Abstract

Current diagnostic criteria for schizophrenia place emphasis on delusions and hallucinations, whereas the classical descriptions of schizophrenia by Kraepelin and Bleuler emphasized disorganization and impoverishment of mental activity. Despite the availability of antipsychotic medication for treating delusions and hallucinations, many patients continue to experience persisting disability. Improving treatment requires a better understanding of the processes leading to persisting disability. We recently introduced the term classical schizophrenia to describe cases with disorganized and impoverished mental activity, cognitive impairment and predisposition to persisting disability. Recent evidence reveals that a polygenic score indicating risk for schizophrenia predicts severity of the features of classical schizophrenia: disorganization, and to a lesser extent, impoverishment of mental activity and cognitive impairment. Current understanding of brain function attributes a cardinal role to predictive coding: the process of generating models of the world that are successively updated in light of confirmation or contradiction by subsequent sensory information. It has been proposed that abnormalities of these predictive processes account for delusions and hallucinations. Here we examine the evidence provided by electrophysiology and fMRI indicating that imprecise predictive coding is the core pathological process in classical schizophrenia, accounting for disorganization, psychomotor poverty and cognitive impairment. Functional imaging reveals aberrant brain activity at network hubs engaged during encoding of predictions. We discuss the possibility that frequent prediction errors might promote excess release of the neurotransmitter, dopamine, thereby accounting for the occurrence of episodes of florid psychotic symptoms including delusions and hallucinations in classical schizophrenia. While the predictive coding hypotheses partially accounts for the time-course of classical schizophrenia, the overall body of evidence indicates that environmental factors also contribute. We discuss the evidence that chronic inflammation is a mechanism that might link diverse genetic and environmental etiological factors, and contribute to the proposed imprecision of predictive coding.

Highlights

  • Our hypothesis is similar to the proposal of Adams et al (2013) that trait abnormalities might arise from a decrease in the precision of internally generated predictions, but we propose that this “trait” reflects the “core” process in the pathway to classical schizophrenia: persistently imprecise predictions generate percepts that are both salient and tangential, reflected in disorganization symptoms, while a steady stream of minor error signals elevate net background dopamine levels and increase the risk of acute psychosis

  • In accord with the observation that the genetic variants expressed in glutamatergic and GABAergic neurons contribute to the polygenic risk score for schizophrenia associated with the clinical features of classical schizophrenia (Legge et al, 2021), taken together with the proposal by Adams et al (2013) that reduced synaptic gain arising from abnormality of glutamatergic or GABAergic transmission might play a cardinal role in trait abnormalities, we propose that classical schizophrenia arises from imprecise priors resulting from reduced synaptic gain in pyramidal neurons

  • In accord with our overarching goal of understanding of the processes that lead to poor functional outcome in schizophrenia, we have identified a specific clinical profile that we have designated “classical schizophrenia.”

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Summary

INTRODUCTION

In the combined structural and functional imaging study comparing schizophrenia with bipolar disorder discussed in the section entitled Perceptual Organization, Palaniyappan and Liddle (2014) confirmed that in the contrast of patients with schizophrenia with healthy controls, the patients exhibited diminished gyrification in left insula, left superior frontal gyrus, regions in the vicinity of the tempo-parietal junction bilaterally, and left precuneus and posterior cingulate. They conducted a conjunction analysis to identify brain regions exhibiting both diminished gyrification and increased functional connectivity in patients with schizophrenia relative to patients with bipolar disorder. Investigation of the relationships between markers of inflammation and electrophysiological markers indicative of imprecise predictive coding, such as MMN and PMBR in schizophrenia is warranted

DISCUSSION
Findings
DATA AVAILABILITY STATEMENT
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