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Neurophysiological Correlates of Configural Face Processing in Schizotypy

Background: Face processing impairment in schizophrenia appears to be underpinned by poor configural (as opposed to feature-based) processing; however, few studies have sought to characterize this impairment electrophysiologically. Given the sensitivity of event-related potentials to antipsychotic m...

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Autores principales: Batty, Rachel A., Francis, Andrew J. P., Innes-Brown, Hamish, Joshua, Nicole R., Rossell, Susan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129627/
https://www.ncbi.nlm.nih.gov/pubmed/25161628
http://dx.doi.org/10.3389/fpsyt.2014.00101
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author Batty, Rachel A.
Francis, Andrew J. P.
Innes-Brown, Hamish
Joshua, Nicole R.
Rossell, Susan L.
author_facet Batty, Rachel A.
Francis, Andrew J. P.
Innes-Brown, Hamish
Joshua, Nicole R.
Rossell, Susan L.
author_sort Batty, Rachel A.
collection PubMed
description Background: Face processing impairment in schizophrenia appears to be underpinned by poor configural (as opposed to feature-based) processing; however, few studies have sought to characterize this impairment electrophysiologically. Given the sensitivity of event-related potentials to antipsychotic medications, and the potential for neurophysiological abnormalities to serve as vulnerability markers for schizophrenia, a handful of studies have investigated early visual P100 and face-selective N170 in “at risk” populations. However, this is the first known neurophysiological investigation of configural face processing in a non-clinical schizotypal sample. Methods: Using stimuli designed to engage configural processing in face perception (upright and inverted Mooney and photographic faces), P100 and N170 components were recorded in healthy individuals characterized by high (N = 14) and low (N = 14) schizotypal traits according to the Oxford–Liverpool Inventory of Feelings and Experiences. Results: High schizotypes showed significantly reduced N170 amplitudes to inverted photographic faces. Typical N170 latency and amplitude inversion effects (delayed and enhanced N170 to inverted relative to upright photographic faces, and enhanced amplitude to upright versus inverted Mooney faces), were demonstrated by low, but not high, schizotypes. No group differences were shown for P100 analyses. Conclusions: The findings suggest that neurophysiological deficits in processing facial configurations (N170) are apparent in schizotypy, while the early sensory processing (P100) of faces appears intact. This work adds to the mounting evidence for analogous neural processing anomalies at the healthy end of the psychosis continuum.
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spelling pubmed-41296272014-08-26 Neurophysiological Correlates of Configural Face Processing in Schizotypy Batty, Rachel A. Francis, Andrew J. P. Innes-Brown, Hamish Joshua, Nicole R. Rossell, Susan L. Front Psychiatry Psychiatry Background: Face processing impairment in schizophrenia appears to be underpinned by poor configural (as opposed to feature-based) processing; however, few studies have sought to characterize this impairment electrophysiologically. Given the sensitivity of event-related potentials to antipsychotic medications, and the potential for neurophysiological abnormalities to serve as vulnerability markers for schizophrenia, a handful of studies have investigated early visual P100 and face-selective N170 in “at risk” populations. However, this is the first known neurophysiological investigation of configural face processing in a non-clinical schizotypal sample. Methods: Using stimuli designed to engage configural processing in face perception (upright and inverted Mooney and photographic faces), P100 and N170 components were recorded in healthy individuals characterized by high (N = 14) and low (N = 14) schizotypal traits according to the Oxford–Liverpool Inventory of Feelings and Experiences. Results: High schizotypes showed significantly reduced N170 amplitudes to inverted photographic faces. Typical N170 latency and amplitude inversion effects (delayed and enhanced N170 to inverted relative to upright photographic faces, and enhanced amplitude to upright versus inverted Mooney faces), were demonstrated by low, but not high, schizotypes. No group differences were shown for P100 analyses. Conclusions: The findings suggest that neurophysiological deficits in processing facial configurations (N170) are apparent in schizotypy, while the early sensory processing (P100) of faces appears intact. This work adds to the mounting evidence for analogous neural processing anomalies at the healthy end of the psychosis continuum. Frontiers Media S.A. 2014-08-12 /pmc/articles/PMC4129627/ /pubmed/25161628 http://dx.doi.org/10.3389/fpsyt.2014.00101 Text en Copyright © 2014 Batty, Francis, Innes-Brown, Joshua and Rossell. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Batty, Rachel A.
Francis, Andrew J. P.
Innes-Brown, Hamish
Joshua, Nicole R.
Rossell, Susan L.
Neurophysiological Correlates of Configural Face Processing in Schizotypy
title Neurophysiological Correlates of Configural Face Processing in Schizotypy
title_full Neurophysiological Correlates of Configural Face Processing in Schizotypy
title_fullStr Neurophysiological Correlates of Configural Face Processing in Schizotypy
title_full_unstemmed Neurophysiological Correlates of Configural Face Processing in Schizotypy
title_short Neurophysiological Correlates of Configural Face Processing in Schizotypy
title_sort neurophysiological correlates of configural face processing in schizotypy
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129627/
https://www.ncbi.nlm.nih.gov/pubmed/25161628
http://dx.doi.org/10.3389/fpsyt.2014.00101
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