Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/95864
Title: | A Fundamental Distinction in Early Neural Processing of Implicit Social Interpretation in Schizophrenia and Bipolar Disorder | Authors: | Madeira, Nuno Martins, Ricardo Filipe Alves Valente Duarte, João Costa, Gabriel Nascimento Ferreira da Macedo, António Ferreira de Castelo Branco, Miguel de Sá e Sousa |
Issue Date: | Oct-2021 | Publisher: | Elsevier | metadata.degois.publication.title: | NeuroImage: Clinical | metadata.degois.publication.volume: | 32 | Abstract: | Background: Social cognition impairment is a key phenomenon in serious mental disorders such as schizophrenia (SCZ) and bipolar disorder (BPD). Although genetic and neurobiological studies have suggested common neural correlates, here we hypothesized that a fundamental dissociation of social processing occurs at an early level in these conditions. Methods: Based on the hypothesis that key structures in the social brain, namely the temporoparietal junction, should present distinctive features in SCZ and BPD during low-level social judgment, we conducted a case-control study in SCZ (n = 20) and BPD (n = 20) patients and controls (n = 20), using task-based fMRI during a Theory of Mind (ToM) visual paradigm leading to interpretation of social meaning based on simple geometric figures. Results: We found opposite neural responses in two core ToM regions: SCZ patients showed social content-related deactivation (relative to controls and BPD) of the right supramarginal gyrus, while the opposite pattern was found in BPD; reverse patterns, relative to controls and SCZ, were found in the left posterior superior temporal gyrus, a region involved in inferring other’s intentions. Receiver-operating-characteristic curve analysis showed 88% accuracy in discriminating the two clinical groups based on these neural responses. Conclusions: These contrasting activation patterns of the temporoparietal junction in SCZ and BPD represent mechanistic differences of social cognitive dysfunction that may be explored as biomarkers or therapeutic targets. | URI: | https://hdl.handle.net/10316/95864 | ISSN: | 22131582 | DOI: | 10.1016/j.nicl.2021.102836 | Rights: | openAccess |
Appears in Collections: | I&D CIBIT - Artigos em Revistas Internacionais |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
full-text.pdf | full-text | 3.31 MB | Adobe PDF | View/Open |
SCOPUSTM
Citations
5
checked on Oct 28, 2024
WEB OF SCIENCETM
Citations
5
checked on Oct 2, 2024
Page view(s)
303
checked on Oct 29, 2024
Download(s)
153
checked on Oct 29, 2024
Google ScholarTM
Check
Altmetric
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.