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Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia

BACKGROUND: The “dysconnectivity hypothesis” was proposed 20 years ago. It characterized schizophrenia as a disorder with dysfunctional connectivity across a large range of distributed brain areas. Resting-state functional magnetic resonance imaging (rsfMRI) data have supported this theory. Previous...

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Autores principales: Yue, Jing-Li, Li, Peng, Shi, Le, Lin, Xiao, Sun, Hong-Qiang, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857898/
https://www.ncbi.nlm.nih.gov/pubmed/29560309
http://dx.doi.org/10.1016/j.nicl.2018.02.025
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author Yue, Jing-Li
Li, Peng
Shi, Le
Lin, Xiao
Sun, Hong-Qiang
Lu, Lin
author_facet Yue, Jing-Li
Li, Peng
Shi, Le
Lin, Xiao
Sun, Hong-Qiang
Lu, Lin
author_sort Yue, Jing-Li
collection PubMed
description BACKGROUND: The “dysconnectivity hypothesis” was proposed 20 years ago. It characterized schizophrenia as a disorder with dysfunctional connectivity across a large range of distributed brain areas. Resting-state functional magnetic resonance imaging (rsfMRI) data have supported this theory. Previous studies revealed that the amygdala might be responsible for the emotion regulation-related symptoms of schizophrenia. However, conventional methods oversimplified brain activities by assuming that it remained static throughout the entire scan duration, which may explain why inconsistent results have been reported for the same brain region. METHODS: An emerging technique is sliding time window analysis, which is used to describe functional connectivity based on the temporal variability of regions of interest (e.g., amygdala) in patients with schizophrenia. Conventional analysis of the static functional connectivity between the amygdala and whole brain was also conducted. RESULTS: Static functional connectivity between the amygdala and orbitofrontal region was impaired in patients with schizophrenia. The variability of connectivity between the amygdala and medial prefrontal cortex was enhanced (i.e., greater dynamics) in patients with schizophrenia. A negative relationship was found between the variability of connectivity and information processing efficiency. A positive correlation was found between the variability of connectivity and symptom severity. CONCLUSION: The findings suggest that schizophrenia was related to abnormal patterns of fluctuating communication among brain areas that are involved in emotion regulations. Unveiling the temporal properties of functional connectivity could disentangle the inconsistent results of previous functional connectivity studies.
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spelling pubmed-58578982018-03-20 Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia Yue, Jing-Li Li, Peng Shi, Le Lin, Xiao Sun, Hong-Qiang Lu, Lin Neuroimage Clin Regular Article BACKGROUND: The “dysconnectivity hypothesis” was proposed 20 years ago. It characterized schizophrenia as a disorder with dysfunctional connectivity across a large range of distributed brain areas. Resting-state functional magnetic resonance imaging (rsfMRI) data have supported this theory. Previous studies revealed that the amygdala might be responsible for the emotion regulation-related symptoms of schizophrenia. However, conventional methods oversimplified brain activities by assuming that it remained static throughout the entire scan duration, which may explain why inconsistent results have been reported for the same brain region. METHODS: An emerging technique is sliding time window analysis, which is used to describe functional connectivity based on the temporal variability of regions of interest (e.g., amygdala) in patients with schizophrenia. Conventional analysis of the static functional connectivity between the amygdala and whole brain was also conducted. RESULTS: Static functional connectivity between the amygdala and orbitofrontal region was impaired in patients with schizophrenia. The variability of connectivity between the amygdala and medial prefrontal cortex was enhanced (i.e., greater dynamics) in patients with schizophrenia. A negative relationship was found between the variability of connectivity and information processing efficiency. A positive correlation was found between the variability of connectivity and symptom severity. CONCLUSION: The findings suggest that schizophrenia was related to abnormal patterns of fluctuating communication among brain areas that are involved in emotion regulations. Unveiling the temporal properties of functional connectivity could disentangle the inconsistent results of previous functional connectivity studies. Elsevier 2018-02-27 /pmc/articles/PMC5857898/ /pubmed/29560309 http://dx.doi.org/10.1016/j.nicl.2018.02.025 Text en © 2018 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Yue, Jing-Li
Li, Peng
Shi, Le
Lin, Xiao
Sun, Hong-Qiang
Lu, Lin
Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title_full Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title_fullStr Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title_full_unstemmed Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title_short Enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
title_sort enhanced temporal variability of amygdala-frontal functional connectivity in patients with schizophrenia
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857898/
https://www.ncbi.nlm.nih.gov/pubmed/29560309
http://dx.doi.org/10.1016/j.nicl.2018.02.025
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