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Disrupted modular organization of primary sensory brain areas in schizophrenia
Abnormal brain resting-state functional connectivity has been consistently observed in patients affected by schizophrenia (SCZ) using functional MRI and other neuroimaging techniques. Graph theoretical methods provide a framework to investigate these defective functional interactions and their effec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987872/ https://www.ncbi.nlm.nih.gov/pubmed/29876260 http://dx.doi.org/10.1016/j.nicl.2018.02.035 |
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author | Bordier, Cécile Nicolini, Carlo Forcellini, Giulia Bifone, Angelo |
author_facet | Bordier, Cécile Nicolini, Carlo Forcellini, Giulia Bifone, Angelo |
author_sort | Bordier, Cécile |
collection | PubMed |
description | Abnormal brain resting-state functional connectivity has been consistently observed in patients affected by schizophrenia (SCZ) using functional MRI and other neuroimaging techniques. Graph theoretical methods provide a framework to investigate these defective functional interactions and their effects on the organization of brain connectivity networks. A few studies have shown altered distribution of connectivity within and between functional modules in SCZ patients, an indication of imbalanced functional segregation ad integration. However, no major alterations of modular organization have been reported in patients, and unambiguous identification of the neural substrates affected remains elusive. Recently, it has been demonstrated that current modularity analysis methods suffer from a fundamental and severe resolution limit, as they fail to detect features that are smaller than a scale determined by the size of the entire connectivity network. This resolution limit is likely to have hampered the ability to resolve differences between patients and controls in previous studies. Here, we apply Surprise, a novel resolution limit-free approach, to study the modular organization of resting state functional connectivity networks in a large cohort of SCZ patients and in matched healthy controls. Leveraging these important methodological advances we find new evidence of substantial fragmentation and reorganization involving primary sensory, auditory and visual areas in SCZ patients. Conversely, frontal and prefrontal areas, typically associated with higher cognitive functions, appear to be largely unaffected, with changes selectively involving language and speech processing areas. Our findings support the hypothesis that cognitive dysfunction in SCZ may involve deficits occurring already at early stages of sensory processing. |
format | Online Article Text |
id | pubmed-5987872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-59878722018-06-06 Disrupted modular organization of primary sensory brain areas in schizophrenia Bordier, Cécile Nicolini, Carlo Forcellini, Giulia Bifone, Angelo Neuroimage Clin Regular Article Abnormal brain resting-state functional connectivity has been consistently observed in patients affected by schizophrenia (SCZ) using functional MRI and other neuroimaging techniques. Graph theoretical methods provide a framework to investigate these defective functional interactions and their effects on the organization of brain connectivity networks. A few studies have shown altered distribution of connectivity within and between functional modules in SCZ patients, an indication of imbalanced functional segregation ad integration. However, no major alterations of modular organization have been reported in patients, and unambiguous identification of the neural substrates affected remains elusive. Recently, it has been demonstrated that current modularity analysis methods suffer from a fundamental and severe resolution limit, as they fail to detect features that are smaller than a scale determined by the size of the entire connectivity network. This resolution limit is likely to have hampered the ability to resolve differences between patients and controls in previous studies. Here, we apply Surprise, a novel resolution limit-free approach, to study the modular organization of resting state functional connectivity networks in a large cohort of SCZ patients and in matched healthy controls. Leveraging these important methodological advances we find new evidence of substantial fragmentation and reorganization involving primary sensory, auditory and visual areas in SCZ patients. Conversely, frontal and prefrontal areas, typically associated with higher cognitive functions, appear to be largely unaffected, with changes selectively involving language and speech processing areas. Our findings support the hypothesis that cognitive dysfunction in SCZ may involve deficits occurring already at early stages of sensory processing. Elsevier 2018-03-01 /pmc/articles/PMC5987872/ /pubmed/29876260 http://dx.doi.org/10.1016/j.nicl.2018.02.035 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article Bordier, Cécile Nicolini, Carlo Forcellini, Giulia Bifone, Angelo Disrupted modular organization of primary sensory brain areas in schizophrenia |
title | Disrupted modular organization of primary sensory brain areas in schizophrenia |
title_full | Disrupted modular organization of primary sensory brain areas in schizophrenia |
title_fullStr | Disrupted modular organization of primary sensory brain areas in schizophrenia |
title_full_unstemmed | Disrupted modular organization of primary sensory brain areas in schizophrenia |
title_short | Disrupted modular organization of primary sensory brain areas in schizophrenia |
title_sort | disrupted modular organization of primary sensory brain areas in schizophrenia |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987872/ https://www.ncbi.nlm.nih.gov/pubmed/29876260 http://dx.doi.org/10.1016/j.nicl.2018.02.035 |
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