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Integrating genome-wide association study and expression quantitative trait locus study identifies multiple genes and gene sets associated with schizophrenia

  • Yan Zhao
  • , Awen He
  • , Feng Zhu
  • , Miao Ding
  • , Jingcan Hao
  • , Qianrui Fan
  • , Ping Li
  • , Li Liu
  • , Yanan Du
  • , Xiao Liang
  • , Xiong Guo
  • , Feng Zhang
  • , Xiancang Ma
  • Xi'an Jiaotong University
  • The First Affiliated Hospital of Xi’an Jiaotong University

科研成果: 期刊稿件文章同行评审

29 引用 (Scopus)

摘要

Schizophrenia is a serious mental disease with high heritability. To better understand the genetic basis of schizophrenia, we conducted a large scale integrative analysis of genome-wide association study (GWAS) and expression quantitative trait loci (eQTLs) data. GWAS summary data was derived from a published GWAS of schizophrenia, containing 9394 schizophrenia patients and 12,462 healthy controls. The eQTLs dataset was obtained from an eQTLs meta-analysis of 5311 subjects, containing 923,021 cis-eQTLs for 14,329 genes and 4732 trans-eQTLs for 2612 genes. Genome-wide single gene expression association analysis was conducted by SMR software. The SMR analysis results were further subjected to gene set enrichment analysis (GSEA) to identify schizophrenia associated gene sets. SMR detected 49 genes significantly associated with schizophrenia. The top five significant genes were CRELD2 (p value = 1.65 × 10− 11), DIP2B (p value = 3.94 × 10− 11), ZDHHC18 (p value = 1.52 × 10− 10) and ZDHHC5 (p value = 7.45 × 10− 10), C11ORF75 (p value = 3.70 × 10− 9). GSEA identified 80 gene sets with p values < 0.01. The top five significant gene sets were COWLING_MYCN_TARGETS (p value < 0.001) and CHR16P11 (p value < 0.001), ACTACCT_MIR196A_MIR196B (p value = 0.002), CELLULAR_COMPONENT_DISASSEMBLY (p value = 0.002) and GRAESSMANN_RESPONSE_TO_MC_AND_DOXORUBICIN_DN (p value = 0.002). Our results provide useful information for revealing the genetic basis of schizophrenia.

源语言英语
页(从-至)50-54
页数5
期刊Progress in Neuro-Psychopharmacology and Biological Psychiatry
81
DOI
出版状态已出版 - 2 2月 2018
已对外发布

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