Stronger Top-Down and Weaker Bottom-Up Frontotemporal Connections During Sensory Learning Are Associated With Severity of Psychotic Phenomena
Ilvana Dzafic, Kit Melissa Larsen, Hayley Darke, Holly Pertile, Olivia Carter, Suresh Sundram, Marta I. Garrido
Schizophrenia Bulletin December 7, 2020 DOI: 10.1093/schbul/sbaa188 via OpenAlex
Summary
AI-generated from the abstractPeople with schizophrenia have reduced neural prediction-error signals (mismatch negativity in stable contexts, P300 in volatile contexts) that are specific to the schizophrenia spectrum, whereas altered brain connectivity—decreased intrinsic connectivity in the left primary auditory cortex and right inferior frontal gyrus (IFG), reduced bottom-up and increased top-down frontotemporal connectivity—occurs across all participants as psychotic experiences intensify. Impaired sensory learning behavior was linked to lower intrinsic connectivity in the IFG, which also decreased with greater severity of psychotic experiences. The findings suggest that distinct neural mechanisms underlie schizophrenia-specific deficits versus general psychosis-related connectivity changes.
Study at a glance
| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Sample size | 66 |
| Population | 22 schizophrenia spectrum inpatients, 22 nonpsychotic inpatients, and 22 nonclinical controls |
| Keywords | Mismatch negativity Psychosis Neuroscience Delusion Schizophrenia object-oriented programming |
| Citations | 26 |
| Key finding | Reduced prediction errors are specific to the schizophrenia spectrum, while deficits in brain connectivity are aligned on the psychosis continuum. |
Abstract
Recent theories in computational psychiatry propose that unusual perceptual experiences and delusional beliefs may emerge as a consequence of aberrant inference and disruptions in sensory learning. The current study investigates these theories and examines the alterations that are specific to schizophrenia spectrum disorders vs those that occur as psychotic phenomena intensify, regardless of diagnosis. We recruited 66 participants: 22 schizophrenia spectrum inpatients, 22 nonpsychotic inpatients, and 22 nonclinical controls. Participants completed the reversal oddball task with volatility manipulated. We recorded neural responses with electroencephalography and measured behavioral errors to inferences on sound probabilities. Furthermore, we explored neural dynamics using dynamic causal modeling (DCM). Attenuated prediction errors (PEs) were specifically observed in the schizophrenia spectrum, with reductions in mismatch negativity in stable, and P300 in volatile, contexts. Conversely, aberrations in connectivity were observed across all participants as psychotic phenomena increased. DCM revealed that impaired sensory learning behavior was associated with decreased intrinsic connectivity in the left primary auditory cortex and right inferior frontal gyrus (IFG); connectivity in the latter was also reduced with greater severity of psychotic experiences. Moreover, people who experienced more hallucinations and psychotic-like symptoms had decreased bottom-up and increased top-down frontotemporal connectivity, respectively. The findings provide evidence that reduced PEs are specific to the schizophrenia spectrum, but deficits in brain connectivity are aligned on the psychosis continuum. Along the continuum, psychotic experiences were related to an aberrant interplay between top-down, bottom-up, and intrinsic connectivity in the IFG during sensory uncertainty. These findings provide novel insights into psychosis neurocomputational pathophysiology.