Genome-wide analysis of DNA methylation in 106 schizophrenia family trios in Han Chinese

• DOI: 10.1016/j.ebiom.2021.103609
• Publication Date: 2021-10-09T16:51:23Z
• Authors: Lu Shen; Xiaoying Lv; Hailiang Huang; Mo Li; Cong Huai; Xi Wu; Hao Wu; Jingsong Ma; Luan Chen; Ting Wang; Jie Tan; Yidan Sun; Lixing Li; Yi Shi; Chao Yang; Lei Cai; Yana Lu; Yan Zhang; Saizheng Weng; Shaobin Tai; Na Zhang; Lin He; Chunling Wan; Shengying Qin
• Keywords: Cerebral Cortex; 0301 basic medicine; Medicine (General); Chinese; Research paper; Receptors, Notch; Trios; R; DNA Methylation; 3. Good health; 03 medical and health sciences; R5-920; Asian People; Databases, Genetic; Schizophrenia; Medicine; Humans; CpG Islands; Genetic Predisposition to Disease; Mitogen-Activated Protein Kinases; Wnt Signaling Pathway; Biomarkers; Genome-Wide Association Study

Schizophrenia (SCZ) is a severe psychiatric disorder that affects approximately 0.75% of the global population. Both genetic and environmental factors contribute to development of SCZ. SCZ tends to run in family while both genetic and environmental factor contribute to its etiology. Much evidence suggested that alterations in DNA methylations occurred in SCZ patients.To investigate potential inheritable pattern of DNA methylation in SCZ family, we performed a genome-wide analysis of DNA methylation of peripheral blood samples from 106 Chinese SCZ family trios. Genome-wide DNA methylations were quantified by Agilent 1 × 244 k Human Methylation Microarray.In this study, we proposed a loci inheritance frequency model that allows characterization of differential methylated regions as SCZ biomarkers. Based on this model, 112 hypermethylated and 125 hypomethylated regions were identified. Additionally, 121 hypermethylated and 139 hypomethylated genes were annotated. The results of functional enrichment analysis indicated that multiple differentially methylated genes (DMGs) involved in Notch/HH/Wnt signaling, MAPK signaling, GPCR signaling, immune response signaling. Notably, a number of hypomethylated genes were significantly enriched in cerebral cortex and functionally enriched in nervous system development.Our findings not only validated previously discovered risk genes of SCZ but also identified novel candidate DMGs in SCZ. These results may further the understanding of altered DNA methylations in SCZ.None.