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Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia
OBJECTIVE: Mismatch negativity (MMN) is known to be associated with neuro-cognition and functional outcomes. Remission and recovery rates are related to the neuro-cognition of patients with schizophrenia. The present study explored the relationship of MMN with remission in patients with schizophreni...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean College of Neuropsychopharmacology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006972/ https://www.ncbi.nlm.nih.gov/pubmed/31958913 http://dx.doi.org/10.9758/cpn.2020.18.1.127 |
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author | Kim, Ji Sun Kwon, Young Joon Lee, Hwa Young Lee, Ho-Sung Kim, Sungkean Shim, Se-hoon |
author_facet | Kim, Ji Sun Kwon, Young Joon Lee, Hwa Young Lee, Ho-Sung Kim, Sungkean Shim, Se-hoon |
author_sort | Kim, Ji Sun |
collection | PubMed |
description | OBJECTIVE: Mismatch negativity (MMN) is known to be associated with neuro-cognition and functional outcomes. Remission and recovery rates are related to the neuro-cognition of patients with schizophrenia. The present study explored the relationship of MMN with remission in patients with schizophrenia. METHODS: Forty patients with schizophrenia were recruited and divided into two groups, with or without remission, according to the Remission in Schizophrenia Working Group criteria (RSWGcr). Symptom severity (Positive and Negative Syndrome Scale, PANSS), cognitive function, functional outcome, and MMN of the patients were evaluated. A regression analysis was used to identify the factors that significantly predicted symptom improvement and remission including MMN at frontal site assessed at baseline, and anticipated clinical variables as predictive factors. RESULTS: MMN amplitudes in frontal sites were further decreased in the groups without remission compared to the groups with remission. MMN amplitude was significantly correlated with measures of symptom change and functional outcome measurements in patients with schizophrenia. Regression analysis revealed that symptom severity and MMN significantly predicted remission in patients with schizophrenia. Symptom improvement significantly predicted PANSS at baseline, illness duration, and antipsychotic dose, as did MMN amplitude at frontal site. CONCLUSION: Our results suggest that MMN reflected symptom improvement and remission in patients with schizophrenia. MMN indices appear to be promising candidates as predictive factors for schizophrenia remission. |
format | Online Article Text |
id | pubmed-7006972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean College of Neuropsychopharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70069722020-02-20 Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia Kim, Ji Sun Kwon, Young Joon Lee, Hwa Young Lee, Ho-Sung Kim, Sungkean Shim, Se-hoon Clin Psychopharmacol Neurosci Original Article OBJECTIVE: Mismatch negativity (MMN) is known to be associated with neuro-cognition and functional outcomes. Remission and recovery rates are related to the neuro-cognition of patients with schizophrenia. The present study explored the relationship of MMN with remission in patients with schizophrenia. METHODS: Forty patients with schizophrenia were recruited and divided into two groups, with or without remission, according to the Remission in Schizophrenia Working Group criteria (RSWGcr). Symptom severity (Positive and Negative Syndrome Scale, PANSS), cognitive function, functional outcome, and MMN of the patients were evaluated. A regression analysis was used to identify the factors that significantly predicted symptom improvement and remission including MMN at frontal site assessed at baseline, and anticipated clinical variables as predictive factors. RESULTS: MMN amplitudes in frontal sites were further decreased in the groups without remission compared to the groups with remission. MMN amplitude was significantly correlated with measures of symptom change and functional outcome measurements in patients with schizophrenia. Regression analysis revealed that symptom severity and MMN significantly predicted remission in patients with schizophrenia. Symptom improvement significantly predicted PANSS at baseline, illness duration, and antipsychotic dose, as did MMN amplitude at frontal site. CONCLUSION: Our results suggest that MMN reflected symptom improvement and remission in patients with schizophrenia. MMN indices appear to be promising candidates as predictive factors for schizophrenia remission. Korean College of Neuropsychopharmacology 2020-02 2020-02-29 /pmc/articles/PMC7006972/ /pubmed/31958913 http://dx.doi.org/10.9758/cpn.2020.18.1.127 Text en Copyright © 2020, Korean College of Neuropsychopharmacology This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Ji Sun Kwon, Young Joon Lee, Hwa Young Lee, Ho-Sung Kim, Sungkean Shim, Se-hoon Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title | Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title_full | Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title_fullStr | Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title_full_unstemmed | Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title_short | Mismatch Negativity Indices as a Prognostic Factor for Remission in Schizophrenia |
title_sort | mismatch negativity indices as a prognostic factor for remission in schizophrenia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006972/ https://www.ncbi.nlm.nih.gov/pubmed/31958913 http://dx.doi.org/10.9758/cpn.2020.18.1.127 |
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