Bipolar disorder or manic-depressive illness is a major psychiatric illness that affects 1% of the world's population. It is characterized by alternation between the two extreme mood states of mania and depression. Psychosis can occur in either state and the lifetime suicide rate is 17%. Our 11 site consortium has been funded for over 15 years to collect DMA samples from patients with bipolar disorder and their families for genetic studies. We were recently selected by GAIN to be one of six diseases to be genotyped for whole genome association studies. GAIN will sponsor genotyping of 1158 Caucasian and 400 African American bipolar I cases. Controls will be shared with a corresponding project on schizophrenia (principal investigator: P. Gejman). These samples will be genotyped by the Broad Institute under contract from GAIN using the Affymetrix 500Kb chip. This will provide genotypes on approximately 500,000 SNPs and data on copy number variation genome-wide. The analyses will be conducted on a collaborative basis by 6 collaborating sites each of whom participated in the sample collection. UCSD will serve as the lead site and will be responsible for coordinating the analytic work between the participating sites. The case-control samples will be examined for population substructure and this information will be used as a covariate in the association analysis. Both single SNP and haplotype based methods will be employed for analysis of association. Gene-gene interactions will also be examined. Several possible genetically distinct subforms of illness will also be examined separately. Relevant genes and regions from the genome-wide association will be selected for replication in a second independent sample of 1,000 Caucasian cases and 1,000 controls, and 200 African-American cases and 200 controls. Replicated genes will be subjected to pathway analysis in an attempt to identify pathways involved in mechanisms of disease. Support is requested for the UCSD site in order to coordinate analytic effort between the sites, provide database, bioinformatic and statistical support for all the sites and to conduct the primary analysis of the data. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH081804-01
Application #
7343400
Study Section
Special Emphasis Panel (ZMH1-ERB-C (02))
Program Officer
Lehner, Thomas
Project Start
2007-09-27
Project End
2009-09-26
Budget Start
2007-09-27
Budget End
2009-09-26
Support Year
1
Fiscal Year
2007
Total Cost
$154,500
Indirect Cost
Name
University of California San Diego
Department
Psychiatry
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Liu, Xiaohua; Bipolar Genome Study (BiGS); Kelsoe, John R et al. (2016) A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region. J Affect Disord 189:141-9
Swaminathan, Shanker; Koller, Daniel L; Foroud, Tatiana et al. (2015) Characteristics of Bipolar I patients grouped by externalizing disorders. J Affect Disord 178:206-14
Jacobsen, Kaya K; Nievergelt, Caroline M; Zayats, Tetyana et al. (2015) Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. J Affect Disord 172:453-61
Nurnberger Jr, John I; Koller, Daniel L; Jung, Jeesun et al. (2014) Identification of pathways for bipolar disorder: a meta-analysis. JAMA Psychiatry 71:657-64
Lee, Heon-Jeong; Woo, Hyun Goo; Greenwood, Tiffany A et al. (2013) A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder. J Affect Disord 145:200-7
Greenwood, Tiffany A; Bipolar Genome Study (BiGS) Consortium; Kelsoe, John R (2013) Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. PLoS One 8:e53804
Nissen, Stephanie; Liang, Sherri; Shehktman, Tatyana et al. (2012) Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. Am J Med Genet B Neuropsychiatr Genet 159B:941-50
Greenwood, Tiffany A; Akiskal, Hagop S; Akiskal, Kareen K et al. (2012) Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci. Biol Psychiatry 72:303-10
Zhang, Dandan; Qian, Yudong; Akula, Nirmala et al. (2011) Accuracy of CNV Detection from GWAS Data. PLoS One 6:e14511
Psychiatric GWAS Consortium Bipolar Disorder Working Group (2011) Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet 43:977-83

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