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Increased Ventral Striatal Volume in College-Aged Binge Drinkers
Author(s) -
Nicholas A. Howell,
Yulia Worbe,
Iris Lange,
Roger Tait,
Michael A. Irvine,
Paula Banca,
Neil A. Harrison,
Edward T. Bullmore,
William D. Hutchison,
Valerie Voon
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0074164
Subject(s) - grey matter , voxel based morphometry , binge drinking , amygdala , ventral striatum , psychology , population , striatum , alcohol use disorders identification test , medicine , basal ganglia , neuroscience , clinical psychology , magnetic resonance imaging , central nervous system , white matter , poison control , injury prevention , environmental health , dopamine , radiology
Background Binge drinking is a serious public health issue associated with cognitive, physiological, and anatomical differences from healthy individuals. No studies, however, have reported subcortical grey matter differences in this population. To address this, we compared the grey matter volumes of college-age binge drinkers and healthy controls, focusing on the ventral striatum, hippocampus and amygdala. Method T1-weighted images of 19 binge drinkers and 19 healthy volunteers were analyzed using voxel-based morphometry. Structural data were also covaried with Alcohol Use Disorders Identification Test (AUDIT) scores. Cluster-extent threshold and small volume corrections were both used to analyze imaging data. Results Binge drinkers had significantly larger ventral striatal grey matter volumes compared to controls. There were no between group differences in hippocampal or amygdalar volume. Ventral striatal, amygdalar, and hippocampal volumes were also negatively related to AUDIT scores across groups. Conclusions Our findings stand in contrast to the lower ventral striatal volume previously observed in more severe forms of alcohol use disorders, suggesting that college-age binge drinkers may represent a distinct population from those groups. These findings may instead represent early sequelae, compensatory effects of repeated binge and withdrawal, or an endophenotypic risk factor.

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