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Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder

Convergent evidence supports regional dysfunction within a corticolimbic neural system that subserves emotional processing and regulation in adolescents and adults with bipolar disorder (BD), with abnormalities prominent within the amygdala and its major anterior paralimbic cortical connection sites...

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Autores principales: Wang, Fei, Bobrow, Laurel, Liu, Jie, Spencer, Linda, Blumberg, Hilary P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503984/
https://www.ncbi.nlm.nih.gov/pubmed/23185566
http://dx.doi.org/10.1371/journal.pone.0050177
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author Wang, Fei
Bobrow, Laurel
Liu, Jie
Spencer, Linda
Blumberg, Hilary P.
author_facet Wang, Fei
Bobrow, Laurel
Liu, Jie
Spencer, Linda
Blumberg, Hilary P.
author_sort Wang, Fei
collection PubMed
description Convergent evidence supports regional dysfunction within a corticolimbic neural system that subserves emotional processing and regulation in adolescents and adults with bipolar disorder (BD), with abnormalities prominent within the amygdala and its major anterior paralimbic cortical connection sites including ventral anterior cingulate, orbitofrontal, insular and temporopolar cortices. Recent studies of adults with BD demonstrate abnormalities in the functional connectivity between the amygdala and anterior paralimbic regions suggesting an important role for the connections between these regions in the development of the disorder. This study tests the hypothesis that these functional connectivity abnormalities are present in adolescents with BD. Fifty-seven adolescents, twenty-one with BD and thirty-six healthy comparison (HC) adolescents, participated in functional magnetic resonance imaging while processing emotional face stimuli. The BD and HC groups were compared in the strength of functional connectivity from amygdala to the anterior paralimbic cortical regions, and explored in remaining brain regions. Functional connectivity was decreased in the BD group, compared to the HC group, during processing of emotional faces in ventral anterior cingulate (VACC), orbitofrontal, insular and temporopolar cortices (p<0.005). Orbitofrontal and VACC findings for the happy condition, and additionally right insula for the neutral condition, survived multiple comparison correction. Exploratory analyses did not reveal additional regions of group differences. This study provides evidence for decreased functional connectivity between the amygdala and anterior paralimbic cortices in adolescents with BD. This suggests that amygdala-anterior paralimbic connectivity abnormalities are early features of BD that emerge at least by adolescence in the disorder.
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spelling pubmed-35039842012-11-26 Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder Wang, Fei Bobrow, Laurel Liu, Jie Spencer, Linda Blumberg, Hilary P. PLoS One Research Article Convergent evidence supports regional dysfunction within a corticolimbic neural system that subserves emotional processing and regulation in adolescents and adults with bipolar disorder (BD), with abnormalities prominent within the amygdala and its major anterior paralimbic cortical connection sites including ventral anterior cingulate, orbitofrontal, insular and temporopolar cortices. Recent studies of adults with BD demonstrate abnormalities in the functional connectivity between the amygdala and anterior paralimbic regions suggesting an important role for the connections between these regions in the development of the disorder. This study tests the hypothesis that these functional connectivity abnormalities are present in adolescents with BD. Fifty-seven adolescents, twenty-one with BD and thirty-six healthy comparison (HC) adolescents, participated in functional magnetic resonance imaging while processing emotional face stimuli. The BD and HC groups were compared in the strength of functional connectivity from amygdala to the anterior paralimbic cortical regions, and explored in remaining brain regions. Functional connectivity was decreased in the BD group, compared to the HC group, during processing of emotional faces in ventral anterior cingulate (VACC), orbitofrontal, insular and temporopolar cortices (p<0.005). Orbitofrontal and VACC findings for the happy condition, and additionally right insula for the neutral condition, survived multiple comparison correction. Exploratory analyses did not reveal additional regions of group differences. This study provides evidence for decreased functional connectivity between the amygdala and anterior paralimbic cortices in adolescents with BD. This suggests that amygdala-anterior paralimbic connectivity abnormalities are early features of BD that emerge at least by adolescence in the disorder. Public Library of Science 2012-11-21 /pmc/articles/PMC3503984/ /pubmed/23185566 http://dx.doi.org/10.1371/journal.pone.0050177 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Wang, Fei
Bobrow, Laurel
Liu, Jie
Spencer, Linda
Blumberg, Hilary P.
Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title_full Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title_fullStr Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title_full_unstemmed Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title_short Corticolimbic Functional Connectivity in Adolescents with Bipolar Disorder
title_sort corticolimbic functional connectivity in adolescents with bipolar disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503984/
https://www.ncbi.nlm.nih.gov/pubmed/23185566
http://dx.doi.org/10.1371/journal.pone.0050177
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