Evidence map›Paper›PMID 31156419›Full record

ArticleFrontiers in neurorobotics2019

Functional Source Separation for EEG-fMRI Fusion: Application to Steady-State Visual Evoked Potentials.

Hong Ji, Badong Chen, Nathan M Petro, Zejian Yuan, Nanning Zheng, Andreas Keil

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurorobotics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
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

6 citing papers in PubMed, 16 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Hong JiDepartment of Automation Science and Technology, Institute of Artificial Intelligence and Robotics, Xi'an Jiaotong University, Xi'an, China.
Badong ChenDepartment of Automation Science and Technology, Institute of Artificial Intelligence and Robotics, Xi'an Jiaotong University, Xi'an, China.
Nathan M PetroDepartment of Psychology, Center for Brain, Biology, and Behavior, University of Nebraska-Lincoln, Lincoln, NE, United States.
Zejian YuanDepartment of Automation Science and Technology, Institute of Artificial Intelligence and Robotics, Xi'an Jiaotong University, Xi'an, China.
Nanning ZhengDepartment of Automation Science and Technology, Institute of Artificial Intelligence and Robotics, Xi'an Jiaotong University, Xi'an, China.
Andreas KeilDepartment of Psychology, Center for the Study of Emotion and Attention, University of Florida, Gainesville, FL, United States.
Xi'an Jiaotong University · CNUniversity of Florida · USUniversity of Nebraska–Lincoln · US

Funding

MyAPS: Development and Validation of an AI Platform for Generating Emotional PicturesR01MH112558 · NIMH · UNIVERSITY OF FLORIDA · PI MINGZHOU DING, Ruogu Fang · 2017 to 2026
$2.5M
Acquisition and extinction of affective bias in perception: A single trial approaR01MH097320 · NIMH · UNIVERSITY OF FLORIDA · PI DING, MINGZHOU, KEIL, ANDREAS · 2012 to 2016
$1.7M
NIMH NIH HHS R01 MH097320NIMH NIH HHS R01 MH112558
6 · The paper itself

Abstract

Neurorobotics is one of the most ambitious fields in robotics, driving integration of interdisciplinary data and knowledge. One of the most productive areas of interdisciplinary research in this area has been the implementation of biologically-inspired mechanisms in the development of autonomous systems. Specifically, enabling such systems to display adaptive behavior such as learning from good and bad outcomes, has been achieved by quantifying and understanding the neural mechanisms of the brain networks mediating adaptive behaviors in humans and animals. For example, associative learning from aversive or dangerous outcomes is crucial for an autonomous system, to avoid dangerous situations in the future. A body of neuroscience research has suggested that the neurocomputations in the human brain during associative learning involve re-shaping of sensory responses. The nature of these adaptive changes in sensory processing during learning however are not yet well enough understood to be readily implemented into on-board algorithms for robotics application. Toward this overall goal, we record the simultaneous electroencephalogram (EEG) and functional magnetic resonance imaging (fMRI), characterizing one candidate mechanism, i.e., large-scale brain oscillations. The present report examines the use of Functional Source Separation (FSS) as an optimization step in EEG-fMRI fusion that harnesses timing information to constrain the solutions that satisfy physiological assumptions. We applied this approach to the voxel-wise correlation of steady-state visual evoked potential (ssVEP) amplitude and blood oxygen level-dependent imaging (BOLD), across both time series. The results showed the benefit of FSS for the extraction of robust ssVEP signals during simultaneous EEG-fMRI recordings. Applied to data from a 3-phase aversive conditioning paradigm, the correlation maps across the three phases (habituation, acquisition, extinction) show converging results, notably major overlapping areas in both primary and extended visual cortical regions, including calcarine sulcus, lingual cortex, and cuneus. In addition, during the acquisition phase when aversive learning occurs, we observed additional correlations between ssVEP and BOLD in the anterior cingulate cortex (ACC) as well as the precuneus and superior temporal gyrus.

Indexed as

aversive conditioningfunctional source separation (FSS)simulated annealing (SA)simultaneous EEG and fMRIsteady-state visual evoked potentials (ssVEP)

Identifiers

PMID31156419
PMCPMC6528067
OpenAlexW2945541133

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.