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Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals

Alcohol dependence is a chronic relapsing illness. Alcohol and stress cues have consistently been shown to increase craving and relapse risk in recovering alcohol dependent (AUD) patients. However, differences in functional connectivity in response to these cues have not been studied using data-driv...

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Autores principales: Zakiniaeiz, Yasmin, Scheinost, Dustin, Seo, Dongju, Sinha, Rajita, Constable, R. Todd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144743/
https://www.ncbi.nlm.nih.gov/pubmed/27981033
http://dx.doi.org/10.1016/j.nicl.2016.10.019
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author Zakiniaeiz, Yasmin
Scheinost, Dustin
Seo, Dongju
Sinha, Rajita
Constable, R. Todd
author_facet Zakiniaeiz, Yasmin
Scheinost, Dustin
Seo, Dongju
Sinha, Rajita
Constable, R. Todd
author_sort Zakiniaeiz, Yasmin
collection PubMed
description Alcohol dependence is a chronic relapsing illness. Alcohol and stress cues have consistently been shown to increase craving and relapse risk in recovering alcohol dependent (AUD) patients. However, differences in functional connectivity in response to these cues have not been studied using data-driven approaches. Here, voxel-wise connectivity is used in a whole-brain investigation of functional connectivity differences associated with alcohol and stress cues and to examine whether these differences are related to subsequent relapse. In Study 1, 45, 4- to 8-week abstinent, recovering AUD patients underwent functional magnetic resonance imaging during individualized imagery of alcohol, stress, and neutral cues. Relapse measures were collected prospectively for 90 days post-discharge from inpatient treatment. AUD patients showed blunted anterior (ACC), mid (MCC) and posterior cingulate cortex (PCC), voxel-wise connectivity responses to stress compared to neutral cues and blunted PCC response to alcohol compared to neutral cues. Using Cox proportional hazard regression, weaker connectivity in ACC and MCC during neutral exposure was associated with longer time to relapse (better recovery outcome). Similarly, greater connectivity in PCC during alcohol-cue compared to stress cue was associated with longer time to relapse. In Study 2, a sub-group of 30 AUD patients were demographically-matched to 30 healthy control (HC) participants for group comparisons. AUD compared to HC participants showed reduced cingulate connectivity during alcohol and stress cues. Using novel data-driven approaches, the cingulate cortex emerged as a key region in the disruption of functional connectivity during alcohol and stress-cue processing in AUD patients and as a marker of subsequent alcohol relapse.
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spelling pubmed-51447432016-12-15 Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals Zakiniaeiz, Yasmin Scheinost, Dustin Seo, Dongju Sinha, Rajita Constable, R. Todd Neuroimage Clin Regular Article Alcohol dependence is a chronic relapsing illness. Alcohol and stress cues have consistently been shown to increase craving and relapse risk in recovering alcohol dependent (AUD) patients. However, differences in functional connectivity in response to these cues have not been studied using data-driven approaches. Here, voxel-wise connectivity is used in a whole-brain investigation of functional connectivity differences associated with alcohol and stress cues and to examine whether these differences are related to subsequent relapse. In Study 1, 45, 4- to 8-week abstinent, recovering AUD patients underwent functional magnetic resonance imaging during individualized imagery of alcohol, stress, and neutral cues. Relapse measures were collected prospectively for 90 days post-discharge from inpatient treatment. AUD patients showed blunted anterior (ACC), mid (MCC) and posterior cingulate cortex (PCC), voxel-wise connectivity responses to stress compared to neutral cues and blunted PCC response to alcohol compared to neutral cues. Using Cox proportional hazard regression, weaker connectivity in ACC and MCC during neutral exposure was associated with longer time to relapse (better recovery outcome). Similarly, greater connectivity in PCC during alcohol-cue compared to stress cue was associated with longer time to relapse. In Study 2, a sub-group of 30 AUD patients were demographically-matched to 30 healthy control (HC) participants for group comparisons. AUD compared to HC participants showed reduced cingulate connectivity during alcohol and stress cues. Using novel data-driven approaches, the cingulate cortex emerged as a key region in the disruption of functional connectivity during alcohol and stress-cue processing in AUD patients and as a marker of subsequent alcohol relapse. Elsevier 2016-11-01 /pmc/articles/PMC5144743/ /pubmed/27981033 http://dx.doi.org/10.1016/j.nicl.2016.10.019 Text en © 2016 The Authors 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
Zakiniaeiz, Yasmin
Scheinost, Dustin
Seo, Dongju
Sinha, Rajita
Constable, R. Todd
Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title_full Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title_fullStr Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title_full_unstemmed Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title_short Cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
title_sort cingulate cortex functional connectivity predicts future relapse in alcohol dependent individuals
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144743/
https://www.ncbi.nlm.nih.gov/pubmed/27981033
http://dx.doi.org/10.1016/j.nicl.2016.10.019
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