Evidence map›Paper›PMID 26653995›Full record

ArticleBMC neuroscience2015

Neurophysiological modulation of rapid emotional face processing is associated with impulsivity traits.

Takahiro Soshi, Takamasa Noda, Kumiko Ando, Kanako Nakazawa, Hideki Tsumura, Takayuki Okada

Abstract read
In one paragraph

Article in BMC neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Post-error slowing in anxiety and obsessive-compulsive disorders.Cognitive, affective & behavioral neuroscience · 2022
    Article
  4. Article
  5. 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

6 authors.

Takahiro SoshiDepartment of Forensic Psychiatry, National Center of Neurology and Psychiatry, National Institute of Mental Health, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8553, Japan. soshi@ncnp.go.jp.
Takamasa NodaDepartment of Psychiatry, National Center Hospital, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8551, Japan. t-noda@ncnp.go.jp.
Kumiko AndoDepartment of Forensic Psychiatry, National Center of Neurology and Psychiatry, National Institute of Mental Health, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8553, Japan. ando@ncnp.go.jp.
Kanako NakazawaDepartment of Forensic Psychiatry, National Center of Neurology and Psychiatry, National Institute of Mental Health, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8553, Japan. kanako@ncnp.go.jp.
Hideki TsumuraDepartment of Forensic Psychiatry, National Center of Neurology and Psychiatry, National Institute of Mental Health, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8553, Japan. tsumura@ncnp.go.jp.
Takayuki OkadaDepartment of Forensic Psychiatry, National Center of Neurology and Psychiatry, National Institute of Mental Health, 4-1-1, Ogawahigashi, Kodaira, Tokyo, 187-8553, Japan. takayukiok@ncnp.go.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSensori-perceptual processing of emotional stimuli under attentive conditions effectively prevents response disinhibition. This is observed saliently in low-impulsive people, because of their high sensitivity to warning signals, such as emotional faces. Results from human neurophysiological studies have been used to develop a dual detector model for early sensori-perceptual processing. A transient detector mechanism is related to automatic neurophysiological arousal in response to warning signals, which is reflected by early frontal event-related potential effects. The memory-based detector mechanism is associated with subsequent mismatch negativity (MMN), which reflects a short-term memory trace of signals. Based on previous findings, we predicted that impulsivity affects functional associations among the dual detector mechanisms, and modulates early frontal and/or MMN activities. In the present study, we recorded electroencephalograms for twenty-one healthy adults using a visual oddball paradigm with neutral faces as frequent stimuli, and angry and happy faces as infrequent stimuli. We measured the impulsivity traits by a self-report scale (the Barratt Impulsiveness Scale, 11th version).

resultsMain findings were that only happy faces increased early frontal negativity and subsequent occipital visual MMN (vMMN) for emotional change, and these neurophysiological effects positively correlated with each other in a temporally causal manner. However, an impulsivity sub-trait positively correlated selectively with vMMN for the happy faces.

conclusionThese findings demonstrate that higher impulsivity is associated with attenuated vMMN for emotional change detection in healthy populations, potentially because of weakened fronto-occipital functional connection that is responsible for the dual detector mechanism.

Indexed as

AdultBrainElectroencephalographyEmotionsEvoked PotentialsFacial ExpressionFacial RecognitionFemaleHumansImpulsive BehaviorMaleNeuropsychological TestsPersonalityPersonality TestsReaction TimeSelf Report

Identifiers

PMID26653995
PMCPMC4675059

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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.