Atypical processing of uncertainty in individuals at risk for psychosis.

Neuroimage Clin

Translational Neuromodeling Unit (TNU), Institute for Biomedical Engineering, University of Zurich and Swiss Federal Institute of Technology (ETH) Zurich, Zurich, Switzerland; Max Planck Institute for Metabolism Research, Cologne, Germany; Wellcome Centre for Human Neuroimaging, University College London, London, United Kingdom.

Published: February 2021

AI Article Synopsis

  • Current theories suggest that abnormalities in learning signals, especially in prediction errors (PEs) and uncertainty, play a key role in the development of delusional beliefs in psychosis.
  • A study using fMRI and computational behavior analysis found that clinical high-risk (CHR) individuals exhibit higher volatility estimates compared to control participants during a probabilistic learning task.
  • Results indicated that while CHR individuals showed increased activity in certain brain regions in response to low-level PEs, they had reduced activation associated with higher-level PEs, implying a complex learning abnormality that may contribute to a predisposition for delusion formation.

Article Abstract

Current theories of psychosis highlight the role of abnormal learning signals, i.e., prediction errors (PEs) and uncertainty, in the formation of delusional beliefs. We employed computational analyses of behaviour and functional magnetic resonance imaging (fMRI) to examine whether such abnormalities are evident in clinical high risk (CHR) individuals. Non-medicated CHR individuals (n = 13) and control participants (n = 13) performed a probabilistic learning paradigm during fMRI data acquisition. We used a hierarchical Bayesian model to infer subject-specific computations from behaviour - with a focus on PEs and uncertainty (or its inverse, precision) at different levels, including environmental 'volatility' - and used these computational quantities for analyses of fMRI data. Computational modelling of CHR individuals' behaviour indicated volatility estimates converged to significantly higher levels than in controls. Model-based fMRI demonstrated increased activity in prefrontal and insular regions of CHR individuals in response to precision-weighted low-level outcome PEs, while activations of prefrontal, orbitofrontal and anterior insula cortex by higher-level PEs (that serve to update volatility estimates) were reduced. Additionally, prefrontal cortical activity in response to outcome PEs in CHR was negatively associated with clinical measures of global functioning. Our results suggest a multi-faceted learning abnormality in CHR individuals under conditions of environmental uncertainty, comprising higher levels of volatility estimates combined with reduced cortical activation, and abnormally high activations in prefrontal and insular areas by precision-weighted outcome PEs. This atypical representation of high- and low-level learning signals might reflect a predisposition to delusion formation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076146PMC
http://dx.doi.org/10.1016/j.nicl.2020.102239DOI Listing

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