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Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder
Previous research suggests the amplitude of the P3 event-related potential (ERP) response reflects the incentive value of the eliciting stimulus, and that individuals with trait-like lower sensitivity (LS) to the acute effects of alcohol, a potent risk factor for alcohol use disorder (AUD), tend to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681121/ https://www.ncbi.nlm.nih.gov/pubmed/36425356 http://dx.doi.org/10.1016/j.addicn.2022.100041 |
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author | Cofresí, Roberto U. Piasecki, Thomas M. Bartholow, Bruce D. |
author_facet | Cofresí, Roberto U. Piasecki, Thomas M. Bartholow, Bruce D. |
author_sort | Cofresí, Roberto U. |
collection | PubMed |
description | Previous research suggests the amplitude of the P3 event-related potential (ERP) response reflects the incentive value of the eliciting stimulus, and that individuals with trait-like lower sensitivity (LS) to the acute effects of alcohol, a potent risk factor for alcohol use disorder (AUD), tend to show exaggerated P3 ERP responses to alcohol beverage cues (compared to their peers with higher sensitivity; HS). No prior research has examined trajectories of the cue-elicited P3 response across repeated trials of nonreinforced cue presentations. Characterizing these trajectories can be informative as to potential mechanisms linking LS with increased AUD risk. Here, we tested whether individual differences in alcohol sensitivity are associated with different trial-by-trial trajectories of the P3 elicited by alcohol and nonalcohol reward cues (infrequent oddball/target stimuli) using a large sample of emerging adults (M(age) = 19.53; N = 287; 55% female; 86% White; 90% right-handed) stratified for alcohol sensitivity. Multilevel models adjusted for age, sex, handedness, and alcohol use indicated that: (i) the P3 response to alcohol and nonalcohol reward cues alike sensitized (i.e., increased) across trials; (ii) across the task, the P3 response to alcohol cues was larger for the LS than the HS phenotype; and (iii) the P3 difference score (alcohol - nonalcohol) was larger for the LS than HS phenotype only across the first half of task. Findings suggest that whereas incentive value attribution may be a mechanism for alcohol cue-triggered attentional biases for both LS and HS individuals, LS individuals more consistently over-attribute incentive value to alcohol cues. |
format | Online Article Text |
id | pubmed-9681121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-96811212022-12-01 Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder Cofresí, Roberto U. Piasecki, Thomas M. Bartholow, Bruce D. Addict Neurosci Article Previous research suggests the amplitude of the P3 event-related potential (ERP) response reflects the incentive value of the eliciting stimulus, and that individuals with trait-like lower sensitivity (LS) to the acute effects of alcohol, a potent risk factor for alcohol use disorder (AUD), tend to show exaggerated P3 ERP responses to alcohol beverage cues (compared to their peers with higher sensitivity; HS). No prior research has examined trajectories of the cue-elicited P3 response across repeated trials of nonreinforced cue presentations. Characterizing these trajectories can be informative as to potential mechanisms linking LS with increased AUD risk. Here, we tested whether individual differences in alcohol sensitivity are associated with different trial-by-trial trajectories of the P3 elicited by alcohol and nonalcohol reward cues (infrequent oddball/target stimuli) using a large sample of emerging adults (M(age) = 19.53; N = 287; 55% female; 86% White; 90% right-handed) stratified for alcohol sensitivity. Multilevel models adjusted for age, sex, handedness, and alcohol use indicated that: (i) the P3 response to alcohol and nonalcohol reward cues alike sensitized (i.e., increased) across trials; (ii) across the task, the P3 response to alcohol cues was larger for the LS than the HS phenotype; and (iii) the P3 difference score (alcohol - nonalcohol) was larger for the LS than HS phenotype only across the first half of task. Findings suggest that whereas incentive value attribution may be a mechanism for alcohol cue-triggered attentional biases for both LS and HS individuals, LS individuals more consistently over-attribute incentive value to alcohol cues. 2022-12 2022-10-28 /pmc/articles/PMC9681121/ /pubmed/36425356 http://dx.doi.org/10.1016/j.addicn.2022.100041 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) |
spellingShingle | Article Cofresí, Roberto U. Piasecki, Thomas M. Bartholow, Bruce D. Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title | Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title_full | Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title_fullStr | Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title_full_unstemmed | Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title_short | Acute sensitization of the P3 event-related potential response to beverage images and the risk for alcohol use disorder |
title_sort | acute sensitization of the p3 event-related potential response to beverage images and the risk for alcohol use disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681121/ https://www.ncbi.nlm.nih.gov/pubmed/36425356 http://dx.doi.org/10.1016/j.addicn.2022.100041 |
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