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Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia

The notion of dysconnectivity in schizophrenia has been put forward for many years and results in substantial attempts to explore altered functional connectivity (FC) within different networks with inconsistent results. Clinical, demographical, and methodological heterogeneity may contribute to the...

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Autores principales: Ding, Yudan, Ou, Yangpan, Su, Qinji, Pan, Pan, Shan, Xiaoxiao, Chen, Jindong, Liu, Feng, Zhang, Zhikun, Zhao, Jingping, Guo, Wenbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399149/
https://www.ncbi.nlm.nih.gov/pubmed/30863277
http://dx.doi.org/10.3389/fnins.2019.00145
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author Ding, Yudan
Ou, Yangpan
Su, Qinji
Pan, Pan
Shan, Xiaoxiao
Chen, Jindong
Liu, Feng
Zhang, Zhikun
Zhao, Jingping
Guo, Wenbin
author_facet Ding, Yudan
Ou, Yangpan
Su, Qinji
Pan, Pan
Shan, Xiaoxiao
Chen, Jindong
Liu, Feng
Zhang, Zhikun
Zhao, Jingping
Guo, Wenbin
author_sort Ding, Yudan
collection PubMed
description The notion of dysconnectivity in schizophrenia has been put forward for many years and results in substantial attempts to explore altered functional connectivity (FC) within different networks with inconsistent results. Clinical, demographical, and methodological heterogeneity may contribute to the inconsistency. Forty-four patients with first-episode, drug-naive schizophrenia, 42 unaffected siblings of schizophrenia patients and 44 healthy controls took part in this study. Global-brain FC (GFC) was employed to analyze the imaging data. Compared with healthy controls, patients with schizophrenia and unaffected siblings shared enhanced GFC in the left superior frontal gyrus (SFG). In addition, patients had increased GFC mainly in the thalamo-cortical network, including the bilateral thalamus, bilateral posterior cingulate cortex (PCC)/precuneus, left superior medial prefrontal cortex (MPFC), right angular gyrus, and right SFG/middle frontal gyrus and decreased GFC in the left ITG/cerebellum Crus I. No other altered GFC values were observed in the siblings group relative to the control group. Further ROC analysis showed that increased GFC in the left SFG could separate the patients or the siblings from the controls with acceptable sensitivities. Our findings suggest that increased GFC in the left SFG may serve as a potential endophenotype for schizophrenia.
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spelling pubmed-63991492019-03-12 Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia Ding, Yudan Ou, Yangpan Su, Qinji Pan, Pan Shan, Xiaoxiao Chen, Jindong Liu, Feng Zhang, Zhikun Zhao, Jingping Guo, Wenbin Front Neurosci Neuroscience The notion of dysconnectivity in schizophrenia has been put forward for many years and results in substantial attempts to explore altered functional connectivity (FC) within different networks with inconsistent results. Clinical, demographical, and methodological heterogeneity may contribute to the inconsistency. Forty-four patients with first-episode, drug-naive schizophrenia, 42 unaffected siblings of schizophrenia patients and 44 healthy controls took part in this study. Global-brain FC (GFC) was employed to analyze the imaging data. Compared with healthy controls, patients with schizophrenia and unaffected siblings shared enhanced GFC in the left superior frontal gyrus (SFG). In addition, patients had increased GFC mainly in the thalamo-cortical network, including the bilateral thalamus, bilateral posterior cingulate cortex (PCC)/precuneus, left superior medial prefrontal cortex (MPFC), right angular gyrus, and right SFG/middle frontal gyrus and decreased GFC in the left ITG/cerebellum Crus I. No other altered GFC values were observed in the siblings group relative to the control group. Further ROC analysis showed that increased GFC in the left SFG could separate the patients or the siblings from the controls with acceptable sensitivities. Our findings suggest that increased GFC in the left SFG may serve as a potential endophenotype for schizophrenia. Frontiers Media S.A. 2019-02-26 /pmc/articles/PMC6399149/ /pubmed/30863277 http://dx.doi.org/10.3389/fnins.2019.00145 Text en Copyright © 2019 Ding, Ou, Su, Pan, Shan, Chen, Liu, Zhang, Zhao and Guo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Ding, Yudan
Ou, Yangpan
Su, Qinji
Pan, Pan
Shan, Xiaoxiao
Chen, Jindong
Liu, Feng
Zhang, Zhikun
Zhao, Jingping
Guo, Wenbin
Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title_full Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title_fullStr Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title_full_unstemmed Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title_short Enhanced Global-Brain Functional Connectivity in the Left Superior Frontal Gyrus as a Possible Endophenotype for Schizophrenia
title_sort enhanced global-brain functional connectivity in the left superior frontal gyrus as a possible endophenotype for schizophrenia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399149/
https://www.ncbi.nlm.nih.gov/pubmed/30863277
http://dx.doi.org/10.3389/fnins.2019.00145
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