The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Olszewski, Amy; Kikinis, Zora; Gonzalez, Christie; Coman, Ioana; Makris, Nikolaos; Gong, Xue; Rathi, Yogesh; Zhu, Anni; Antshel, Kevin; Fremont, Wanda; Kubicki, Marek; Bouix, Sylvain; Shenton, Martha; Kates, Wendy
• Is Part Of: Behavioral and brain functions. Volume 13:Issue 1(2017)
• Page Start: 1
• Page End: 17
• Publication Date: 2017-12
• Subjects: 22q11.2 deletion syndrome -- Social brain network -- Social cognition -- Two-tensor tractography -- White matter tracts; Neurobiology -- Periodicals; Cognitive neuroscience -- Periodicals; Neurophysiology -- Periodicals; Neuropsychology -- Periodicals; Brain -- Localization of functions -- Periodicals; Human behavior -- Periodicals; Animal behavior -- Periodicals; 612.8205
• DOI: 10.1186/s12993-017-0122-7
• Languages: English
• ISSNs: 1744-9081

Abstract

Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is associated with a 25-fold increase in schizophrenia. Both individuals with 22q11.2DS and those with schizophrenia present with social cognitive deficits, which are putatively subserved by a network of brain regions that are involved in the processing of social cognitive information. This study used two-tensor tractography to examine the white matter tracts believed to underlie the social brain network in a group of 57 young adults with 22q11.2DS compared to 30 unaffected controls. Results Results indicated that relative to controls, participants with 22q11.2DS showed significant differences in several DTI metrics within the inferior fronto-occipital fasciculus, cingulum bundle, thalamo-frontal tract, and inferior longitudinal fasciculus. In addition, participants with 22q11.2DS showed significant differences in scores on measures of social cognition, including the Social Responsiveness Scale and Trait Emotional Intelligence Questionnaire. Further analyses among individuals with 22q11.2DS demonstrated an association between DTI metrics and positive and negative symptoms of psychosis, as well as differentiation between individuals with 22q11.2DS and overt psychosis, relative to those with positive prodromal symptoms or no psychosis. Conclusions Findings suggest that white matter disruption, specifically disrupted axonal coherence in the right inferior fronto-occipital fasciculus, may be a biomarker for social cognitive difficulties and psychosis in individuals with 22q11.2DS.