Evidence map›Paper›PMID 30710356›Full record

ArticleEpilepsia2019

Four-dimensional functional cortical maps of visual and auditory language: Intracranial recording.

Yasuo Nakai, Ayaka Sugiura, Erik C Brown, Masaki Sonoda, Jeong-Won Jeong, Robert Rothermel, Aimee F Luat, Sandeep Sood, Eishi Asano

Abstract read
In one paragraph

Article in Epilepsia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Visualization of functional and effective connectivity underlying auditory descriptive naming.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Cortical and white matter substrates supporting visuospatial working memory.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Significance of event related causality (ERC) in eloquent neural networks.Neural networks : the official journal of the International Neural Network Society · 2022
    Article
  17. Article
  18. Article
  19. A distributed network supports spatiotemporal cerebral dynamics of visual naming.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2021
    Article
  20. Spontaneous modulations of high-frequency cortical activity.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2021
    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

9 authors.

Yasuo NakaiDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Ayaka SugiuraDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Erik C BrownDepartment of Neurological Surgery, Oregon Health and Science University, Portland, Oregon.
Masaki SonodaDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Jeong-Won JeongDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Robert RothermelDepartment of Psychiatry, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Aimee F LuatDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Sandeep SoodDepartment of Neurosurgery, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.
Eishi AsanoDepartment of Pediatrics, Detroit Medical Center, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan.ORCID 0000-0001-8391-4067

Funding

Functional brain mapping in pediatric neurosurgeryR01NS064033 · NINDS · WAYNE STATE UNIVERSITY · PI EISHI ASANO · 2009 to 2026
$5.7M
DEVELOPMENT OF MEMORY NETWORKS IN CHILDRENR01MH107512 · NIMH · WAYNE STATE UNIVERSITY · PI Noa Ofen · 2016 to 2026
$5.0M
Novel DWI Methods to Minimize Postoperative Deficits in Pediatric Epilepsy Surgery.R01NS089659 · NINDS · WAYNE STATE UNIVERSITY · PI JEONG, JEONG-WON · 2015 to 2025
$3.7M
Quantitative multimodal analyses in pediatric epilepsy surgeryK23NS047550 · NINDS · WAYNE STATE UNIVERSITY · PI ASANO, EISHI · 2004 to 2008
$768k
NIH HHS MH107512NIH HHS NS047550NIH HHS NS064033NIH HHS NS089659NIMH NIH HHS R01 MH107512NINDS NIH HHS K23 NS047550NINDS NIH HHS R01 NS064033NINDS NIH HHS R01 NS089659
6 · The paper itself

Abstract

objectiveThe strength of presurgical language mapping using electrocorticography (ECoG) is its outstanding signal fidelity and temporal resolution, but the weakness includes limited spatial sampling at an individual patient level. By averaging naming-related high-gamma activity at nonepileptic regions across a large number of patients, we provided the functional cortical atlases animating the neural dynamics supporting visual-object and auditory-description naming at the whole brain level.

methodsWe studied 79 patients who underwent extraoperative ECoG recording as epilepsy presurgical evaluation, and generated time-frequency plots and animation videos delineating the dynamics of naming-related high-gamma activity at 70-110 Hz.

resultsNaming task performance elicited high-gamma augmentation in domain-specific lower-order sensory areas and inferior-precentral gyri immediately after stimulus onset. High-gamma augmentation subsequently involved widespread neocortical networks with left hemisphere dominance. Left posterior temporal high-gamma augmentation at several hundred milliseconds before response onset exhibited a double dissociation; picture naming elicited high-gamma augmentation preferentially in regions medial to the inferior-temporal gyrus, whereas auditory naming elicited high-gamma augmentation more laterally. The left lateral prefrontal regions including Broca's area initially exhibited high-gamma suppression subsequently followed by high-gamma augmentation at several hundred milliseconds before response onset during both naming tasks. Early high-gamma suppression within Broca's area was more intense during picture compared to auditory naming. Subsequent lateral-prefrontal high-gamma augmentation was more intense during auditory compared to picture naming. SIGNIFICANCE: This study revealed contrasting characteristics in the spatiotemporal dynamics of naming-related neural modulations between tasks. The dynamic atlases of visual and auditory language might be useful for planning of epilepsy surgery. Differential neural activation well explains some of the previously reported observations of domain-specific language impairments following resective epilepsy surgery. Video materials might be beneficial for the education of lay people about how the brain functions differentially during visual and auditory naming.

Indexed as

LanguageAdolescentAdultBrainBrain MappingChildChild, PreschoolElectrocorticographyElectrodes, ImplantedElectroencephalographyEpilepsies, PartialEpilepsyFemaleHumansMaleYoung Adultevent-related high-gamma modulationfour-dimensional (4D)intracranial electroencephalography (iEEG) recordingphysiological high-frequency oscillations (HFOs)speech

Identifiers

PMID30710356
PMCPMC6365188

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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.