Edinburgh Research Explorer

Whole-genome association study of bipolar disorder

Research output: Contribution to journalArticle

  • P Sklar
  • J W Smoller
  • J Fan
  • M A R Ferreira
  • R H Perlis
  • K Chambert
  • V L Nimgaonkar
  • M B McQueen
  • S V Faraone
  • A Kirby
  • P I W de Bakker
  • M N Ogdie
  • M E Thase
  • G S Sachs
  • K Todd-Brown
  • S B Gabriel
  • C Sougnez
  • C Gates
  • B Blumenstiel
  • M Defelice
  • K G Ardlie
  • J Franklin
  • K A McGhee
  • A McLean
  • M VanBeck
  • A McQuillin
  • N J Bass
  • J Lawrence
  • A Anjorin
  • D Curtis
  • E M Scolnick
  • M J Daly
  • H M Gurling
  • S M Purcell

Related Edinburgh Organisations

Original languageEnglish
Pages (from-to)558-569
Number of pages12
JournalMolecular Psychiatry
Volume13
Issue number6
DOIs
Publication statusPublished - 1 Jun 2008

Abstract

We performed a genome-wide association scan in 1461 patients with bipolar (BP) 1 disorder, 2008 controls drawn from the Systematic Treatment Enhancement Program for Bipolar Disorder and the University College London sample collections with successful genotyping for 372,193 single nucleotide polymorphisms (SNPs). Our strongest single SNP results are found in myosin5B (MYO5B; P=1.66 x 10(-7)) and tetraspanin-8 (TSPAN8; P=6.11 x 10(-7)). Haplotype analysis further supported single SNP results highlighting MYO5B, TSPAN8 and the epidermal growth factor receptor (MYO5B; P=2.04 x 10(-8), TSPAN8; P=7.57 x 10(-7) and EGFR; P=8.36 x 10(-8)). For replication, we genotyped 304 SNPs in family-based NIMH samples (n=409 trios) and University of Edinburgh case-control samples (n=365 cases, 351 controls) that did not provide independent replication after correction for multiple testing. A comparison of our strongest associations with the genome-wide scan of 1868 patients with BP disorder and 2938 controls who completed the scan as part of the Wellcome Trust Case-Control Consortium indicates concordant signals for SNPs within the voltage-dependent calcium channel, L-type, alpha 1C subunit (CACNA1C) gene. Given the heritability of BP disorder, the lack of agreement between studies emphasizes that susceptibility alleles are likely to be modest in effect size and require even larger samples for detection.

    Research areas

  • Antigens, Neoplasm, Bipolar Disorder, Chromosome Mapping, DNA, Gene Frequency, Genetic Markers, Genome, Human, genotype, Humans, Medical History Taking, Membrane Glycoproteins, Myosin Heavy Chains, Myosin Type V, Patient Selection, Polymorphism, Single Nucleotide, Receptor, Epidermal Growth Factor, Reference Values, Tetraspanins

ID: 3188065