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The Translin-associated factor X/Disrupted in Schizophrenia 1 (TRAX/DISC) region was first implicated as a susceptibility locus for schizophrenia by analysis of a large Scottish family in which a t(1;11) translocation cosegregates with schizophrenia, bipolar disorder and recurrent major depression. We now report evidence for association between bipolar disorder and schizophrenia and this locus in the general Scottish population. A systematic study of linkage disequilibrium in a representative sample of the Scottish population was undertaken across the 510 kb of TRAX and DISC1. SNPs representing each haplotype block were selected for case-control association studies of both schizophrenia and bipolar disorder. Significant association with bipolar disorder in women P=0.00026 (P=0.0016 in men and women combined) was detected in a region of DISC1. This same region also showed nominally significant association with schizophrenia in both men and women combined, P=0.0056. Two further regions, one in TRAX and the second in DISC1, showed weaker evidence for sex-specific associations of individual haplotypes with bipolar disorder in men and women respectively, P<0.01. Only the association between bipolar women and DISC1 remained significant after correction for multiple testing. This result provides further supporting evidence for DISC1 as a susceptibility factor for both bipolar disorder and schizophrenia, consistent with the diagnoses in the original Scottish translocation family.

Original publication

DOI

10.1038/sj.mp.4001669

Type

Journal article

Journal

Molecular psychiatry

Publication Date

07/2005

Volume

10

Pages

657 - 616

Addresses

Medical Genetics Section, University of Edinburgh, Molecular Medicine Centre, Western General Hospital, Edinburgh, UK. Pippa.Thomson@ed.ac.uk

Keywords

Humans, Genetic Predisposition to Disease, DNA-Binding Proteins, Nerve Tissue Proteins, Statistics, Nonparametric, Case-Control Studies, Pedigree, Bipolar Disorder, Schizophrenia, Sex Factors, Haplotypes, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Scotland, Female, Male