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Modulation of orbitofrontal-striatal reward activity by dopaminergic functional polymorphisms contributes to a predisposition to alcohol misuse in early adolescence

Research output: Contribution to journalArticle

Travis E. Baker, Natalie Castellanos-Ryan, Gunter Schumann, Anna Cattrell, Herta Flor, Frauke Nees, Tobias Banaschewski, Arun Bokde, Rob Whelan, Christian Buechel, Uli Bromberg, Dimitri Papadopoulos Orfanos, Juergen Gallinat, Hugh Garavan, Andreas Heinz, Henrik Walter, Rüdiger Brühl, Penny Gowland, Tomáš Paus, Luise Poustka & 7 more Jean Luc Martinot, Herve Lemaitre, Eric Artiges, Marie Laure Paillère Martinot, Michael N. Smolka, Patricia Conrod, The IMAGEN Consortium

Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalPsychological Medicine
Early online date18 Jun 2018
DOIs
Publication statusE-pub ahead of print - 18 Jun 2018

King's Authors

Abstract

Background: Abnormalities in reward circuit function are considered a core feature of addiction. Yet, it is still largely unknown whether these abnormalities stem from chronic drug use, a genetic predisposition, or both. Methods: In the present study, we investigated this issue using a large sample of adolescent children by applying structural equation modeling to examine the effects of several dopaminergic polymorphisms of the D1 and D2 receptor type on the reward function of the ventral striatum (VS) and orbital frontal cortex (OFC), and whether this relationship predicted the propensity to engage in early alcohol misuse behaviors at 14 years of age and again at 16 years of age. Results: The results demonstrated a regional specificity with which the functional polymorphism rs686 of the D1 dopamine receptor (DRD1) gene and Taq1A of the ANKK1 gene influenced medial and lateral OFC activation during reward anticipation, respectively. Importantly, our path model revealed a significant indirect relationship between the rs686 of the DRD1 gene and early onset of alcohol misuse through a medial OFC × VS interaction. Conclusions: These findings highlight the role of D1 and D2 in adjusting reward-related activations within the mesocorticolimbic circuitry, as well as in the susceptibility to early onset of alcohol misuse.

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