Literature DB >> 16984960

Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34.

Ibi Herzberg1, Anna Jasinska, Jenny García, Damini Jawaheer, Susan Service, Barbara Kremeyer, Constanza Duque, María V Parra, Jorge Vega, Daniel Ortiz, Luis Carvajal, Guadalupe Polanco, Gabriel J Restrepo, Carlos López, Carlos Palacio, Matthew Levinson, Ileana Aldana, Carol Mathews, Pablo Davanzo, Julio Molina, Eduardo Fournier, Julio Bejarano, Magui Ramírez, Carmen Araya Ortiz, Xinia Araya, Chiara Sabatti, Victor Reus, Gabriel Macaya, Gabriel Bedoya, Jorge Ospina, Nelson Freimer, Andrés Ruiz-Linares.   

Abstract

We performed a whole genome microsatellite marker scan in six multiplex families with bipolar (BP) mood disorder ascertained in Antioquia, a historically isolated population from North West Colombia. These families were characterized clinically using the approach employed in independent ongoing studies of BP in the closely related population of the Central Valley of Costa Rica. The most consistent linkage results from parametric and non-parametric analyses of the Colombian scan involved markers on 5q31-33, a region implicated by the previous studies of BP in Costa Rica. Because of these concordant results, a follow-up study with additional markers was undertaken in an expanded set of Colombian and Costa Rican families; this provided a genome-wide significant evidence of linkage of BPI to a candidate region of approximately 10 cM in 5q31-33 (maximum non-parametric linkage score=4.395, P<0.00004). Interestingly, this region has been implicated in several previous genetic studies of schizophrenia and psychosis, including disease association with variants of the enthoprotin and gamma-aminobutyric acid receptor genes.

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Year:  2006        PMID: 16984960     DOI: 10.1093/hmg/ddl254

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


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