Salience network-midbrain dysconnectivity and blunted reward signals in schizophrenia
Abstract
Theories of schizophrenia propose that abnormal functioning of the neural reward system is linked to negative and psychotic symptoms, by disruption of reward processing and promotion of context-independent false associations. Recently it has been argued that an insula-anterior cingulate cortex (ACC) salience network system enables switching of brain states from the default mode to a task-related activity mode. Abnormal interaction between the insula-ACC system and reward processing regions may help explain abnormal reinforcer processing and symptoms. Here we use fMRI to assess the neural correlates of reward processing in schizophrenia. Furthermore we investigated functional connectivity between the dopaminergic midbrain, a key region for the processing of reinforcers, and other brain regions. In response to rewards, controls activated task related regions (striatum, amygdala/hippocampus and midbrain) and the insula-ACC salience network. Patients similarly activated the insula-ACC salience network system but failed to activate task related regions. Reduced functional connectivity between the midbrain and the insula was found in schizophrenia, with the extent of this abnormality correlating with increased psychotic symptoms. The findings support the notion that reward processing is abnormal in schizophrenia and highlight the potential role of abnormal interactions between the insula-ACC salience network and reward regions.
Citation
Gradin , V , Waiter , G , O'Connor , A R , Romaniuk , L , Stickle , C , Matthews , K , Hall , J & Steele , D 2013 , ' Salience network-midbrain dysconnectivity and blunted reward signals in schizophrenia ' , Psychiatry Research: Neuroimaging , vol. 211 , no. 2 , pp. 104-111 . https://doi.org/10.1016/j.pscychresns.2012.06.003
Publication
Psychiatry Research: Neuroimaging
Status
Peer reviewed
ISSN
0925-4927Type
Journal article
Rights
This is an author version of this work. The published version (c) 2012 Elsevier Ireland Ltd is available from www.sciencedirect.com
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