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The neurophysiology of biological motion perception in schizophrenia

INTRODUCTION: The ability to recognize human biological motion is a fundamental aspect of social cognition that is impaired in people with schizophrenia. However, little is known about the neural substrates of impaired biological motion perception in schizophrenia. In the current study, we assessed...

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Autores principales: Jahshan, Carol, Wynn, Jonathan K, Mathis, Kristopher I, Green, Michael F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321396/
https://www.ncbi.nlm.nih.gov/pubmed/25722951
http://dx.doi.org/10.1002/brb3.303
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author Jahshan, Carol
Wynn, Jonathan K
Mathis, Kristopher I
Green, Michael F
author_facet Jahshan, Carol
Wynn, Jonathan K
Mathis, Kristopher I
Green, Michael F
author_sort Jahshan, Carol
collection PubMed
description INTRODUCTION: The ability to recognize human biological motion is a fundamental aspect of social cognition that is impaired in people with schizophrenia. However, little is known about the neural substrates of impaired biological motion perception in schizophrenia. In the current study, we assessed event-related potentials (ERPs) to human and nonhuman movement in schizophrenia. METHODS: Twenty-four subjects with schizophrenia and 18 healthy controls completed a biological motion task while their electroencephalography (EEG) was simultaneously recorded. Subjects watched clips of point-light animations containing 100%, 85%, or 70% biological motion, and were asked to decide whether the clip resembled human or nonhuman movement. Three ERPs were examined: P1, N1, and the late positive potential (LPP). RESULTS: Behaviorally, schizophrenia subjects identified significantly fewer stimuli as human movement compared to healthy controls in the 100% and 85% conditions. At the neural level, P1 was reduced in the schizophrenia group but did not differ among conditions in either group. There were no group differences in N1 but both groups had the largest N1 in the 70% condition. There was a condition × group interaction for the LPP: Healthy controls had a larger LPP to 100% versus 85% and 70% biological motion; there was no difference among conditions in schizophrenia subjects. CONCLUSIONS: Consistent with previous findings, schizophrenia subjects were impaired in their ability to recognize biological motion. The EEG results showed that biological motion did not influence the earliest stage of visual processing (P1). Although schizophrenia subjects showed the same pattern of N1 results relative to healthy controls, they were impaired at a later stage (LPP), reflecting a dysfunction in the identification of human form in biological versus nonbiological motion stimuli.
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spelling pubmed-43213962015-02-26 The neurophysiology of biological motion perception in schizophrenia Jahshan, Carol Wynn, Jonathan K Mathis, Kristopher I Green, Michael F Brain Behav Original Research INTRODUCTION: The ability to recognize human biological motion is a fundamental aspect of social cognition that is impaired in people with schizophrenia. However, little is known about the neural substrates of impaired biological motion perception in schizophrenia. In the current study, we assessed event-related potentials (ERPs) to human and nonhuman movement in schizophrenia. METHODS: Twenty-four subjects with schizophrenia and 18 healthy controls completed a biological motion task while their electroencephalography (EEG) was simultaneously recorded. Subjects watched clips of point-light animations containing 100%, 85%, or 70% biological motion, and were asked to decide whether the clip resembled human or nonhuman movement. Three ERPs were examined: P1, N1, and the late positive potential (LPP). RESULTS: Behaviorally, schizophrenia subjects identified significantly fewer stimuli as human movement compared to healthy controls in the 100% and 85% conditions. At the neural level, P1 was reduced in the schizophrenia group but did not differ among conditions in either group. There were no group differences in N1 but both groups had the largest N1 in the 70% condition. There was a condition × group interaction for the LPP: Healthy controls had a larger LPP to 100% versus 85% and 70% biological motion; there was no difference among conditions in schizophrenia subjects. CONCLUSIONS: Consistent with previous findings, schizophrenia subjects were impaired in their ability to recognize biological motion. The EEG results showed that biological motion did not influence the earliest stage of visual processing (P1). Although schizophrenia subjects showed the same pattern of N1 results relative to healthy controls, they were impaired at a later stage (LPP), reflecting a dysfunction in the identification of human form in biological versus nonbiological motion stimuli. BlackWell Publishing Ltd 2015-01 2014-12-18 /pmc/articles/PMC4321396/ /pubmed/25722951 http://dx.doi.org/10.1002/brb3.303 Text en © 2014 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Jahshan, Carol
Wynn, Jonathan K
Mathis, Kristopher I
Green, Michael F
The neurophysiology of biological motion perception in schizophrenia
title The neurophysiology of biological motion perception in schizophrenia
title_full The neurophysiology of biological motion perception in schizophrenia
title_fullStr The neurophysiology of biological motion perception in schizophrenia
title_full_unstemmed The neurophysiology of biological motion perception in schizophrenia
title_short The neurophysiology of biological motion perception in schizophrenia
title_sort neurophysiology of biological motion perception in schizophrenia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321396/
https://www.ncbi.nlm.nih.gov/pubmed/25722951
http://dx.doi.org/10.1002/brb3.303
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