Cited by 181Functional Brain Connectivity StudiesSchizophrenia research and treatmentMental Health and Psychiatry

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Disruption of Anterior Insula Modulation of Large-Scale Brain Networks in Schizophrenia

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Moran, Lauren V., Tagamets, Malle A., Sampath, Hemalatha, O’Donnell, Alan, Stein, Elliot A., Kochunov, Peter, Hong, L. Elliot·2013·Biological Psychiatry

DOI 10.1016/j.biopsych.2013.02.029PMC PMC3735654

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Abstract

Background Systems level modeling of functional magnetic resonance imaging data has demonstrated dysfunction of several large-scale brain networks in schizophrenia. Anomalies across multiple functional networks associated with schizophrenia could be due to diffuse pathology across multiple networks or, alternatively, dysfunction at converging control(s) common to these networks. The right anterior insula has been shown to modulate activity in the central executive and default mode networks in healthy individuals. We tested the hypothesis that right anterior insula modulation of central executive and default mode networks is disrupted in schizophrenia and associated with cognitive deficits.Methods In 44 patients with schizophrenia and 44 healthy control subjects, we used seed-based resting state functional connectivity functional magnetic resonance imaging analysis to examine connectivity between right insular subregions and central executive/default mode network regions. We also performed two directed connectivity analyses of resting state data: Granger analysis and confirmatory structural equation modeling. Between-group differences in path coefficients were used to evaluate anterior insula modulation of central executive and default mode networks. Cognitive performance was assessed with the rapid visual information processing task, a test of sustained attention.Results With multiple connectivity techniques, we found compelling, corroborative evidence of disruption of right anterior insula modulation of central executive and default mode networks in patients with schizophrenia. The strength of right anterior insula modulation of these networks predicted cognitive performance.Conclusions Individuals with schizophrenia have impaired right anterior insula modulation of large-scale brain networks. The right anterior insula might be an emergent pathophysiological gateway in schizophrenia.

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A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190
The Brief Psychiatric Rating Scale.
Overall, J. E., & Gorham, D. R. (1962) · Psychological Reports · doi:10.2466/pr0.1962.10.3.799 · Cited by 11,090
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · cited 1×
“AIns modulation of large-scale networks is lateralized and specific to the right AIns, possibly related to its role in interoceptive awareness of physically and emotionally arousing stimuli such as pain (22, 23), or to right-hemisphere lateralization of sympathetic nervous system control (24).”
Background
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592
Large-scale brain networks and psychopathology: a unifying triple network model
Menon, V. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.08.003 · Cited by 4,168
A critical role for the right fronto-insular cortex in switching between central-executive and default-mode networks
Sridharan, D., Levitin, D. J., & Menon, V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800005105 · Cited by 2,892

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Smallwood, R. F., Hutson, R., & Robin, D. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-386456-7.05217-5 · Cited by 6
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Zhang, L., Shi, L., Zhang, B., Zhao, L., Dong, Y., Liu, J., Lian, Z., Liang, L., Chen, W., Luo, X., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178386 · Cited by 5
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Bos, D. J., Ajodan, E. L., Silverman, M. R., Dyke, J. P., Durston, S., Power, J. D., & Jones, R. M. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx127 · Cited by 4
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Authors: Moran, L. V., Tagamets, M. A., Sampath, H., O’Donnell, A., Stein, E. A., Kochunov, P., & Hong, L. E.
Affiliations: University of Maryland, Baltimore (US)
National Institutes of Health (US)
Corresponding author: Moran, Lauren V.
ORCID: Moran, Lauren V.
Sampath, Hemalatha
Stein, Elliot A.
Kochunov, Peter
Hong, L. Elliot
Venue: Biological Psychiatry
Publisher: Elsevier BV
Published: 2013-09
Volume: 74
Issue: 6
Pages: 467-474
ISSN: 0006-3223 (ISSN-L)
DOI: 10.1016/j.biopsych.2013.02.029
PMC: PMC3735654
OpenAlex: W2015335162
Cited by: 181
References: 61
Citations by year: 2026: 3 · 2025: 6 · 2024: 13 · 2023: 11 · 2022: 17 · 2021: 11 · 2020: 14 · 2019: 16 · 2018: 20 · 2017: 21 · 2016: 15 · 2015: 20 · 2014: 10 · 2013: 4
FWCI: 8.92
Type: journal article
Language: en
Open access: green
europepmc.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Biological Psychiatry (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute on Drug Abuse
National Institutes of Health (R21DA033817, T32MH067533, R01MH085646, R01DA027680)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Social Sciences › Arts and Humanities › Philosophy › Mental Health and Psychiatry
Keywords: schizophrenia, right anterior insula, large-scale brain networks, frontoparietal network, default mode network, resting-state functional connectivity, directed connectivity, Granger causality, cognitive impairment, sustained attention, rapid visual information processing
MeSH terms: Adult, Cerebral Cortex, Female, Humans, Magnetic Resonance Imaging, Male, Nerve Net, Schizophrenia

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Disruption of Anterior Insula Modulation of Large-Scale Brain Networks in Schizophrenia

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