Evidence map›Paper›PMID 38955488›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2024

Conflicting Sensory Information Sharpens the Neural Representations of Early Selective Visuospatial Attention.

Panchalee Sookprao, Kanyarat Benjasupawan, Tanagrit Phangwiwat, Itthi Chatnuntawech, Kanda Lertladaluck, Angela Gutchess, Chaipat Chunharas, Sirawaj Itthipuripat

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  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

8 authors.

Panchalee SookpraoNeuroscience Center for Research and Innovation (NX), Learning Institute, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.ORCID 0009-0003-7937-6827
Kanyarat BenjasupawanNeuroscience Center for Research and Innovation (NX), Learning Institute, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.ORCID 0000-0002-3039-0623
Tanagrit PhangwiwatNeuroscience Center for Research and Innovation (NX), Learning Institute, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.
Itthi ChatnuntawechNational Nanotechnology Center, National Science and Technology Development Agency, Pathum Thani 12120, Thailand.ORCID 0000-0002-4049-5648
Kanda LertladaluckNeuroscience Center for Research and Innovation (NX), Learning Institute, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.ORCID 0000-0001-9437-3841
Angela GutchessDepartment of Psychology, Neuroscience Program, Volen National Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02453.ORCID 0000-0003-3047-5907
Chaipat ChunharasChula Neuroscience Center, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok 10330, Thailand itthipuripat.sirawaj@gmail.com chaipat.c@chula.ac.th.ORCID 0000-0003-1074-0160
Sirawaj ItthipuripatNeuroscience Center for Research and Innovation (NX), Learning Institute, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand itthipuripat.sirawaj@gmail.com chaipat.c@chula.ac.th.ORCID 0000-0001-9302-0964

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptive behaviors require the ability to resolve conflicting information caused by the processing of incompatible sensory inputs. Prominent theories of attention have posited that early selective attention helps mitigate cognitive interference caused by conflicting sensory information by facilitating the processing of task-relevant sensory inputs and filtering out behaviorally irrelevant information. Surprisingly, many recent studies that investigated the role of early selective attention on conflict mitigation have failed to provide positive evidence. Here, we examined changes in the selectivity of early visuospatial attention in male and female human subjects performing an attention-cueing Eriksen flanker task, where they discriminated the shape of a visual target surrounded by congruent or incongruent distractors. We used the inverted encoding model to reconstruct spatial representations of visual selective attention from the topographical patterns of amplitude modulations in alpha band oscillations in scalp EEG (∼8-12 Hz). We found that the fidelity of the alpha-based spatial reconstruction was significantly higher in the incongruent compared with the congruent condition. Importantly, these conflict-related modulations in the reconstruction fidelity occurred at a much earlier time window than those of the lateralized posterior event-related potentials associated with target selection and distractor suppression processes, as well as conflict-related modulations in the frontocentral negative-going wave and midline-frontal theta oscillations (∼3-7 Hz), thought to track executive control functions. Taken together, our data suggest that conflict resolution is supported by the cascade of neural processes underlying early selective visuospatial attention and frontal executive functions that unfold over time.

Indexed as

AttentionSpace PerceptionVisual PerceptionAdultConflict, PsychologicalCuesElectroencephalographyEvoked PotentialsFemaleHumansMalePhotic StimulationYoung Adultalphaattentioncognitive controlconflictEEGinverted encoding model

Identifiers

PMID38955488
PMCPMC11326869

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.