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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near odz4

Academic Article
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Overview

authors

  • Sklar, P.
  • Ripke, S.
  • Scott, L. J.
  • Andreassen, O. A.
  • Cichon, S.
  • Craddock, N.
  • Edenberg, H. J.
  • Nurnberger, J. I.
  • Rietschel, M.
  • Blackwood, D.
  • Corvin, A.
  • Flickinger, M.
  • Guan, W. H.
  • Mattingsdal, M.
  • McQuillin, A.
  • Kwan, P.
  • Wienker, T. F.
  • Daly, M.
  • Dudbridge, F.
  • Holmans, P. A.
  • Lin, D. Y.
  • Burmeister, M.
  • Greenwood, T. A.
  • Hamshere, M. L.
  • Muglia, P.
  • Smith, E. N.
  • Zandi, P. P.
  • Nievergelt, C. M.
  • McKinney, R.
  • Shilling, P. D.
  • Schork, Nicholas
  • Bloss, C. S.
  • Foroud, T.
  • Koller, D. L.
  • Gershon, E. S.
  • Liu, C. Y.
  • Badner, J. A.
  • Scheftner, W. A.
  • Lawson, W. B.
  • Nwulia, E. A.
  • Hipolito, M.
  • Coryell, W.
  • Rice, John
  • Byerley, W.
  • McMahon, F. J.
  • Schulze, T. G.
  • Berrettini, W.
  • Lohoff, F. W.
  • Potash, J. B.
  • Mahon, P. B.
  • McInnis, M. G.
  • Zollner, S.
  • Zhang, P.
  • Craig, D. W.
  • Szelinger, S.
  • Barrett, T. B.
  • Breuer, R.
  • Meier, S.
  • Strohmaier, J.
  • Witt, S. H.
  • Tozzi, F.
  • Farmer, A.
  • McGuffin, P.
  • Strauss, J.
  • Xu, W.
  • Kennedy, J. L.
  • Vincent, J. B.
  • Matthews, K.
  • Day, R.
  • Ferreira, M. A.
  • O'Dushlaine, C.
  • Perlis, R.
  • Raychaudhuri, S.
  • Ruderfer, D.
  • Hyoun, P. L.
  • Smoller, J. W.
  • Li, J.
  • Absher, D.
  • Thompson, R. C.
  • Meng, F. G.
  • Schatzberg, A. F.
  • Bunney, W. E.
  • Barchas, J. D.
  • Jones, E. G.
  • Watson, S. J.
  • Myers, R. M.
  • Akil, H.
  • Boehnke, M.
  • Chambert, K.
  • Moran, J.
  • Scolnick, E.
  • Djurovic, S.
  • Melle, I.
  • Morken, G.
  • Gill, Matt
  • Morris, D.
  • Quinn, E.
  • Muhleisen, T. W.
  • Degenhardt, F. A.
  • Mattheisen, M.
  • Schumacher, J.
  • Maier, W.
  • Steffens, M.
  • Propping, P.
  • Nothen, M. M.
  • Anjorin, A.
  • Bass, N.
  • Gurling, H.
  • Kandaswamy, R.
  • Lawrence, J.
  • McGhee, K.
  • McIntosh, A.
  • McLean, A. W.
  • Muir, W. J.
  • Pickard, B. S.
  • Breen, G.
  • St Clair, D.
  • Caesar, S.
  • Gordon-Smith, K.
  • Jones, L.
  • Fraser, C.
  • Green, E. K.
  • Grozeva, D.
  • Jones, I. R.
  • Kirov, G.
  • Moskvina, V.
  • Nikolov, I.
  • O'Donovan, M. C.
  • Owen, M. J.
  • Collier, D. A.
  • Elkin, A.
  • Williamson, R.
  • Young, A. H.
  • Ferrier, I. N.
  • Stefansson, K.
  • Stefansson, H.
  • Porgeirsson, P.
  • Steinberg, S.
  • Gustafsson, O.
  • Bergen, S. E.
  • Nimgaonkar, V.
  • Hultman, C.
  • Landen, M.
  • Lichtenstein, P.
  • Sullivan, P.
  • Schalling, M.
  • Osby, U.
  • Backlund, L.
  • Frisen, L.
  • Langstrom, N.
  • Jamain, S.
  • Leboyer, M.
  • Etain, B.
  • Bellivier, F.
  • Petursson, H.
  • Sigurosson, E.
  • Muller-Mysok, B.
  • Lucae, S.
  • Schwarz, M.
  • Schofield, P. R.
  • Martin, N.
  • Montgomery, G. W.
  • Lathrop, M.
  • Oskarsson, H.
  • Bauer, M.
  • Wright, A.
  • Mitchell, P. B.
  • Hautzinger, M.
  • Reif, A.
  • Kelsoe, J. R.
  • Purcell, S. M.
  • Psychiat, Gwas Consortium Bipolar D.

publication date

  • October 2011

journal

  • Nature Genetics  Journal

abstract

  • We conducted a combined genome-wide association study (GWAS) of 7,481 individuals with bipolar disorder (cases) and 9,250 controls as part of the Psychiatric GWAS Consortium. Our replication study tested 34 SNPs in 4,496 independent cases with bipolar disorder and 42,422 independent controls and found that 18 of 34 SNPs had P < 0.05, with 31 of 34 SNPs having signals with the same direction of effect (P = 3.8 × 10(-7)). An analysis of all 11,974 bipolar disorder cases and 51,792 controls confirmed genome-wide significant evidence of association for CACNA1C and identified a new intronic variant in ODZ4. We identified a pathway comprised of subunits of calcium channels enriched in bipolar disorder association intervals. Finally, a combined GWAS analysis of schizophrenia and bipolar disorder yielded strong association evidence for SNPs in CACNA1C and in the region of NEK4-ITIH1-ITIH3-ITIH4. Our replication results imply that increasing sample sizes in bipolar disorder will confirm many additional loci.

subject areas

  • Alleles
  • Bipolar Disorder
  • Calcium Channels, L-Type
  • Case-Control Studies
  • Databases, Genetic
  • Genetic Loci
  • Genetic Predisposition to Disease
  • Genome, Human
  • Genome-Wide Association Study
  • Humans
  • Linkage Disequilibrium
  • Nuclear Proteins
  • Polymorphism, Single Nucleotide
  • Schizophrenia
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Identity

PubMed Central ID

  • PMC3637176

International Standard Serial Number (ISSN)

  • 1061-4036

Digital Object Identifier (DOI)

  • 10.1038/ng.943

PubMed ID

  • 21926972
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Additional Document Info

start page

  • 977

end page

  • 983

volume

  • 43

issue

  • 10

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