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PMID: 8917544 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

McInnes LA, Escamilla MA, Service SK, Reus VI, Leon P, Silva S, Rojas E, Spesny M, Baharloo S, Blankenship K, Peterson A, Tyler D, Shimayoshi N, Tobey C, Batki S, Vinogradov S, Meza L, Gallegos A, Fournier E, Smith LB, Barondes SH, Sandkuijl LA, Freimer NB

Abstract

Bipolar mood disorder (BP) is a debilitating syndrome characterized by episodes of mania and depression. We designed a multistage study to detect all major loci predisposing to severe BP (termed BP-I) in two pedigrees drawn from the Central Valley of Costa Rica, where the population is largely descended from a few founders in the 16th-18th centuries. We considered only individuals with BP-I as affected and screened the genome for linkage with 473 microsatellite markers. We used a model for linkage analysis that incorporated a high phenocopy rate and a conservative estimate of penetrance. Our goal in this study was not to establish definitive linkage but rather to detect all regions possibly harboring major genes for BP-I in these pedigrees. To facilitate this aim, we evaluated the degree to which markers that were informative in our data set provided coverage of each genome region; we estimate that at least 94% of the genome has been covered, at a predesignated threshold determined through prior linkage simulation analyses. We report here the results of our genome screen for BP-I loci and indicate several regions that merit further study, including segments in 18q, 18p, and 11p, in which suggestive lod scores were observed for two or more contiguous markers. Isolated lod scores that exceeded our thresholds in one or both families also occurred on chromosomes 1, 2, 3, 4, 5, 7, 13, 15, 16, and 17. Interesting regions highlighted in this genome screen will be followed up using linkage disequilibrium (LD) methods.

MeSH Terms
Bipolar Disorder/genetics Chromosome Mapping Chromosomes, Human, Pair 18 Costa Rica Female Genes, Dominant Genetic Linkage Genetic Markers Genome, Human Humans Lod Score Male Microsatellite Repeats Models, Genetic Pedigree
Chemicals
Genetic Markers
Authors & Affiliations
23 authors, click to expand affiliations / ORCID
McInnes L A
Neurogenetics Laboratory, University of California, San Francisco 94143, USA.
Escamilla M A
Service S K
Reus V I
Leon P
Silva S
Rojas E
Spesny M
Baharloo S
Blankenship K
Peterson A
Tyler D
Shimayoshi N
Tobey C
Batki S
Vinogradov S
Meza L
Gallegos A
Fournier E
Smith L B
Barondes S H
Sandkuijl L A
Freimer N B
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1996-11-12
Pages
13060-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC24046
Subset
IM
Grants
NIMH NIH HHS · R01 MH049499 · United States
NIMH NIH HHS · MH00916 · United States
NIMH NIH HHS · MH48695 · United States
NIMH NIH HHS · MH49499 · United States
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