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Dopaminergic basis for signaling belief updates, but not surprise, and the link to paranoia

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TLDR
It is demonstrated that dopamine is strongly related to neural signals encoding belief updates, and that belief updating itself is closely related to the expression of individual differences in paranoid ideation.
Abstract
Distinguishing between meaningful and meaningless sensory information is fundamental to forming accurate representations of the world. Dopamine is thought to play a central role in processing the meaningful information content of observations, which motivates an agent to update their beliefs about the environment. However, direct evidence for dopamine’s role in human belief updating is lacking. We addressed this question in healthy volunteers who performed a model-based fMRI task designed to separate the neural processing of meaningful and meaningless sensory information. We modeled participant behavior using a normative Bayesian observer model and used the magnitude of the model-derived belief update following an observation to quantify its meaningful information content. We also acquired PET imaging measures of dopamine function in the same subjects. We show that the magnitude of belief updates about task structure (meaningful information), but not pure sensory surprise (meaningless information), are encoded in midbrain and ventral striatum activity. Using PET we show that the neural encoding of meaningful information is negatively related to dopamine-2/3 receptor availability in the midbrain and dexamphetamine-induced dopamine release capacity in the striatum. Trial-by-trial analysis of task performance indicated that subclinical paranoid ideation is negatively related to behavioral sensitivity to observations carrying meaningful information about the task structure. The findings provide direct evidence implicating dopamine in model-based belief updating in humans and have implications for understating the pathophysiology of psychotic disorders where dopamine function is disrupted.

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Citations
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Schizophrenia-An Overview

TL;DR: An overview of the clinical characteristics, epidemiology, genetics, neuroscience, and psychopharmacology of schizophrenia is provided to provide a basis to understand the disorder and its treatment.
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Schizophrenia, Dopamine and the Striatum: From Biology to Symptoms

TL;DR: This Review draws together developments in neuroimaging techniques that led to the unanticipated finding that dopaminergic dysfunction in schizophrenia is greatest within nigrostriatal pathways, implicating the dorsal striatum in the pathophysiology and calling into question the mesolimbic theory.
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Dopamine and glutamate in schizophrenia: biology, symptoms and treatment

TL;DR: Converging evidence indicates that genetic and environmental risk factors for schizophrenia underlie disruption of glutamatergic and dopaminergic function, however, while genetic influences may directly underlie glutamatorgic dysfunction, few genetic risk variants directly implicate the dopamine system, indicating that aberrant dopamine signalling is likely to be predominantly due to other factors.
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Computational mechanisms of curiosity and goal-directed exploration.

TL;DR: It is shown how different types of information-gain emerge when casting behaviour as surprise minimisation, termed active inference and active learning, and how these forms of exploration induce distinct patterns of ‘Bayes-optimal’ behaviour.
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The Misestimation of Uncertainty in Affective Disorders.

TL;DR: The logic behind this process is explained and the evidence that human learners use estimates of uncertainty to sculpt their learning is described, suggesting that misestimation of uncertainty is involved in the development of anxiety and depression.
References
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A Neural Substrate of Prediction and Reward

TL;DR: Findings in this work indicate that dopaminergic neurons in the primate whose fluctuating output apparently signals changes or errors in the predictions of future salient and rewarding events can be understood through quantitative theories of adaptive optimizing control.
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Cluster failure: Why fMRI inferences for spatial extent have inflated false-positive rates

TL;DR: It is found that the most common software packages for fMRI analysis (SPM, FSL, AFNI) can result in false-positive rates of up to 70%.
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Psychosis as a state of aberrant salience: A framework linking biology, phenomenology, and pharmacology in schizophrenia.

TL;DR: A heuristic framework for linking the psychological and biological in psychosis is provided and it is proposed that a dysregulated, hyperdopaminergic state, at a "brain" level of description and analysis, leads to an aberrant assignment of salience to the elements of one's experience, at an "mind" level.
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Simplified Reference Tissue Model for PET Receptor Studies

TL;DR: The reference tissue model allows for quantification of receptor kinetics without measuring the arterial input function, thus avoiding arterial cannulation and time-consuming metabolite measurements, and for the ligands tested the three-parameter model is a better choice, combining increased convergence rate with increased stability.
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Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: a hypothesis for the etiology of schizophrenia

TL;DR: In this paper, a novel mechanism for regulating dopamine activity in subcortical sites and its possible relevance to schizophrenia is proposed, which is based on the regulation of dopamine release into sub cortical regions occurring via two independent mechanisms: (1) transient or phasic dopamine release caused by dopamine neuron firing, and (2) sustained, "background" tonic release regulated by prefrontal cortical afferents.
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