Reduced Left Executive Control Network Functional Connectivity Is Associated with Alcohol Use Disorders

Background Altered functional connectivity in critical networks has been associated with chronic alcohol abuse. In turn, changes in connectivity in executive control networks (ECNs) may undermine the ability to control alcohol consumption. It was hypothesized that network connectivity would be reduc...

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Published in:Alcoholism, clinical and experimental research Vol. 38; no. 9; pp. 2445 - 2453
Main Authors: Weiland, Barbara J., Sabbineni, Amithrupa, Calhoun, Vince D., Welsh, Robert C., Bryan, Angela D., Jung, Rex E., Mayer, Andrew R., Hutchison, Kent E.
Format: Journal Article
Language:English
Published: England Blackwell Publishing Ltd 01-09-2014
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Summary:Background Altered functional connectivity in critical networks has been associated with chronic alcohol abuse. In turn, changes in connectivity in executive control networks (ECNs) may undermine the ability to control alcohol consumption. It was hypothesized that network connectivity would be reduced in individuals with problematic alcohol use (ALC) compared with controls and that diminished network connectivity would be associated with greater failure to control drinking. Methods Resting‐state functional magnetic resonance imaging was analyzed to identify 14 previously identified intrinsic connectivity networks (ICNs) using a priori regions of interest in cases ranging from binge drinkers to those with severe alcohol use disorder, as well as control subjects. Analyses tested for differences in network connectivity strength between 255 ALC cases and 87 age‐ and gender‐matched controls. Further, structural equation analysis, using 383 ALC cases, tested whether functional connectivity strength mediated the relationship between years of regular drinking and alcohol problems. Results The age‐ and gender‐matched analysis showed that ALC had significantly lower network connectivity strength than controls in the left executive control (LECN), basal ganglia, and primary visual networks. For all ALC, LECN connectivity strength is negatively correlated with failed control and alcohol disorder severity. Edges connecting parietal regions with dorsolateral prefrontal, middle frontal, and temporal regions within the LECN drove these relationships. A positive association between years of drinking and severity of alcohol problems was mediated by reduced ECN connectivity. Conclusions This study reports relationships between network strength and problematic alcohol use, suggesting that chronic drinking negatively impacts brain connectivity, specifically in the LECN. Altered functional connectivity, related to chronic alcohol abuse, may contribute to the etiology of alcohol dependence and relapse.
Bibliography:National Institute of Neurological Disorders and Stroke (NINDS) - No. R01052514
ark:/67375/WNG-5BRW8WFN-T
Data S1. Methods and results. Figure S1. Regions with functional connectivity to the seed region in left parietal lobe (blue) representing the left executive control network. Color bar represents t-scores. Figure S2. Regions with functional connectivity to the seed region in bilateral thalami (blue) representing the basal ganglia network. Figure S3. Regions with functional connectivity to the seed region in supplementary motor area (blue) representing the sensorimotor network. Figure S4. Regions with functional connectivity to the seed region in V1 (blue) representing the primary visual network. Figure S5. Regions with functional connectivity to the seed region in left parietal lobe (blue), which were negatively correlated with failure to control alcohol consumption.
ArticleID:ACER12505
Brain and Behavior Foundation (NARSAD) Young Investigator
istex:FEA0CC331C64954F1D70ADF10127BE27A9B550F5
NIDA - No. R01DA025074
National Institute on Drug Abuse (NIDA) - No. K01 DA031755
National Institute of Biomedical Imaging and Bioengineering (NIBIB) - No. 2R01EB000840
John Templeton Foundation
National Institute on Alcohol Abuse and Alcoholism (NIAAA) - No. R01AA012238
ISSN:0145-6008
1530-0277
DOI:10.1111/acer.12505