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Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients

Intra-individual variability (IIV) has received recent attention as an indicator of the stability of cognitive functioning that may outperform mean performance in reflecting putative neurobiological abnormalities. Increased IIV is regarded as a core deficit in schizophrenia patients; however, whethe...

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Autores principales: Shin, Ye Seul, Kim, Sung Nyun, Shin, Na Young, Jung, Wi Hoon, Hur, Ji-Won, Byun, Min Soo, Jang, Joon Hwan, An, Suk Kyoon, Kwon, Jun Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3832637/
https://www.ncbi.nlm.nih.gov/pubmed/24260112
http://dx.doi.org/10.1371/journal.pone.0078354
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author Shin, Ye Seul
Kim, Sung Nyun
Shin, Na Young
Jung, Wi Hoon
Hur, Ji-Won
Byun, Min Soo
Jang, Joon Hwan
An, Suk Kyoon
Kwon, Jun Soo
author_facet Shin, Ye Seul
Kim, Sung Nyun
Shin, Na Young
Jung, Wi Hoon
Hur, Ji-Won
Byun, Min Soo
Jang, Joon Hwan
An, Suk Kyoon
Kwon, Jun Soo
author_sort Shin, Ye Seul
collection PubMed
description Intra-individual variability (IIV) has received recent attention as an indicator of the stability of cognitive functioning that may outperform mean performance in reflecting putative neurobiological abnormalities. Increased IIV is regarded as a core deficit in schizophrenia patients; however, whether this deficit is present in the prodromal phase before the onset of schizophrenia has not been well established. In the present study, we investigated IIV using the stop-signal paradigm in at-risk mental state (ARMS) individuals and in schizophrenia patients. The study included 27 ARMS subjects, 37 schizophrenia patients, and 38 normal controls. The stop-signal task was administered to assess IIV and response inhibition. IIV was estimated by calculating the standard deviation across sub-blocks for the three groups. We observed increased IIV in ARMS subjects and schizophrenia patients compared with normal controls in both the “stop” and the “go” processes even though the mean response inhibition performances were not impaired in the ARMS group. Schizophrenia patients showed impaired response inhibition that was associated with the severity of negative symptoms. Our findings suggest that the analysis of IIV may identify cognitive and clinical features of ARMS that are not detectable by conventional mean performance analysis. The unstable response patterns associated with ARMS may originate from abnormal processing in neural systems caused by alterations in the integrity of functional brain networks and dopamine neuromodulation.
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spelling pubmed-38326372013-11-20 Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients Shin, Ye Seul Kim, Sung Nyun Shin, Na Young Jung, Wi Hoon Hur, Ji-Won Byun, Min Soo Jang, Joon Hwan An, Suk Kyoon Kwon, Jun Soo PLoS One Research Article Intra-individual variability (IIV) has received recent attention as an indicator of the stability of cognitive functioning that may outperform mean performance in reflecting putative neurobiological abnormalities. Increased IIV is regarded as a core deficit in schizophrenia patients; however, whether this deficit is present in the prodromal phase before the onset of schizophrenia has not been well established. In the present study, we investigated IIV using the stop-signal paradigm in at-risk mental state (ARMS) individuals and in schizophrenia patients. The study included 27 ARMS subjects, 37 schizophrenia patients, and 38 normal controls. The stop-signal task was administered to assess IIV and response inhibition. IIV was estimated by calculating the standard deviation across sub-blocks for the three groups. We observed increased IIV in ARMS subjects and schizophrenia patients compared with normal controls in both the “stop” and the “go” processes even though the mean response inhibition performances were not impaired in the ARMS group. Schizophrenia patients showed impaired response inhibition that was associated with the severity of negative symptoms. Our findings suggest that the analysis of IIV may identify cognitive and clinical features of ARMS that are not detectable by conventional mean performance analysis. The unstable response patterns associated with ARMS may originate from abnormal processing in neural systems caused by alterations in the integrity of functional brain networks and dopamine neuromodulation. Public Library of Science 2013-11-08 /pmc/articles/PMC3832637/ /pubmed/24260112 http://dx.doi.org/10.1371/journal.pone.0078354 Text en © 2013 Shin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shin, Ye Seul
Kim, Sung Nyun
Shin, Na Young
Jung, Wi Hoon
Hur, Ji-Won
Byun, Min Soo
Jang, Joon Hwan
An, Suk Kyoon
Kwon, Jun Soo
Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title_full Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title_fullStr Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title_full_unstemmed Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title_short Increased Intra-Individual Variability of Cognitive Processing in Subjects at Risk Mental State and Schizophrenia Patients
title_sort increased intra-individual variability of cognitive processing in subjects at risk mental state and schizophrenia patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3832637/
https://www.ncbi.nlm.nih.gov/pubmed/24260112
http://dx.doi.org/10.1371/journal.pone.0078354
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