Distinct alterations in probabilistic reversal learning across at-risk mental state, first episode psychosis and persistent schizophrenia
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Published:2024-07-30
Issue:1
Volume:14
Page:
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ISSN:2045-2322
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Container-title:Scientific Reports
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language:en
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Short-container-title:Sci Rep
Author:
Griffin J. D., Diederen K. M. J., Haarsma J., Jarratt Barnham I. C., Cook B. R. H., Fernandez-Egea E., Williamson S., van Sprang E. D., Gaillard R., Vinckier F., Goodyer I. M.ORCID, Bullmore Edward, Dolan Raymond, Goodyer Ian, Fonagy Peter, Jones Peter, Chamberlain Samuel, Moutoussis Michael, Hauser Tobias, Neufeld Sharon, Romero-Garcia Rafael, Clair Michelle St, Vértes Petra, Whitaker Kirstie, Inkster Becky, Prabhu Gita, Ooi Cinly, Toseeb Umar, Widmer Barry, Bhatti Junaid, Villis Laura, Alrumaithi Ayesha, Birt Sarah, Bowler Aislinn, Cleridou Kalia, Dadabhoy Hina, Davies Emma, Firkins Ashlyn, Granville Sian, Harding Elizabeth, Hopkins Alexandra, Isaacs Daniel, King Janchai, Kokorikou Danae, Maurice Christina, McIntosh Cleo, Memarzia Jessica, Mills Harriet, O’Donnell Ciara, Pantaleone Sara, Scott Jenny, Kiddle Beatrice, Polek Ela, Fearon Pasco, Suckling John, van Harmelen Anne-Laura, Kievit Rogier, Bethlehem Richard, Murray G. K.ORCID, Fletcher P. C.,
Abstract
AbstractWe used a probabilistic reversal learning task to examine prediction error-driven belief updating in three clinical groups with psychosis or psychosis-like symptoms. Study 1 compared people with at-risk mental state and first episode psychosis (FEP) to matched controls. Study 2 compared people diagnosed with treatment-resistant schizophrenia (TRS) to matched controls. The design replicated our previous work showing ketamine-related perturbations in how meta-level confidence maintained behavioural policy. We applied the same computational modelling analysis here, in order to compare the pharmacological model to three groups at different stages of psychosis. Accuracy was reduced in FEP, reflecting increased tendencies to shift strategy following probabilistic errors. The TRS group also showed a greater tendency to shift choice strategies though accuracy levels were not significantly reduced. Applying the previously-used computational modelling approach, we observed that only the TRS group showed altered confidence-based modulation of responding, previously observed under ketamine administration. Overall, our behavioural findings demonstrated resemblance between clinical groups (FEP and TRS) and ketamine in terms of a reduction in stabilisation of responding in a noisy environment. The computational analysis suggested that TRS, but not FEP, replicates ketamine effects but we consider the computational findings preliminary given limitations in performance of the model.
Publisher
Springer Science and Business Media LLC
Reference61 articles.
1. Miller, R. Schizophrenic psychology, associative learning and the role of forebrain dopamine. Med. Hypotheses 2, 203–211 (1976). 2. Gray, J. A., Feldon, J., Rawlins, J. N. P., Hemsley, D. & Smith, A. D. The neuropsychology of schizophrenia. Behav. Brain Sci. 14, 1–84 (1991). 3. Frith, C. The neural basis of hallucinations and delusions. Comptes rendus biologies 328(2), 169–175 (2005). 4. Fletcher, P. C. & Frith, C. D. Perceiving is believing: A Bayesian approach to explaining the positive symptoms of schizophrenia. Nat. Rev. Neurosci. 10(1), 48–58 (2009). 5. Adams, R. A., Stephan, K. E., Brown, H. R., Frith, C. D. & Friston, K. J. The computational anatomy of psychosis. Front. Psychiatry 4, 47 (2013).
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