Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109777
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dc.contributor.authorHowell, Nicholas A.-
dc.contributor.authorWorbe, Yulia-
dc.contributor.authorLange, Iris-
dc.contributor.authorTait, Roger-
dc.contributor.authorIrvine, Michael-
dc.contributor.authorBanca, Paula-
dc.contributor.authorHarrison, Neil A-
dc.contributor.authorBullmore, Edward T.-
dc.contributor.authorHutchison, William D.-
dc.contributor.authorVoon, Valerie-
dc.date.accessioned2023-10-26T09:34:33Z-
dc.date.available2023-10-26T09:34:33Z-
dc.date.issued2013-
dc.identifier.issn1932-6203pt
dc.identifier.urihttps://hdl.handle.net/10316/109777-
dc.description.abstractBackground: 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. Clusterextent 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.pt
dc.language.isoengpt
dc.publisherPublic Library of Sciencept
dc.relationUnilever/Lipton Graduate Fellowship in Neuroscience and a University of Toronto Open Fellowshippt
dc.relationWellcome Trust (WT)pt
dc.relationFyssen Foundation and MRC Studentshippt
dc.relationWT and MRC grant.pt
dc.relationNIHR Cambridge Biomedical Research Centre, Cambridgeshire & Peterborough NHS Foundation Trust Cambridge UKpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAdolescentpt
dc.subject.meshAdultpt
dc.subject.meshBasal Gangliapt
dc.subject.meshBinge Drinkingpt
dc.subject.meshCase-Control Studiespt
dc.subject.meshHumanspt
dc.subject.meshYoung Adultpt
dc.titleIncreased ventral striatal volume in college-aged binge drinkerspt
dc.typearticle-
degois.publication.firstPagee74164pt
degois.publication.issue9pt
degois.publication.titlePLoS ONEpt
dc.peerreviewedyespt
dc.identifier.doi10.1371/journal.pone.0074164pt
degois.publication.volume8pt
dc.date.embargo2013-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
Appears in Collections:I&D IBILI - Artigos em Revistas Internacionais
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