Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis

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作者
Kazusa Miyahara
Mizuki Hino
Risa Shishido
Atsuko Nagaoka
Ryuta Izumi
Hideki Hayashi
Akiyoshi Kakita
Hirooki Yabe
Hiroaki Tomita
Yasuto Kunii
机构
[1] Tohoku University,Department of Disaster Psychiatry, International Research Institute of Disaster Science
[2] Fukushima Medical University,Department of Neuropsychiatry, School of Medicine
[3] Niigata University,Department of Pathology, Brain Research Institute
[4] Tohoku University Hospital,Department of Psychiatry
[5] Tohoku University,Department of Psychiatry, Graduate School of Medicine
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Translational Psychiatry | / 13卷
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摘要
Schizophrenia is a multifactorial disorder, the genetic architecture of which remains unclear. Although many studies have examined the etiology of schizophrenia, the gene sets that contribute to its symptoms have not been fully investigated. In this study, we aimed to identify each gene set associated with corresponding symptoms of schizophrenia using the postmortem brains of 26 patients with schizophrenia and 51 controls. We classified genes expressed in the prefrontal cortex (analyzed by RNA-seq) into several modules by weighted gene co-expression network analysis (WGCNA) and examined the correlation between module expression and clinical characteristics. In addition, we calculated the polygenic risk score (PRS) for schizophrenia from Japanese genome-wide association studies, and investigated the association between the identified gene modules and PRS to evaluate whether genetic background affected gene expression. Finally, we conducted pathway analysis and upstream analysis using Ingenuity Pathway Analysis to clarify the functions and upstream regulators of symptom-related gene modules. As a result, three gene modules generated by WGCNA were significantly correlated with clinical characteristics, and one of these showed a significant association with PRS. Genes belonging to the transcriptional module associated with PRS significantly overlapped with signaling pathways of multiple sclerosis, neuroinflammation, and opioid use, suggesting that these pathways may also be profoundly implicated in schizophrenia. Upstream analysis indicated that genes in the detected module were profoundly regulated by lipopolysaccharides and CREB. This study identified schizophrenia symptom-related gene sets and their upstream regulators, revealing aspects of the pathophysiology of schizophrenia and identifying potential therapeutic targets.
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