Literature DB >> 26341902

Theory of mind network activity is altered in subjects with familial liability for schizophrenia.

Sebastian Mohnke1, Susanne Erk2, Knut Schnell3, Nina Romanczuk-Seiferth2, Phöbe Schmierer2, Lydia Romund2, Maria Garbusow2, Carolin Wackerhagen2, Stephan Ripke4, Oliver Grimm5, Leila Haller6, Stephanie H Witt7, Franziska Degenhardt8, Heike Tost6, Andreas Heinz2, Andreas Meyer-Lindenberg6, Henrik Walter2.   

Abstract

As evidenced by a multitude of studies, abnormalities in Theory of Mind (ToM) and its neural processing might constitute an intermediate phenotype of schizophrenia. If so, neural alterations during ToM should be observable in unaffected relatives of patients as well, since they share a considerable amount of genetic risk. While behaviorally, impaired ToM function is confirmed meta-analytically in relatives, evidence on aberrant function of the neural ToM network is sparse and inconclusive. The present study therefore aimed to further explore the neural correlates of ToM in relatives of schizophrenia. About 297 controls and 63 unaffected first-degree relatives of patients with schizophrenia performed a ToM task during functional magnetic resonance imaging. Consistent with the literature relatives exhibited decreased activity of the medial prefrontal cortex. Additionally, increased recruitment of the right middle temporal gyrus and posterior cingulate cortex was found, which was related to subclinical paranoid symptoms in relatives. These results further support decreased medial prefrontal activation during ToM as an intermediate phenotype of genetic risk for schizophrenia. Enhanced recruitment of posterior ToM areas in relatives might indicate inefficiency mechanisms in the presence of genetic risk.
© The Author (2015). Published by Oxford University Press. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  imaging genetics; intermediate phenotype; medial prefrontal cortex; mentalizing; psychosis

Mesh:

Year:  2015        PMID: 26341902      PMCID: PMC4733339          DOI: 10.1093/scan/nsv111

Source DB:  PubMed          Journal:  Soc Cogn Affect Neurosci        ISSN: 1749-5016            Impact factor:   3.436


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