Neuroimmune transcriptome changes in patient brains of psychiatric and neurological disorders

转录组 精神分裂症(面向对象编程) 神经炎症 双相情感障碍 微阵列 免疫系统 神经科学 重性抑郁障碍 疾病 生物 基因 基因表达 医学 精神科 免疫学 遗传学 内科学 扁桃形结构 认知
作者
Yu Chen,Rujia Dai,Longfei Tang,Tatiana Mikhailova,Qiuman Liang,Miao Li,Jiaqi Zhou,Richard F. Kopp,Cynthia Shannon Weickert,Chao Chen,Chunyu Liu
出处
期刊:Molecular Psychiatry [Springer Nature]
卷期号:28 (2): 710-721 被引量:26
标识
DOI:10.1038/s41380-022-01854-7
摘要

Neuroinflammation has been implicated in multiple brain disorders but the extent and the magnitude of change in immune-related genes (IRGs) across distinct brain disorders has not been directly compared. In this study, 1275 IRGs were curated and their expression changes investigated in 2467 postmortem brains of controls and patients with six major brain disorders, including schizophrenia (SCZ), bipolar disorder (BD), autism spectrum disorder (ASD), major depressive disorder (MDD), Alzheimer’s disease (AD), and Parkinson’s disease (PD). There were 865 IRGs present across all microarray and RNA-seq datasets. More than 60% of the IRGs had significantly altered expression in at least one of the six disorders. The differentially expressed immune-related genes (dIRGs) shared across disorders were mainly related to innate immunity. Moreover, sex, tissue, and putative cell type were systematically evaluated for immune alterations in different neuropsychiatric disorders. Co-expression networks revealed that transcripts of the neuroimmune systems interacted with neuronal-systems, both of which contribute to the pathology of brain disorders. However, only a few genes with expression changes were also identified as containing risk variants in genome-wide association studies. The transcriptome alterations at gene and network levels may clarify the immune-related pathophysiology and help to better define neuropsychiatric and neurological disorders.
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