期刊
BIOLOGICAL PSYCHIATRY
卷 70, 期 1, 页码 35-42出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2011.01.030
关键词
Complement cascade; csmd1; csmd2; human leukocyte antigen (HLA); immunity; schizophrenia
资金
- Research Council of Norway [186001, 151904, 183327, 167153/V50, 163070/V50]
- Helse Vest RHF
- Dr. Einar Martens Fund
- German Federal Ministry of Education and Research (BMBF)
- Integrated Genome Research Network (IG) [01GS08144, 01GS08147]
- Alfried Krupp von Bohlen und Halbach-Stiftung
- Munich Center of Health Sciences (MC Health)
- Heinz Nixdorf Foundation
- South-East Norway Health Authority [2004-123]
- University of Oslo
Background: Patients with schizophrenia often suffer from cognitive dysfunction, including impaired learning and memory. We recently demonstrated that long-term potentiation in rat hippocampus, a mechanistic model of learning and memory, is linked to gene expression changes in immunity-related processes involved in complement activity and antigen presentation. We therefore aimed to examine whether key regulators of these processes are genetic susceptibility factors in schizophrenia. Methods: Analysis of genetic association was based on data mining of genotypes from a German genome-wide association study and a multiplex GoldenGate tag single nucleotide polymorphism (SNP)-based assay of Norwegian and Danish case-control samples (Scandinavian Collaboration on Psychiatric Etiology), including 1133 patients with schizophrenia and 2444 healthy control subjects. Results: Allelic associations were found across all three samples for eight common SNPs in the complement control-related gene CSMD2 (CUB and Sushi Multiple Domains 2) on chromosome 1p35.1-34.3, of which rs911213 reached a statistical significance comparable to that of a genome wide threshold (p value = 4.0 x 10(-8); odd ratio = .73, 95% confidence interval = .65-.82). The second most significant gene was CSMD1 on chromosome 8p23.2, a homologue to CSMD2. In addition, we observed replicated associations in the complement surface receptor CD46 as well as the major histocompatibility complex genes HLA-DMB and HLA-DOA. Conclusions: These data demonstrate a significant role of complement control-related genes in the etiology of schizophrenia and support disease mechanisms that involve the activity of immunity-related pathways in the brain.
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