4.4 Article

Genetic liability for schizophrenia predicts risk of immune disorders

期刊

SCHIZOPHRENIA RESEARCH
卷 159, 期 2-3, 页码 347-352

出版社

ELSEVIER
DOI: 10.1016/j.schres.2014.09.004

关键词

Polygenic risk score; Genetic overlap; Genome-wide association study; Immune dysregulation; Human leukocyte antigen system; Major histocompatibility complex

资金

  1. Netherlands Scientific Organization (NWO) [451-08-010]
  2. National Institute of Mental Health at the National Institutes of Health [NIH/NIMH R01 MH078075]
  3. MRC [G1001799] Funding Source: UKRI
  4. Medical Research Council [G1001799] Funding Source: researchfish

向作者/读者索取更多资源

Background: Schizophrenia patients and their parents have an increased risk of immune disorders compared to population controls and their parents. This may be explained by genetic overlap in the pathogenesis of both types of disorders. The purpose of this study was to investigate the genetic overlap between schizophrenia and three immune disorders and to compare with the overlap between schizophrenia and two disorders not primarily characterized by immune dysregulation: bipolar disorder and type 2 diabetes. Methods: We performed a polygenic risk score analysis using results from the schizophrenia Psychiatric GWAS consortium (PGC) (8922 cases and 9528 controls) and five Wellcome Trust Case Control Consortium (WTCCC) case samples as target cases: bipolar disorder (n = 1998), type 1 diabetes (n = 2000), Crohn's diseases (n = 2005), rheumatoid arthritis (n = 1999), and type 2 diabetes (n = 1999). The WTCCC British Birth Cohort and National Blood Service samples (n = 3004) were used as target controls. Additionally, we tested whether schizophrenia polygenic risk scores significantly differed between patients with immune disorder, bipolar disorder, and type 2 diabetes respectively. Results: Polygenic risk scores for schizophrenia significantly predicted disease status in all three immune disorder samples (Nagelkerke-R-2 1.1%-1.3%; p < 0.05). The polygenic risk of schizophrenia in patients with immune disorders was significantly lower than in patients with bipolar disorder (Nagelkerke-R-2 6.0%; p < 0.05), but higher than in type 2 diabetes patients (Nagelkerke-R-2 0.5%; p < 0.05). Conclusions: Our results suggest that genetic factors are shared between schizophrenia and immune disorders. This contributes to an accumulating body of evidence that immune processes may play a role in the etiology of schizophrenia. (C) 2014 Elsevier B. V. All rights reserved.

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