Cross‐cohort replicable resting‐state functional connectivity in predicting symptoms and cognition of schizophrenia

Author:

Zhao Chunzhi12,Jiang Rongtao3,Bustillo Juan4,Kochunov Peter5,Turner Jessica A.6,Liang Chuang12,Fu Zening6ORCID,Zhang Daoqiang12,Qi Shile12,Calhoun Vince D.6

Affiliation:

1. College of Computer Science and Technology Nanjing University of Aeronautics and Astronautics Nanjing China

2. Key Laboratory of Brain‐Machine Intelligence Technology, Ministry of Education Nanjing University of Aeronautics and Astronautics Nanjing China

3. Department of Radiology and Biomedical Imaging Yale School of Medicine New Haven Connecticut USA

4. Department of Psychiatry and Behavioral Sciences University of New Mexico Albuquerque New Mexico USA

5. Department of Psychiatry and Behavioral Sciences University of Texas Health Science Center Houston Houston Texas USA

6. Tri‐institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS) Georgia State University, Georgia Institute of Technology, Emory University Atlanta Georgia USA

Abstract

AbstractSchizophrenia (SZ) is a debilitating mental illness characterized by adolescence or early adulthood onset of psychosis, positive and negative symptoms, as well as cognitive impairments. Despite a plethora of studies leveraging functional connectivity (FC) from functional magnetic resonance imaging (fMRI) to predict symptoms and cognitive impairments of SZ, the findings have exhibited great heterogeneity. We aimed to identify congruous and replicable connectivity patterns capable of predicting positive and negative symptoms as well as cognitive impairments in SZ. Predictable functional connections (FCs) were identified by employing an individualized prediction model, whose replicability was further evaluated across three independent cohorts (BSNIP, SZ = 174; COBRE, SZ = 100; FBIRN, SZ = 161). Across cohorts, we observed that altered FCs in frontal‐temporal‐cingulate‐thalamic network were replicable in prediction of positive symptoms, while sensorimotor network was predictive of negative symptoms. Temporal‐parahippocampal network was consistently identified to be associated with reduced cognitive function. These replicable 23 FCs effectively distinguished SZ from healthy controls (HC) across three cohorts (82.7%, 90.2%, and 86.1%). Furthermore, models built using these replicable FCs showed comparable accuracies to those built using the whole‐brain features in predicting symptoms/cognition of SZ across the three cohorts (r = .17–.33, p < .05). Overall, our findings provide new insights into the neural underpinnings of SZ symptoms/cognition and offer potential targets for further research and possible clinical interventions.

Funder

Jiangsu Provincial Key Research and Development Program

National Institutes of Health

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Wiley

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