Evidence map›Paper›PMID 31196444›Full record

ArticleProgress in brain research2019

Differential magnocellular versus parvocellular pathway contributions to the combinatorial processing of facial threat.

Reginald B Adams, Hee Yeon Im, Cody Cushing, Jasmine Boshyan, Noreen Ward, Daniel N Albohn, Kestutis Kveraga

Abstract read
In one paragraph

Article in Progress in brain research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. A deep neural network model of the primate superior colliculus for emotion recognition.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  3. 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

7 authors.

Reginald B AdamsDepartment of Psychology, The Pennsylvania State University, University Park, PA, United States. Electronic address: radams@psu.edu.
Hee Yeon ImAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, United States.
Cody CushingAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, United States.
Jasmine BoshyanAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, United States.
Noreen WardAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, United States.
Daniel N AlbohnDepartment of Psychology, The Pennsylvania State University, University Park, PA, United States.
Kestutis KveragaAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, United States.

Funding

Neurodynamics of Compound Threat Cue PerceptionR01MH101194 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI KVERAGA, KESTUTIS · 2014 to 2018
$3.7M
NIMH NIH HHS R01 MH101194
6 · The paper itself

Abstract

Recently, speed of presentation of facially expressive stimuli was found to influence the processing of compound threat cues (e.g., anger/fear/gaze). For instance, greater amygdala responses were found to clear (e.g., direct gaze anger/averted gaze fear) versus ambiguous (averted gaze anger/direct gaze fear) combinations of threat cues when rapidly presented (33 and 300ms), but greater to ambiguous versus clear threat cues when presented for more sustained durations (1, 1.5, and 2s). A working hypothesis was put forth (Adams et al., 2012) that these effects were due to differential magnocellular versus parvocellular pathways contributions to the rapid versus sustained processing of threat, respectively. To test this possibility directly here, we restricted visual stream processing in the fMRI environment using facially expressive stimuli specifically designed to bias visual input exclusively to the magnocellular versus parvocellular pathways. We found that for magnocellular-biased stimuli, activations were predominantly greater to clear versus ambiguous threat-gaze pairs (on par with that previously found for rapid presentations of threat cues), whereas activations to ambiguous versus clear threat-gaze pairs were greater for parvocellular-biased stimuli (on par with that previously found for sustained presentations). We couch these findings in an adaptive dual process account of threat perception and highlight implications for other dual process models within psychology.

Indexed as

Facial ExpressionAdultAmygdalaBrainCuesFearFemaleHumansMagnetic Resonance ImagingMaleNerve NetPhotic StimulationEye gazeFacial expressionFear expressionMagnocellularParvocellularShared signal hypothesisThreatThreat perceptionThreat-related ambiguity

Identifiers

PMID31196444
PMCPMC7395566

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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.