Evidence map›Paper›PMID 28736519›Full record

ArticleFrontiers in human neuroscience2017

Isolating Discriminant Neural Activity in the Presence of Eye Movements and Concurrent Task Demands.

Jon Touryan, Vernon J Lawhern, Patrick M Connolly, Nima Bigdely-Shamlo, Anthony J Ries

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 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

5 authors.

Jon TouryanU.S. Army Research Laboratory, Future Soldier Technologies Division, Human Research and Engineering Directorate, Aberdeen Proving GroundAberdeen, MD, United States.
Vernon J LawhernU.S. Army Research Laboratory, Future Soldier Technologies Division, Human Research and Engineering Directorate, Aberdeen Proving GroundAberdeen, MD, United States.
Patrick M ConnollyTeledyne Scientific CompanyDurham, NC, United States.
Nima Bigdely-ShamloQusp LabsSan Diego, CA, United States.
Anthony J RiesU.S. Army Research Laboratory, Future Soldier Technologies Division, Human Research and Engineering Directorate, Aberdeen Proving GroundAberdeen, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A growing number of studies use the combination of eye-tracking and electroencephalographic (EEG) measures to explore the neural processes that underlie visual perception. In these studies, fixation-related potentials (FRPs) are commonly used to quantify early and late stages of visual processing that follow the onset of each fixation. However, FRPs reflect a mixture of bottom-up (sensory-driven) and top-down (goal-directed) processes, in addition to eye movement artifacts and unrelated neural activity. At present there is little consensus on how to separate this evoked response into its constituent elements. In this study we sought to isolate the neural sources of target detection in the presence of eye movements and over a range of concurrent task demands. Here, participants were asked to identify visual targets (Ts) amongst a grid of distractor stimuli (Ls), while simultaneously performing an auditory N-back task. To identify the discriminant activity, we used independent components analysis (ICA) for the separation of EEG into neural and non-neural sources. We then further separated the neural sources, using a modified measure-projection approach, into six regions of interest (ROIs): occipital, fusiform, temporal, parietal, cingulate, and frontal cortices. Using activity from these ROIs, we identified target from non-target fixations in all participants at a level similar to other state-of-the-art classification techniques. Importantly, we isolated the time course and spectral features of this discriminant activity in each ROI. In addition, we were able to quantify the effect of cognitive load on both fixation-locked potential and classification performance across regions. Together, our results show the utility of a measure-projection approach for separating task-relevant neural activity into meaningful ROIs within more complex contexts that include eye movements.

Indexed as

cognitive loadEEGeye trackingfixation-related potentialstarget detection

Identifiers

PMID28736519
PMCPMC5501009

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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.