Abstract

Ongoing research suggests preliminary, though not entirely consistent, evidence of neural abnormalities in signalling prediction errors in schizophrenia. Supporting theories suggest mechanistic links between the disruption of these processes and the generation of psychotic symptoms. However, it is unknown at what stage in the pathogenesis of psychosis these impairments in prediction-error signalling develop. One major confound in prior studies is the use of medicated patients with strongly varying disease durations. Our study aims to investigate the involvement of the meso-cortico-striatal circuitry during reward prediction-error signalling in earliest stages of psychosis. We studied patients with first-episode psychosis (FEP) and help-seeking individuals at-risk for psychosis due to sub-threshold prodromal psychotic symptoms. Patients with either FEP (n = 14), or at-risk for developing psychosis (n = 30), and healthy volunteers (n = 39) performed a reinforcement learning task during fMRI scanning. ANOVA revealed significant (p < 0.05 family-wise error corrected) prediction-error signalling differences between groups in the dopaminergic midbrain and right middle frontal gyrus (dorsolateral prefrontal cortex, DLPFC). FEP patients showed disrupted reward prediction-error signalling compared to controls in both regions. At-risk patients showed intermediate activation in the midbrain that significantly differed from controls and from FEP patients, but DLPFC activation that did not differ from controls. Our study confirms that FEP patients have abnormal meso-cortical signalling of reward-prediction errors, whereas reward-prediction-error dysfunction in the at-risk patients appears to show a more nuanced pattern of activation with a degree of midbrain impairment but preserved cortical function.

Highlights

  • The cognitive basis of psychotic symptoms remains unknown, but abnormalities in the processing of prediction error have been proposed to contribute to the development of psychotic symptoms [1, 2]

  • In our planned group comparisons (Supplementary Table 1 and Supplementary Figure 3), we found that controls had a significantly higher probability for a win stay behaviour than first-episode psychosis (FEP) patients on reward and neutral trial types and marginally on bivalent trials (p = 0.062)

  • At-risk patients had a significantly higher probability of win stay behaviour in neutral trials compared to FEP (p = 0.013), but the two patient groups did not differ on the other trial types

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Summary

Introduction

The cognitive basis of psychotic symptoms remains unknown, but abnormalities in the processing of prediction error have been proposed to contribute to the development of psychotic symptoms [1, 2]. Our previous work in psychosis patients has identified mesocortico-striatal prediction-error deficits, involving midbrain, striatum and frontal cortex, especially right dorsolateral prefrontal cortex (DLPFC) [12, 14]. Meso-corticalstriatal regions, including the right DLPFC, are activated during associative learning in functional Magnetic Resonance Imaging (fMRI) studies, especially when expectations are violated, and the fMRI signal scales with prediction-error magnitude [16,17,18,19]. Work from our group and others has supported this view by showing differences in the right DLPFC between patients and controls [12, 18, 20] Dysfunction of these regions may manifest in abnormalities in learning and motivational salience [21,22,23], potentially contributing to the development of psychosis [24]. A major complication in the interpretation of patient studies is that several studies are potentially confounded by having either all, or the majority of patients, taking antipsychotic medication, which

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