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The neural correlates of the visual consciousness in schizophrenia: an fMRI study

Stéphanie Lefebvre, É. Very, Renaud Jardri, Mathilde Horn, Antoine Yrondi, Christine Delmaire, C. Rascle, K. Dujardin, Pierre Thomas, D. Pins

European Archives of Psychiatry and Clinical Neuroscience August 19, 2020 DOI: 10.1007/s00406-020-01167-2 via Semantic Scholar

Summary

AI-generated from the abstract

People with schizophrenia have a higher visual detection threshold than healthy controls, meaning they need stronger visual input to become consciously aware of it. Brain imaging showed that during conscious vision, patients failed to activate occipital areas as strongly as controls; during unconscious vision, they failed to activate a widespread network; and during the moment of becoming conscious of a visual stimulus, they failed to activate the anterior cingulate cortex.

Study at a glance

Characteristics Cross-sectional, case-control Peer reviewed
Sample size 34
Population Healthy participants and patients with schizophrenia
Keywords Medicine Psychology
Key finding Consciousness disorders in schizophrenia involve distinct brain dysfunctions at different stages of consciousness, with impaired activation of occipital areas during conscious vision, a widespread network during unconscious vision, and the anterior cingulate cortex during conscious access.

Abstract

In the current literature, two distinct and opposite models are suggested to explain the consciousness disorders in schizophrenia. The first one suggests that consciousness disorders rely on a low-level processing deficit, when the second model suggests that consciousness disorders rely on disruption in the ability to consciously access information, with preserved unconscious processing. The current study aims to understand the mechanisms associated with visual consciousness disorder in order to pave the road that will settle the debate regarding these hypotheses. During a functional magnetic resonance imaging session, 19 healthy participants (HC) and 15 patients with schizophrenia (SCZ) performed a visual detection task to compare the neural substrates associated with the conscious access to the visual inputs. The visual detection threshold was significantly higher in SCZ than in HC [t(32) = 3.37, p = 0.002]. Whole-brain ANOVA demonstrated that around the visual detection threshold patients with SCZ failed to activate a large network of brain areas compared to HC. (1) During conscious vision, HC engaged more the left cuneus and the right occipital cortex than patients with SCZ, (2) during unconscious vision, HC engaged a large network that patients with SCZ failed to activate, and finally, (3) during the access to consciousness process, patients with SCZ failed to activate the anterior cingulate cortex. These results suggest that the consciousness disorders in schizophrenia rely on specific dysfunctions depending on the consciousness stage. The disorders of the conscious vision are associated with dysfunction of occipital areas while the ones associated with unconscious vision rely on a large widespread network. Finally, the conscious access to the visual inputs is impaired by a dysfunction of the anterior cingulate cortex. The current study suggests that none of the two suggested models can explain consciousness disorders in schizophrenia. We suggest that there is an alternative model supporting that the conscious access to visual inputs is due to a disengagement of the supragenual anterior cingulate during the unconscious processing of the visual inputs associated with a sensory deficit.

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