Intrinsic Connectivity Network-Based Classification and Detection of Psychotic Symptoms in Youth With 22q11.2 Deletions

• Published in: Cerebral cortex (New York, N.Y. 1991) N.Y. 1991), 2017-06, Vol.27 (6), p.3294-3306
• Main Authors: Schreiner, Matthew, Forsyth, Jennifer K, Karlsgodt, Katherine H, Anderson, Ariana E, Hirsh, Nurit, Kushan, Leila, Uddin, Lucina Q, Mattiacio, Leah, Coman, Ioana L, Kates, Wendy R, Bearden, Carrie E
• Format: Article
• Language: English
• Subjects: Adolescent; Case-Control Studies; Child; Cohort Studies; Connectome; DiGeorge Syndrome - complications; Female; Gyrus Cinguli - diagnostic imaging; Gyrus Cinguli - physiopathology; Humans; Magnetic Resonance Imaging; Male; Motion; Nerve Net - diagnostic imaging; Nerve Net - physiopathology; Neuropsychological Tests; Original; Oxygen - blood; Parietal Lobe - diagnostic imaging; Parietal Lobe - physiopathology; Psychiatric Status Rating Scales; Psychotic Disorders - classification; Psychotic Disorders - etiology; Psychotic Disorders - genetics; Psychotic Disorders - pathology; Young Adult
• ISSN: 1047-3211; 1460-2199
• DOI: 10.1093/cercor/bhx076

22q11.2 Deletion syndrome (22q11DS) is a genetic disorder associated with numerous phenotypic consequences and is one of the greatest known risk factors for psychosis. We investigated intrinsic-connectivity-networks (ICNs) as potential biomarkers for patient and psychosis-risk status in 2 independent cohorts, UCLA (33 22q11DS-participants, 33 demographically matched controls), and Syracuse (28 22q11DS, 28 controls). After assessing group connectivity differences, ICNs from the UCLA cohort were used to train classifiers to distinguish cases from controls, and to predict psychosis risk status within 22q11DS; classifiers were subsequently tested on the Syracuse cohort. In both cohorts we observed significant hypoconnectivity in 22q11DS relative to controls within anterior cingulate (ACC)/precuneus, executive, default mode (DMN), posterior DMN, and salience networks. Of 12 ICN-derived classifiers tested in the Syracuse replication-cohort, the ACC/precuneus, DMN, and posterior DMN classifiers accurately distinguished between 22q11DS and controls. Within 22q11DS subjects, connectivity alterations within 4 networks predicted psychosis risk status for a given individual in both cohorts: the ACC/precuneus, DMN, left executive, and salience networks. Widespread within-network-hypoconnectivity in large-scale networks implicated in higher-order cognition may be a defining characteristic of 22q11DS during adolescence and early adulthood; furthermore, loss of coherence within these networks may be a valuable biomarker for individual prediction of psychosis-risk in 22q11DS.