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Polygenic risk of psychosis and ventral striatal activation during reward processing in healthy adolescents

Authors :
Lancaster, Thomas M.
Linden, David E.
Tansey, Katherine E.
Banaschewski, Tobias
Bokde, Arun L.W.
Bromberg, Uli
Büchel, Christian
Cattrell, Anna
Conrod, Patricia J.
Flor, Herta
Frouin, Vincent
Gallinat, Jürgen
Garavan, Hugh
Gowland, Penny A.
Heinz, Andreas
Ittermann, Bernd
Martinot, Jean-Luc
Paillère Martinot, Marie-Laure
Artiges, Eric
Lemaitre, Herve
Nees, Frauke
Orfanos, Dimitri Papadopoulos
Paus, Tomáš
Poustka, Luise
Smolka, Michael N.
Vetter, Nora C.
Jurk, Sarah
Mennigen, Eva
Walter, Henrik
Whelan, Robert
Schumann, Gunter
Lancaster, Thomas M.
Linden, David E.
Tansey, Katherine E.
Banaschewski, Tobias
Bokde, Arun L.W.
Bromberg, Uli
Büchel, Christian
Cattrell, Anna
Conrod, Patricia J.
Flor, Herta
Frouin, Vincent
Gallinat, Jürgen
Garavan, Hugh
Gowland, Penny A.
Heinz, Andreas
Ittermann, Bernd
Martinot, Jean-Luc
Paillère Martinot, Marie-Laure
Artiges, Eric
Lemaitre, Herve
Nees, Frauke
Orfanos, Dimitri Papadopoulos
Paus, Tomáš
Poustka, Luise
Smolka, Michael N.
Vetter, Nora C.
Jurk, Sarah
Mennigen, Eva
Walter, Henrik
Whelan, Robert
Schumann, Gunter

Abstract

Importance: Psychotic disorders are characterized by attenuated activity in the brain’s valuation system in key reward processing areas, such as the ventral striatum (VS), as measured with functional magnetic resonance imaging. Objective: To examine whether common risk variants for psychosis are associated with individual variation in the VS. Design, setting, and participants: A cross-sectional study of a large cohort of adolescents from the IMAGEN study (a European multicenter study of reinforcement sensitivity in adolescents) was performed from March 1, 2008, through December 31, 2011. Data analysis was conducted from October 1, 2015, to January 9, 2016. Polygenic risk profile scores (RPSs) for psychosis were generated for 1841 healthy adolescents. Sample size and characteristics varied across regression analyses, depending on mutual information available (N = 1524-1836). Main outcomes and measures: Reward-related brain function was assessed with blood oxygen level dependency (BOLD) in the VS using the monetary incentive delay (MID) task, distinguishing reward anticipation and receipt. Behavioral impulsivity, IQ, MID task performance, and VS BOLD were regressed against psychosis RPS at 4 progressive P thresholds (P < .01, P < .05, P < .10, and P < .50 for RPS models 1-4, respectively). Results: In a sample of 1841 healthy adolescents (mean age, 14.5 years; 906 boys and 935 girls), we replicated an association between increasing psychosis RPS and reduced IQ (matrix reasoning: corrected P = .003 for RPS model 2, 0.4%variance explained), supporting the validity of the psychosis RPS models. We also found a nominally significant association between increased psychosis RPS and reduced MID task performance (uncorrected P = .03 for RPS model 4, 0.2%variance explained). Our main finding was a positive association between psychosis RPS and VS BOLD during reward anticipation at all 4 psychosis RPS models and for 2 P thresholds for reward receipt (RPS models 1 and 3), correct

Details

Database :
OAIster
Notes :
doi:10.1001/jamapsychiatry.2016.1135
Publication Type :
Electronic Resource
Accession number :
edsoai.on1358466484
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1001.jamapsychiatry.2016.1135