Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

被引:133
作者
Thomson, PA
Wray, NR
Millar, JK
Evans, KL
Le Hellard, S
Condie, A
Muir, WJ
Blackwood, DHR
Porteous, DJ
机构
[1] Univ Edinburgh, Western Gen Hosp, Mol Med Ctr, Dept Med Sci,Med Genet Sect, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Royal Edinburgh Hosp, Dept Psychiat, Edinburgh EH10 5HF, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
bipolar disorder; schizophrenia; DISC1; TRAX; association; neurodevelopment;
D O I
10.1038/sj.mp.4001669
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:657 / 668
页数:12
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