Psychiatric Genetics

Skip Navigation LinksHome > June 2010 - Volume 20 - Issue 3 > Support for a bipolar affective disorder susceptibility locu...
Psychiatric Genetics:
doi: 10.1097/YPG.0b013e32833a2066
Original Articles

Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3

Buttenchøn, Henriette Nørmøllea; Foldager, Lesliea b; Flint, Tracey J.a; Olsen, Inger Marie L.a; Deleuran, Thomasa; Nyegaard, Mettec; Hansen, Mette M.a; Kallunki, Pekkad; Christensen, Kenneth V.d; Blackwood, Douglas H.f; Muir, Walter J.f; Straarup, Steen E.a; Als, Thomas D.a; Nordentoft, Meretee; Børglum, Anders D.a c; Mors, Olea

Supplemental Author Material


In the article that appeared on page 93 of the June 2010 issue, an author's name was misspelled. The author's name should have appeared as Henriette Nørmølle Buttenschøn (Buttenschøn et al., 2010).

Psychiatric Genetics. 20(5):272, October 2010.

Collapse Box


Objective Linkage and association studies of bipolar affective disorder (BAD) point out chromosome 12q24 as a region of interest.

Methods To investigate this region further, we conducted an association study of 22 DNA markers within a 1.14 Mb region in a Danish sample of 166 patients with BAD and 311 control individuals. Two-hundred and four Danish patients with schizophrenia were also included in the study.

Results We observed highly significant allelic and genotypic association between BAD and two highly correlated markers. The risk allele of both markers considered separately conferred an odds ratio of 2 to an individual carrying one risk allele and an odds ratio of 4 for individuals carrying both risk alleles assuming an additive genetic model. These findings were supported by the haplotype analysis. In addition, we obtained a replication of four markers associated with BAD in an earlier UK study.

The most significantly associated marker was also analyzed in a Scottish case–control sample and was earlier associated with BAD in the UK cohort. The association of that particular marker was strongly associated with BAD in a meta-analysis of the Danish, Scottish and UK sample (P=0.0003).

The chromosome region confined by our most distant markers is gene-poor and harbours only a few predicted genes. This study implicates the Slynar locus. We confirmed one annotated Slynar transcript and identified a novel transcript in human brain cDNA.

Conclusion This study confirms 12q24.3 as a region of functional importance in the pathogenesis of BAD and highlights the importance of focused genotyping.

© 2010 Lippincott Williams & Wilkins, Inc.


Article Tools


Article Level Metrics

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.