4.4 Article

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

Journal

SCHIZOPHRENIA RESEARCH
Volume 138, Issue 1, Pages 69-73

Publisher

ELSEVIER
DOI: 10.1016/j.schres.2012.03.007

Keywords

Association; Genetic overlap; Manic depression; Psychotic disorder; Cortex; Hippocampus

Categories

Funding

  1. German Federal Ministry of Education and Research (BMBF)
  2. Integrated Genome Research Network (IG) MooDS [01GS08144, 01GS08147]
  3. IZKF, Medical School, Jena University Hospital
  4. EU (EUTwinsS network, RTN)
  5. German Research Foundation [GRK 793]
  6. Medical Faculty of the University Hospital of Essen
  7. Helmholtz Zentrum Munchen - National Research Center for Environmental Health
  8. BMBF
  9. State of Bavaria
  10. NGFN [01GS0823]
  11. Munich Center of Health Sciences (MC Health) as part of LMUinnovativ
  12. NIMH [R01 MH078075, R01 MH67257, R01 MH59588, R01 MH59571, R01 MH59565, R01 MH59587, R01 MH60870, R01 MH59566, R01 MH59586, R01 MH61675, R01 MH60879, R01 MH81800, U01 MH46276, U01 MH46289, U01 MH46318, U01 MH79469, U01 MH79470]
  13. Genetic Association Information Network (GAIN)
  14. [U01 HL089856]
  15. [R01 MH087590]
  16. [R01 MH081862]

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A recent study found genome-wide significant association between common variation in the gene neurocan (NCAN, rs1064395) and bipolar disorder (BD). In view of accumulating evidence that BD and schizophrenia partly share genetic risk factors, we tested this single-nucleotide polymorphism for association with schizophrenia in three independent patient-control samples of European ancestry, totaling 5061 patients and 9655 controls. The rs1064395 A-allele, which confers risk for BD, was significantly over-represented in schizophrenia patients compared to controls (p=2.28x10(-3); odds ratio=1.11). Follow-up in non-overlapping samples from the Schizophrenia Psychiatric GWAS Consortium (5537 patients, 8043 controls) provided further support for our finding (p=0.0239, odds ratio=1.07). Our data suggest that genetic variation in NCAN is a common risk factor for BD and schizophrenia. (C) 2012 Elsevier B.V. All rights reserved.

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