Evidence map›Paper›PMID 33192393›Full record

ArticleFrontiers in human neuroscience2020

Mapping the Scene and Object Processing Networks by Intracranial EEG.

Kamil Vlcek, Iveta Fajnerova, Tereza Nekovarova, Lukas Hejtmanek, Radek Janca, Petr Jezdik, Adam Kalina, Martin Tomasek, Pavel Krsek, Jiri Hammer and 1 more

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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.

Kamil VlcekDepartment of Neurophysiology of Memory, Institute of Physiology, Czech Academy of Sciences, Prague, Czechia.
Iveta FajnerovaDepartment of Neurophysiology of Memory, Institute of Physiology, Czech Academy of Sciences, Prague, Czechia.
Tereza NekovarovaDepartment of Neurophysiology of Memory, Institute of Physiology, Czech Academy of Sciences, Prague, Czechia.
Lukas HejtmanekDepartment of Neurophysiology of Memory, Institute of Physiology, Czech Academy of Sciences, Prague, Czechia.
Radek JancaDepartment of Circuit Theory, Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czechia.
Petr JezdikDepartment of Circuit Theory, Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czechia.
Adam KalinaDepartment of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.
Martin TomasekDepartment of Neurosurgery, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.
Pavel KrsekDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.
Jiri HammerDepartment of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.
Petr MarusicDepartment of Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czechia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human perception and cognition are based predominantly on visual information processing. Much of the information regarding neuronal correlates of visual processing has been derived from functional imaging studies, which have identified a variety of brain areas contributing to visual analysis, recognition, and processing of objects and scenes. However, only two of these areas, namely the parahippocampal place area (PPA) and the lateral occipital complex (LOC), were verified and further characterized by intracranial electroencephalogram (iEEG). iEEG is a unique measurement technique that samples a local neuronal population with high temporal and anatomical resolution. In the present study, we aimed to expand on previous reports and examine brain activity for selectivity of scenes and objects in the broadband high-gamma frequency range (50-150 Hz). We collected iEEG data from 27 epileptic patients while they watched a series of images, containing objects and scenes, and we identified 375 bipolar channels responding to at least one of these two categories. Using K-means clustering, we delineated their brain localization. In addition to the two areas described previously, we detected significant responses in two other scene-selective areas, not yet reported by any electrophysiological studies; namely the occipital place area (OPA) and the retrosplenial complex. Moreover, using iEEG we revealed a much broader network underlying visual processing than that described to date, using specialized functional imaging experimental designs. Here, we report the selective brain areas for scene processing include the posterior collateral sulcus and the anterior temporal region, which were already shown to be related to scene novelty and landmark naming. The object-selective responses appeared in the parietal, frontal, and temporal regions connected with tool use and object recognition. The temporal analyses specified the time course of the category selectivity through the dorsal and ventral visual streams. The receiver operating characteristic analyses identified the PPA and the fusiform portion of the LOC as being the most selective for scenes and objects, respectively. Our findings represent a valuable overview of visual processing selectivity for scenes and objects based on iEEG analyses and thus, contribute to a better understanding of visual processing in the human brain.

Indexed as

high-frequency gamma activityhuman brainlateral occipital complexobjectsparahippocampal place areascenesstereoencephalographyvisual processing

Identifiers

PMID33192393
PMCPMC7581859

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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.