticostriatal white matter microstructure) and longitudinal assessment of fine motor skills, first at approximately 3 years of age (time 1) and again 2 to 3 years later (follow-up). Fine motor and magnetic resonance imaging (T1 and diffusion) data were collected at time 1 from 356 children (234 autistic; 128 girls) and at follow-up from 195 children (113 autistic; 76 girls).

resultsAt time 1, associations among fine motor skills, putamen volume, and sensorimotor-striatal fractional anisotropy (sensorimotor-affiliated dorsal striatal structures) were different in autistic boys compared with autistic girls and were not significant for nonautistic children. Further, time 1 sensorimotor-striatal and prefrontal-striatal microstructure predicted fine motor development for autistic girls but not boys.

conclusionsSensorimotor-affiliated dorsal striatum structures may contribute to concurrent motor ability and predict fine motor improvement during critical windows of development in a sex-specific and diagnosis-dependent way. Moreover, the dorsal striatum may play a key role in the distinct neural mechanisms underlying motor challenges in autistic boys and girls.

Indexed as

Autistic DisorderChild DevelopmentCorpus StriatumMotor SkillsSex CharacteristicsChild, PreschoolFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMalePutamenWhite MatterCaudateFemalesPutamenSensoryVolumeWhite matter

Identifiers

PMID39818327
PMCPMC12124950

What OpenQuestion holds

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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.