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Variants of the P3 event-related potential operate as indicators of distinct mechanisms contributing to problematic alcohol use
Journal article   Open access   Peer reviewed

Variants of the P3 event-related potential operate as indicators of distinct mechanisms contributing to problematic alcohol use

Keanan J Joyner, Christopher J Patrick, David H Morris, Denis M McCarthy and Bruce D Bartholow
Neuropsychopharmacology (New York, N.Y.), Vol.49(12), pp.1819-1826
11/2024
DOI: 10.1038/s41386-024-01874-7
PMCID: PMC11473729
PMID: 38734817
url
https://pmc.ncbi.nlm.nih.gov/articles/PMC11473729/pdf/41386_2024_Article_1874.pdfView
Open Access

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.

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