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    Reward Sensitivity of ACC as an Intermediate Phenotype between DRD4-521T and Substance Misuse

    Access Status
    Fulltext not available
    Authors
    Baker, T.
    Stockwell, Tim
    Barnes, G.
    Haesevoets, R.
    Holroyd, C.
    Date
    2016
    Type
    Journal Article
    
    Metadata
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    Citation
    Baker, T. and Stockwell, T. and Barnes, G. and Haesevoets, R. and Holroyd, C. 2016. Reward Sensitivity of ACC as an Intermediate Phenotype between DRD4-521T and Substance Misuse. Journal of Cognitive Neuroscience. 28 (3): pp. 460-471.
    Source Title
    Journal of Cognitive Neuroscience
    DOI
    10.1162/jocn_a_00905
    ISSN
    0898-929X
    School
    National Drug Research Institute (NDRI)
    URI
    http://hdl.handle.net/20.500.11937/30511
    Collection
    • Curtin Research Publications
    Abstract

    The development and expression of the midbrain dopamine system is determined in part by genetic factors that vary across individuals such that dopamine-related genes are partly responsible for addiction vulnerability. However, a complete account of how dopamine-related genes predispose individuals to drug addiction remains to be developed. Adopting an intermediate phenotype approach, we investigated whether reward-related electrophysiological activity of ACC—a cortical region said to utilize dopamine reward signals to learn the value of extended, context-specific sequences of goal-directed behaviors—mediates the influence of multiple dopamine-related functional polymorphisms over substance use. We used structural equation modeling to examine whether two related electrophysiological phenomena associated with the control and reinforcement learning functions of ACC—theta power and the reward positivity— mediated the relationship between the degree of substance misuse and genetic polymorphisms that regulate dopamine processing in frontal cortex. Substance use data were collected from 812 undergraduate students. One hundred ninety-six returned on a subsequent day to participate in an electrophysiological experiment and to provide saliva samples for DNA analysis. We found that these electrophysiological signals mediated a relationship between the DRD4-521T dopamine receptor genotype and substance misuse. Our results provide a theoretical framework that bridges the gap between genes and behavior in drug addiction and illustrate how future interventions might be individually tailored for specific genetic and neurocognitive profiles.

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