Brain-Wide Analysis of Functional Connectivity in First-Episode and Chronic Stages of Schizophrenia

Tao Li(Sichuan University), Qiang Wang(Sichuan University), Jie Zhang(Fudan University), Edmund T. Rolls(University of Warwick), Wei Yang, Lena Palaniyappan(University of Nottingham), Lu Zhang, Wei Cheng(Fudan University), Ye Yao(Fudan University), Zhaowen Liu(Central South University), Xiaohong Gong(Fudan University), Qiang Luo(Fudan University), Yanqing Tang(First Hospital of China Medical University), Timothy J. Crow(Warneford Hospital), Matthew R. Broome(Oxford Health NHS Foundation Trust), Ke Xu(First Hospital of China Medical University), Chunbo Li(Shanghai Jiao Tong University), Jijun Wang(Shanghai Jiao Tong University), Zhening Liu(Central South University), Guangming Lu(Nanjing General Hospital of Nanjing Military Command), Fei Wang(First Hospital of China Medical University), Jianfeng Feng(Fudan University)
Schizophrenia Bulletin
July 21, 2016
Cited by 233Open Access
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Abstract

Published reports of functional abnormalities in schizophrenia remain divergent due to lack of staging point-of-view and whole-brain analysis. To identify key functional-connectivity differences of first-episode (FE) and chronic patients from controls using resting-state functional MRI, and determine changes that are specifically associated with disease onset, a clinical staging model is adopted. We analyze functional-connectivity differences in prodromal, FE (mostly drug naïve), and chronic patients from their matched controls from 6 independent datasets involving a total of 789 participants (343 patients). Brain-wide functional-connectivity analysis was performed in different datasets and the results from the datasets of the same stage were then integrated by meta-analysis, with Bonferroni correction for multiple comparisons. Prodromal patients differed from controls in their pattern of functional-connectivity involving the inferior frontal gyri (Broca's area). In FE patients, 90% of the functional-connectivity changes involved the frontal lobes, mostly the inferior frontal gyrus including Broca's area, and these changes were correlated with delusions/blunted affect. For chronic patients, functional-connectivity differences extended to wider areas of the brain, including reduced thalamo-frontal connectivity, and increased thalamo-temporal and thalamo-sensorimoter connectivity that were correlated with the positive, negative, and general symptoms, respectively. Thalamic changes became prominent at the chronic stage. These results provide evidence for distinct patterns of functional-dysconnectivity across FE and chronic stages of schizophrenia. Importantly, abnormalities in the frontal language networks appear early, at the time of disease onset. The identification of stage-specific pathological processes may help to understand the disease course of schizophrenia and identify neurobiological markers crucial for early diagnosis.


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