Evidence map›Paper›PMID 41453123›Full record

Observational studyNeurology2026

Whole-Brain Dynamic Causal Tractography Atlas of Auditory and Visual Speech Networks Derived From Intracranial Neurophysiologic Data.

Ryuzaburo Kochi, Aya Kanno, Hiroshi Uda, Keisuke Hatano, Hidenori Endo, Michael Cools, Robert Rothermel, Aimee F Luat, Eishi Asano

Abstract readObservational Study
In one paragraph

Observational study in Neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

9 authors.

Ryuzaburo KochiDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.ORCID 0009-0008-4462-1710
Aya KannoDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.
Hiroshi UdaDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.ORCID 0000-0002-7814-697X
Keisuke HatanoDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.
Hidenori EndoDepartment of Neurosurgery, Tohoku University, Sendai, Miyagi, Japan.ORCID 0000-0003-1472-6032
Michael CoolsDepartment of Neurosurgery, Children's Hospital of Michigan, Detroit Medical Center.
Robert RothermelDepartment of Psychiatry, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.
Aimee F LuatDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.ORCID 0000-0002-1235-0708
Eishi AsanoDepartment of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit Medical Center.ORCID 0000-0001-8391-4067

Funding

Functional brain mapping in pediatric neurosurgeryR01NS064033 · NINDS · WAYNE STATE UNIVERSITY · PI EISHI ASANO · 2009 to 2026
$5.7M
NINDS NIH HHS R01 NS064033
6 · The paper itself

Abstract

BACKGROUND AND

objectivesSince Penfield's era, invasive neurophysiology has laid a lasting foundation for functional neuroscience by elucidating brain regions necessary for speech. Yet, whole-brain studies have not distinguished the millisecond-scale dynamics and specific white matter pathways that support rapid naming in the auditory and visual domains. We developed a whole-brain dynamic causal tractography atlas of speech using intracranial neurophysiologic data.

methodsThis observational study analyzed intracranial EEG during naming tasks in patients with drug-resistant focal epilepsy who underwent epilepsy surgery at Detroit Medical Center, MI. Task-related cortical high-gamma modulations were quantified, and functional coactivation was defined as sustained high-gamma augmentation occurring simultaneously in cortical regions directly connected by a white matter tract. We examined high-gamma modulations and functional coactivation associated with rapid and delayed auditory and picture naming responses. Electrical stimulation tested the causal significance of these dynamics.

resultsA total of 125 patients (5-49 years; 61 female patients) were included. The atlas revealed white matter coactivation intensity patterns at specific 5-millisecond time windows that best aligned with sensorimotor and language symptoms elicited by electrical stimulation. Rapid auditory naming was associated with deactivation of the right rostral middle frontal gyrus and increased coactivation along the left arcuate fasciculus, linked to stimulation-induced receptive and expressive aphasia. By contrast, delayed auditory naming correlated with a late surge in bifrontal coactivation. Rapid picture naming involved early coactivation between cortices connected through the bilateral inferior longitudinal fasciculi-associated with stimulation-induced visual distortions-coinciding with transient co-deactivation of the Broca area. Left-handedness and left-hemispheric epileptogenicity were associated with reduced left-hemispheric dominant high-gamma augmentation in specific regions. DISCUSSION: These findings delineate dissociable white matter-mediated mechanisms, supporting rapid naming in auditory and visual domains. Reduced inhibitory monitoring by the right dorsolateral prefrontal cortex may facilitate efficient lexical retrieval through left perisylvian pathways during auditory naming, whereas excessive bifrontal interaction may underlie delayed auditory naming. Rapid visual object recognition seems to rely on early occipito-temporal coactivation with minimal Broca area involvement. The resulting atlas provides a resource for trainees studying the network dynamics underlying speech and for presurgical language mapping in patients undergoing cortical or subcortical interventions.

Indexed as

BrainSpeechAdolescentAdultBrain MappingChildChild, PreschoolDiffusion Tensor ImagingDrug Resistant EpilepsyElectrocorticographyEpilepsies, PartialFemaleHumansMaleMiddle AgedNerve Net

Identifiers

PMID41453123
PMCPMC12746732

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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.