Increased Nucleus Accumbens Volume in College Binge Drinkers - Preliminary Evidence From Manually Segmented MRI Analysis
Author(s) -
Sónia S. Sousa,
Adriana Sampaio,
Eduardo LópezCaneda,
Clothilde Bec,
Óscar F. Gonçalves,
Alberto Crego
Publication year - 2020
Publication title -
frontiers in psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.363
H-Index - 67
ISSN - 1664-0640
DOI - 10.3389/fpsyt.2019.01005
Subject(s) - nucleus accumbens , basal ganglia , psychology , addiction , caudate nucleus , amygdala , neuroscience , extended amygdala , magnetic resonance imaging , binge drinking , alcohol dependence , clinical psychology , medicine , alcohol , dopamine , central nervous system , alcohol consumption , biology , radiology , biochemistry
Binge drinking (BD) is characterized by high alcohol intake in a short time followed by periods of withdrawal. This pattern is very common during adolescence and early adulthood, a developmental stage marked by the maturation of the fronto-striatal networks. The basal ganglia, specifically the nucleus accumbens (NAcc) and the caudate nucleus (CN), are part of the fronto-striatal limbic circuit involved in reward processes underlying addictive behaviors. Abnormal NAcc and CN morphometry has been noted in alcoholics and other drug abusers, however the effects of BD on these subcortical regions have been poorly explored. Accordingly, the main goal of the present study was to address potential morphological alterations in the NAcc and CN in a sample of college binge drinkers (BDs). Method Manual segmentation of the NAcc and the CN was performed in Magnetic Resonance Imaging (MRI) of 20 college BDs and 16 age-matched alcohol abstainers (18–23 years-old). Results A two-way mixed ANOVA revealed no group differences in the volumetry of the CN, whereas increased NAcc volume was observed in the BD group when compared to their abstinent control peers. Discussion These findings are in line with previous automatically segmented MRI reports highlighting abnormalities in a key region involved in drug rewarding processes in BDs.
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