Evidence map›Paper›PMID 40706725›Full record

ArticleNeuroImage2025

Developmental trajectory of neural activity underlying motor control differs by sequence complexity and motor stage.

Thomas W Ward, Jackson Derby, Jake J Son, Peihan J Huang, Danielle L Rice, Grace C Ende, Anna T Coutant, Erica L Steiner, Vince D Calhoun, Yu-Ping Wang and 3 more

Abstract read
In one paragraph

Article in NeuroImage, 2025. 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. Article
  2. Article
  3. Review
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

13 authors.

Thomas W WardInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, USA.
Jackson DerbyInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Jake J SonInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA; College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Peihan J HuangInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Danielle L RiceInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Grace C EndeInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Anna T CoutantInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Erica L SteinerInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA.
Vince D CalhounTri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, and Emory University, Atlanta, GA, USA.
Yu-Ping WangDepartment of Biomedical Engineering, Tulane University, New Orleans, LA, USA.
Julia M StephenMind Research Network, Albuquerque, NM, USA.
Elizabeth Heinrichs-GrahamInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, USA.
Tony W WilsonInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, USA; College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA. Electronic address: tony.wilson@boystown.org.

Funding

Stress-Induced Aberrations in the Mitochondrial Redox Environment Impact Developing Neural Circuits Supporting Cognitive ControlP20GM144641 · NIGMS · FATHER FLANAGAN'S BOYS' HOME · PI Rachel K. Spooner · 2022 to 2026
$15.1M
DEVELOPMENTAL MULTIMODAL IMAGING OF NEUROCOGNITIVE DYNAMICS (DEV-MIND)R01MH121101 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WILSON, TONY W · 2019 to 2023
$5.8M
Impact of Trauma on the Longitudinal Development of Cognitive Control Networks in Healthy YouthF30MH134713 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Jake Son · 2023 to 2026
$196k
NIGMS NIH HHS P20 GM144641NIMH NIH HHS F30 MH134713NIMH NIH HHS R01 MH121101
6 · The paper itself

Abstract

Primary motor areas in the brain mature relatively early in development, yet the control of complex movements improves through early adulthood. Neural oscillations in higher-order regions are refined in adolescence and contribute to executive processes important for complex motor control, but the neural dynamics among these regions and primary motor cortices remain poorly understood in youth. We recorded magnetoencephalography during a motor sequencing task in 68 healthy youth from ten to 17 years of age. Significant changes in oscillatory activity relative to baseline were identified at the sensor level and source reconstructed with a beamformer. Whole-brain maps of beta (18-24 Hz) and gamma (74-84 Hz) oscillatory activity were subjected to voxel-wise repeated-measures ANCOVAs to identify brain areas in which the developmental trajectory of oscillatory power differed by sequence complexity (simple/complex) or motor stage (planning/execution). Beta activity in bilateral prefrontal cortices was weaker with age during the planning of complex movements. Across simple and complex conditions, older youth tended to have stronger beta in posterior areas during planning. Finally, gamma activity across conditions was stronger with age in occipital and weaker in temporal cortices. These results suggest that the functional refinement of association cortices may drive improvements in motor control by enabling more efficient attentional and inhibitory control during formulation of the motor plan.

Indexed as

Motor CortexPsychomotor PerformanceAdolescentBeta RhythmBrain MappingChildFemaleGamma RhythmHumansMagnetoencephalographyMaleBetaDevelopmentERDGammaMagnetoencephalographyMEGOscillations

Identifiers

PMID40706725
PMCPMC12426476

What OpenQuestion holds

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LicenceCC BY-NC
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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.