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Variants of the P3 event-related potential operate as indicators of distinct mechanisms contributing to problematic alcohol use.
Joyner, Keanan J; Patrick, Christopher J; Morris, David H; McCarthy, Denis M; Bartholow, Bruce D.
Afiliação
  • Joyner KJ; Department of Psychology, University of California, Berkeley, CA, USA.
  • Patrick CJ; Department of Psychology, Florida State University, Tallahassee, FL, USA.
  • Morris DH; Alvin J. Siteman Cancer Center, Washington University in St. Louis, St. Louis, MO, USA.
  • McCarthy DM; Department of Psychological Sciences, University of Missouri, Columbia, MO, USA.
  • Bartholow BD; Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA, USA. bruce-bartholow@uiowa.edu.
Article em En | MEDLINE | ID: mdl-38734817
ABSTRACT
Considerable research has linked relative reduction in the amplitude of the P3 event-related potential (ERP) during cognitive task performance (i.e., Target-P3) with increased risk of alcohol-related problems. A separate literature indicates that a relative increase in the amplitude of the P3 elicited by cues signaling alcohol availability (i.e., ACR-P3) also is associated with alcohol use and problems. To date, no research has integrated these seemingly discrepant findings. Here, we aimed to demonstrate that P3 amplitudes elicited in different task contexts reflect distinct domains of functioning relevant to problematic alcohol involvement (PAI), and therefore can inform heterogeneity in the etiology of PAI. 156 emerging adults (61% women; 88% White/Non-Hispanic) completed a mental rotation task and a picture-viewing task while ERPs were recorded. Participants also completed questionnaire measures of trait disinhibition, alcohol use, and alcohol-related problems. Findings from regression analyses indicated that (a) Target-P3 was negatively associated and ACR-P3 was positively associated with a PAI latent variable; (b) the two P3s accounted for unique variance in PAI, beyond that accounted for by recent drinking; and (c) the association between Target-P3 and PAI-but not ACR-P3 and PAI-was statistically mediated by trait disinhibition. The present findings highlight the unique contributions of distinct functional domains associated with disinhibition and incentive salience in the etiology of PAI. Moreover, findings are consistent with a nuanced understanding of the P3 ERP, whereby its specific meaning varies according to the task context in which it is elicited.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuropsychopharmacology Assunto da revista: NEUROLOGIA / PSICOFARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuropsychopharmacology Assunto da revista: NEUROLOGIA / PSICOFARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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