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The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study
Amy K Olszewski1, Zora Kikinis2, Christie S Gonzalez3
1Department of Psychiatry, SUNY Upstate Medical University, 750 E. Adams St., Syracuse, NY, 13210, USA.
Behavioral and Brain Functions : BBF
|February 18, 2017
Summary
Individuals with 22q11.2 deletion syndrome (22q11.2DS) show disrupted white matter tracts, impacting social cognition and psychosis risk. Disrupted tracts, particularly in the right inferior fronto-occipital fasciculus, may serve as a biomarker.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder.
- 22q11.2DS is linked to a 25-fold increased risk of schizophrenia.
- Individuals with 22q11.2DS and schizophrenia exhibit social cognitive deficits.
Purpose of the Study:
- To investigate white matter tracts in the social brain network of individuals with 22q11.2DS.
- To compare white matter integrity between 22q11.2DS patients and healthy controls.
- To explore the relationship between white matter integrity, social cognition, and psychosis symptoms in 22q11.2DS.
Main Methods:
- Two-tensor tractography was employed to analyze white matter.
- Diffusion Tensor Imaging (DTI) metrics were assessed in specific white matter tracts.
- Social cognition was measured using the Social Responsiveness Scale and Trait Emotional Intelligence Questionnaire.
Main Results:
- Participants with 22q11.2DS showed significant differences in DTI metrics within key tracts, including the inferior fronto-occipital fasciculus.
- 22q11.2DS group exhibited impaired social cognition scores.
- DTI metrics correlated with psychosis symptoms, differentiating between overt psychosis and prodromal symptoms.
Conclusions:
- White matter disruption, especially in the right inferior fronto-occipital fasciculus, is implicated in 22q11.2DS.
- Disrupted axonal coherence may be a biomarker for social cognitive deficits in 22q11.2DS.
- These findings highlight potential neurobiological markers for psychosis risk in 22q11.2DS.
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