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Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia
BACKGROUND: The functional architecture of resting-state networks (RSNs) is defined by their connectivity and metastability. Disrupted RSN connectivity has been amply demonstrated in schizophrenia while the role of metastability remains poorly defined. Here, we undertake a comprehensive characterisa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317903/ https://www.ncbi.nlm.nih.gov/pubmed/29709491 http://dx.doi.org/10.1016/j.schres.2018.04.029 |
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author | Lee, Won Hee Doucet, Gaelle E. Leibu, Evan Frangou, Sophia |
author_facet | Lee, Won Hee Doucet, Gaelle E. Leibu, Evan Frangou, Sophia |
author_sort | Lee, Won Hee |
collection | PubMed |
description | BACKGROUND: The functional architecture of resting-state networks (RSNs) is defined by their connectivity and metastability. Disrupted RSN connectivity has been amply demonstrated in schizophrenia while the role of metastability remains poorly defined. Here, we undertake a comprehensive characterisation of RSN organization in schizophrenia and test its contribution to the clinical profile of this disorder. METHODS: We extracted RSNs representing the default mode (DMN), central executive (CEN), salience (SAL), language (LAN), sensorimotor (SMN), auditory (AN) and visual (VN) networks from resting-state functional magnetic resonance imaging data obtained from patients with schizophrenia (n = 85) and healthy individuals (n = 48). For each network, we computed its functional cohesiveness and integration and used the Kuramoto order parameter to compute metastability. We used stepwise multiple regression analyses to test these RSN features as predictors of symptom severity in patients. RESULTS: RSN features respectively explained 14%, 17%, 12% and 5% of the variance in positive, negative, anxious/ depressive and agitation/disorganization symptoms. Lower functional integration between the DMN, CEN and SMN primarily contributed to positive symptoms. The functional properties of the SAL network were key predictors of all other symptom dimensions; specifically, lower cohesiveness of the SAL, lower integration of this network with the LAN and higher integration with the CEN respectively contributed to negative, anxious/depressive and disorganization symptoms. Increased SAL metastability was associated with negative symptoms. CONCLUSIONS: These results confirm the primacy of the SAL network for schizophrenia and demonstrate that abnormalities in RSN connectivity and metastability are significant predictors of schizophrenia-related psychopathology. |
format | Online Article Text |
id | pubmed-6317903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-63179032019-01-03 Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia Lee, Won Hee Doucet, Gaelle E. Leibu, Evan Frangou, Sophia Schizophr Res Article BACKGROUND: The functional architecture of resting-state networks (RSNs) is defined by their connectivity and metastability. Disrupted RSN connectivity has been amply demonstrated in schizophrenia while the role of metastability remains poorly defined. Here, we undertake a comprehensive characterisation of RSN organization in schizophrenia and test its contribution to the clinical profile of this disorder. METHODS: We extracted RSNs representing the default mode (DMN), central executive (CEN), salience (SAL), language (LAN), sensorimotor (SMN), auditory (AN) and visual (VN) networks from resting-state functional magnetic resonance imaging data obtained from patients with schizophrenia (n = 85) and healthy individuals (n = 48). For each network, we computed its functional cohesiveness and integration and used the Kuramoto order parameter to compute metastability. We used stepwise multiple regression analyses to test these RSN features as predictors of symptom severity in patients. RESULTS: RSN features respectively explained 14%, 17%, 12% and 5% of the variance in positive, negative, anxious/ depressive and agitation/disorganization symptoms. Lower functional integration between the DMN, CEN and SMN primarily contributed to positive symptoms. The functional properties of the SAL network were key predictors of all other symptom dimensions; specifically, lower cohesiveness of the SAL, lower integration of this network with the LAN and higher integration with the CEN respectively contributed to negative, anxious/depressive and disorganization symptoms. Increased SAL metastability was associated with negative symptoms. CONCLUSIONS: These results confirm the primacy of the SAL network for schizophrenia and demonstrate that abnormalities in RSN connectivity and metastability are significant predictors of schizophrenia-related psychopathology. 2018-04-27 2018-11 /pmc/articles/PMC6317903/ /pubmed/29709491 http://dx.doi.org/10.1016/j.schres.2018.04.029 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lee, Won Hee Doucet, Gaelle E. Leibu, Evan Frangou, Sophia Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title | Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title_full | Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title_fullStr | Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title_full_unstemmed | Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title_short | Resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
title_sort | resting-state network connectivity and metastability predict clinical symptoms in schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317903/ https://www.ncbi.nlm.nih.gov/pubmed/29709491 http://dx.doi.org/10.1016/j.schres.2018.04.029 |
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