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Confidence and psychosis: a neuro-computational account of contingency learning disruption by NMDA blockade.


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Authors

Vinckier, F 
Gaillard, R 
Palminteri, S 
Rigoux, L 
Salvador, A 

Abstract

A state of pathological uncertainty about environmental regularities might represent a key step in the pathway to psychotic illness. Early psychosis can be investigated in healthy volunteers under ketamine, an NMDA receptor antagonist. Here, we explored the effects of ketamine on contingency learning using a placebo-controlled, double-blind, crossover design. During functional magnetic resonance imaging, participants performed an instrumental learning task, in which cue-outcome contingencies were probabilistic and reversed between blocks. Bayesian model comparison indicated that in such an unstable environment, reinforcement learning parameters are downregulated depending on confidence level, an adaptive mechanism that was specifically disrupted by ketamine administration. Drug effects were underpinned by altered neural activity in a fronto-parietal network, which reflected the confidence-based shift to exploitation of learned contingencies. Our findings suggest that an early characteristic of psychosis lies in a persistent doubt that undermines the stabilization of behavioral policy resulting in a failure to exploit regularities in the environment.

Description

Keywords

Adult, Bayes Theorem, Conditioning, Classical, Double-Blind Method, Female, Humans, Ketamine, Learning, Magnetic Resonance Imaging, Male, Psychoses, Substance-Induced, Psychotic Disorders, Receptors, N-Methyl-D-Aspartate

Journal Title

Mol Psychiatry

Conference Name

Journal ISSN

1359-4184
1476-5578

Volume Title

Publisher

Springer Science and Business Media LLC
Sponsorship
Medical Research Council (G0001354)
Medical Research Council (MC_UU_12012/5/B)
Wellcome Trust (093875/Z/10/Z)
Wellcome Trust (095692/Z/11/Z)
Medical Research Council (G1000183)
Medical Research Council (MC_UU_12012/5)
Medical Research Council (MC_PC_12012)
FV was supported by the Groupe Pasteur Mutualité. RG was supported by the Fondation pour la Recherche Médicale and the Fondation Bettencourt Schueller. SP is supported by a Marie Curie Intra-European fellowship (FP7-PEOPLE-2012-IEF). AF was supported by National Health and Medical Research Council grants (IDs : 1050504 and 1066779) and an Australian Research Council Future Fellowship (ID: FT130100589). This work was supported by the Wellcome Trust and the Bernard Wolfe Health Neuroscience Fund.