Literature DB >> 28935223

Testing the effects of adolescent alcohol use on adult conflict-related theta dynamics.

Jeremy Harper1, Stephen M Malone2, William G Iacono2.   

Abstract

OBJECTIVE: Adolescent alcohol use (AAU) is associated with brain anomalies, but less is known about long-term neurocognitive effects. Despite theoretical models linking AAU to diminished cognitive control, empirical work testing this relationship with specific cognitive control neural correlates (e.g., prefrontal theta-band EEG dynamics) remains scarce. A longitudinal twin design was used to test the hypothesis that greater AAU is associated with reduced conflict-related EEG theta-band dynamics in adulthood, and to examine the genetic/environmental etiology of this association.
METHODS: In a large (N=718) population-based prospective twin sample, AAU was assessed at ages 11/14/17. Twins completed a flanker task at age 29 to elicit EEG theta-band medial frontal cortex (MFC) power and medial-dorsal prefrontal cortex (MFC-dPFC) connectivity. Two complementary analytic methods (cotwin control analysis; biometric modeling) were used to disentangle the genetic/shared environmental risk towards AAU from possible alcohol exposure effects on theta dynamics.
RESULTS: AAU was negatively associated with adult cognitive control-related theta-band MFC power and MFC-dPFC functional connectivity. Genetic influences primarily underlie these associations.
CONCLUSIONS: Findings provide strong evidence that genetic factors underlie the comorbidity between AAU and diminished cognitive control-related theta dynamics in adulthood. SIGNIFICANCE: Conflict-related theta-band dynamics appear to be candidate brain-based endophenotypes/mechanisms for AAU.
Copyright © 2017 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Adolescent alcohol use; Cognitive control; Cotwin control; Endophenotype; Functional connectivity; Theta

Mesh:

Year:  2017        PMID: 28935223      PMCID: PMC5675801          DOI: 10.1016/j.clinph.2017.08.019

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


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