Journal article
Mesocorticolimbic system reactivity to alcohol use-related visual cues as a function of alcohol sensitivity phenotype: A pilot fMRI study
Addiction neuroscience, Vol.11, 100156
06/01/2024
DOI: 10.1016/j.addicn.2024.100156
PMCID: PMC11209874
PMID: 38938269
Abstract
Low sensitivity (LS) to alcohol is a risk factor for alcohol use disorder (AUD). Compared to peers with high sensitivity (HS), LS individuals drink more, report more problems, and exhibit potentiated alcohol cue reactivity (ACR). Heightened ACR suggests LS confers AUD risk via incentive sensitization, which is thought to take place in the mesocorticolimbic system. This study examined neural ACR in LS and HS individuals. Young adults (N = 32, Mage=20.3) were recruited based on the Alcohol Sensitivity Questionnaire (HS: n = 16; LS: n = 16; 9 females/group). Participants completed an event-related fMRI ACR task. Group LS had higher ACR in left ventrolateral prefrontal cortex than group HS. In group LS, ACR in left caudomedial orbitofrontal cortex or left putamen was low at low alcohol use levels and high at heavier or more problematic alcohol use levels, whereas the opposite was true in group HS. Alcohol use level also was associated with the level of ACR in left substantia nigra among males in group LS. Taken together, results suggest elevated mesocorticolimbic ACR among LS individuals, especially those using alcohol at hazardous levels. Future studies with larger samples are warranted to determine the neurobiological loci underlying LS-based amplified ACR and AUD risk.
Details
- Title: Subtitle
- Mesocorticolimbic system reactivity to alcohol use-related visual cues as a function of alcohol sensitivity phenotype: A pilot fMRI study
- Creators
- Roberto U. CofresíSpencer Upton - University of MissouriAlexander A. Brown - University of MissouriThomas M. Piasecki - University of Wisconsin–MadisonBruce D. Bartholow - University of IowaBrett Froeliger
- Resource Type
- Journal article
- Publication Details
- Addiction neuroscience, Vol.11, 100156
- DOI
- 10.1016/j.addicn.2024.100156
- PMID
- 38938269
- PMCID
- PMC11209874
- NLM abbreviation
- Addict Neurosci
- eISSN
- 2772-3925
- Publisher
- Elsevier
- Grant note
- University of Missouri Cognitive Neuroscience Systems Core Facility Board of DirectorsNIH: AA013526, AA025451, AA029169 NIH Diversity Supplement: AA025451-[04/05]S1
Funding for the project was provided by an internal seed grant from the University of Missouri Cognitive Neuroscience Systems Core Facility Board of Directors. BDB and TMP's contributions were supported by NIH AA025451. RUC's contributions were supported by: NIH T32 (AA013526) , NIH Diversity Supplement (AA025451-[04/05]S1) , and NIH K99 (AA029169) . Funding sources had no role in the research other than financial support.
- Language
- English
- Date published
- 06/01/2024
- Academic Unit
- Psychological and Brain Sciences; Iowa Neuroscience Institute
- Record Identifier
- 9984626030602771
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