4.6 Article

Neurophysiological correlates of alcohol-specific inhibition in alcohol use disorder and its association with craving and relapse

Journal

CLINICAL NEUROPHYSIOLOGY
Volume 132, Issue 6, Pages 1290-1301

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.clinph.2021.02.389

Keywords

Inhibitory control; Event-Related Potentials; Go; NoGo task; Alcohol Use Disorder; Relapse; Craving

Funding

  1. Swiss National Science Foundation (SNSF) [105319_159286]
  2. Swiss National Science Foundation (SNF) [105319_159286] Funding Source: Swiss National Science Foundation (SNF)

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This study investigated neurophysiological correlates of inhibitory control in patients with Alcohol Use Disorder, finding that the response inhibition conflict may be enhanced in alcohol-related contexts and individuals can be differentiated between relapsers and abstainers based on specific ERP components.
Objective: This study investigates neurophysiological correlates of general and alcohol-specific inhibitory control in patients with Alcohol Use Disorder (AUD), focusing on its association with individual craving levels and with relapse at three-month follow-up. Methods: 59 abstinent AUD patients and 20 healthy controls performed a Go/NoGo task incorporating alcohol-related and neutral stimuli during 64-channel electroencephalography (EEG) recording, yielding four event-related potentials (ERP) per participant (NoGo-Alcohol, Go-Alcohol, NoGo-Neutral, Go Neutral). Whole-scalp randomization-based statistics assessed effects of the factors group (patients/controls or relapsers/abstainers), craving level, response type (NoGo/Go) and picture type (alcohol/neutral) on topography and signal strength of the ERP components N2 and P3. Results: No differences on group level were observed between patients and controls. However, analyses incorporating individual craving indicated that the topographic difference between alcohol-related and neutral NoGo-N2 components increased with craving. Moreover, topographic differences in the alcohol-related and neutral NoGo-P3 component allowed for differentiation between relapsers and abstainers. Conclusions: In alcohol-related contexts, the response inhibition conflict reflected in the NoGo-N2 seems enhanced in patients with high craving. The inhibition-sensitive NoGo-P3 varies in relapsers but not in abstainers between neutral and alcohol-related contexts. Significance: In AUD patients, neurophysiological correlates of inhibition vary with alcohol-related contexts and craving, and might be indicative of relapse risk. (c) 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

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