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Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively

Like socio-economic status and cognitive abilities, personality traits predict important life outcomes. Traits that reflect unusually low or high approach motivations, such as low extraversion and high disinhibition, are linked to various forms of mental disorder. Similarly, the dopamine system is t...

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Autores principales: Neo, Phoebe S-H., McNaughton, Neil, Sellbom, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645529/
https://www.ncbi.nlm.nih.gov/pubmed/34909564
http://dx.doi.org/10.1017/pen.2021.4
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author Neo, Phoebe S-H.
McNaughton, Neil
Sellbom, Martin
author_facet Neo, Phoebe S-H.
McNaughton, Neil
Sellbom, Martin
author_sort Neo, Phoebe S-H.
collection PubMed
description Like socio-economic status and cognitive abilities, personality traits predict important life outcomes. Traits that reflect unusually low or high approach motivations, such as low extraversion and high disinhibition, are linked to various forms of mental disorder. Similarly, the dopamine system is theoretically linked to approach motivation traits and to various forms of mental disorder. Identifying neural contributions to extremes of such traits should map to neural sources of psychopathology, with dopamine a prime candidate. Notably, dopamine cells fire in response to unexpected reward, which suggests that the size of non-invasive, scalp-recorded potentials evoked by unexpected reward could reflect sensitivity in approach motivation traits. Here, we evaluated the validity of evoked electroencephalography (EEG) responses to unexpected reward in a monetary gain/loss task to assess approach motivation traits in 137 participants, oversampled for externalizing psychopathology symptoms. We demonstrated that over the 0–400 ms period in which feedback on the outcome was presented, responses evoked by unexpected reward contributed to all theoretically relevant approach motivation trait domains (disinhibition, extraversion and the behavioural activation system); and did so only at times when dopamine responses normally peak and reportedly code salience (70–100 ms) and valuation (200–300 ms). In particular, we linked “dopaminergic” salience and valuation to the psychopathology-related constructs of low extraversion (social anxiety) and high disinhibition (impulsivity) respectively, making the evoked potential components biomarker candidates for indexing aberrant processing of unexpected reward.
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spelling pubmed-86455292021-12-13 Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively Neo, Phoebe S-H. McNaughton, Neil Sellbom, Martin Personal Neurosci Empirical Paper Like socio-economic status and cognitive abilities, personality traits predict important life outcomes. Traits that reflect unusually low or high approach motivations, such as low extraversion and high disinhibition, are linked to various forms of mental disorder. Similarly, the dopamine system is theoretically linked to approach motivation traits and to various forms of mental disorder. Identifying neural contributions to extremes of such traits should map to neural sources of psychopathology, with dopamine a prime candidate. Notably, dopamine cells fire in response to unexpected reward, which suggests that the size of non-invasive, scalp-recorded potentials evoked by unexpected reward could reflect sensitivity in approach motivation traits. Here, we evaluated the validity of evoked electroencephalography (EEG) responses to unexpected reward in a monetary gain/loss task to assess approach motivation traits in 137 participants, oversampled for externalizing psychopathology symptoms. We demonstrated that over the 0–400 ms period in which feedback on the outcome was presented, responses evoked by unexpected reward contributed to all theoretically relevant approach motivation trait domains (disinhibition, extraversion and the behavioural activation system); and did so only at times when dopamine responses normally peak and reportedly code salience (70–100 ms) and valuation (200–300 ms). In particular, we linked “dopaminergic” salience and valuation to the psychopathology-related constructs of low extraversion (social anxiety) and high disinhibition (impulsivity) respectively, making the evoked potential components biomarker candidates for indexing aberrant processing of unexpected reward. Cambridge University Press 2021-11-12 /pmc/articles/PMC8645529/ /pubmed/34909564 http://dx.doi.org/10.1017/pen.2021.4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Empirical Paper
Neo, Phoebe S-H.
McNaughton, Neil
Sellbom, Martin
Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title_full Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title_fullStr Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title_full_unstemmed Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title_short Early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
title_sort early and late signals of unexpected reward contribute to low extraversion and high disinhibition, respectively
topic Empirical Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645529/
https://www.ncbi.nlm.nih.gov/pubmed/34909564
http://dx.doi.org/10.1017/pen.2021.4
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