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Association analysis of the glycogen synthase kinase-3β gene in bipolar disorder
被引:26
|作者:
Nishiguchi, N
Breen, G
Russ, C
St Clair, D
Collier, D
机构:
[1] Inst Psychiat, Dept Psychol Med, London SE5 8AF, England
[2] Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London SE5 8AF, England
[3] Kobe Univ, Grad Sch Med, Div Psychiat & Neurol, Dept Environm Hlth & Safety,Fac Med Sci,Chuo Ku, Kobe, Hyogo 6500017, Japan
[4] Univ Aberdeen, Dept Mental Hlth, Aberdeen AB25 2ZD, Scotland
基金:
英国医学研究理事会;
关键词:
manic depression;
affective disorder;
genetics;
wnt;
GSK3;
beta;
insulin;
presenilin;
Tau;
lithium;
allelic;
D O I:
10.1016/j.neulet.2005.10.042
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Glycogen synthase kinase-3 beta (GSK3 beta) is a target of lithium as well as sodium valproate, both of which are effective mood stabilizing prophylatics/treatments for bipolar disorder, a highly heritable psychiatric disorder. Though it is not clear whether the mood stabilizing effects of these drugs act directly through GSK3 beta, it is a good candidate for mediating at least part of lithium's action, and is an aetiological candidate gene for the disease itself. Recently, a potential locus for bipolar disorder was reported on chromosome 3q, close to 3q13.37 where GSK3 beta maps. We conducted an association study to test the hypothesis that polymorphism of GSK3 beta is involved in susceptibility to bipolar disorder by examining association between GSK3 beta-gene polymorphisms and bipolar disorder. Of the five polymorphisms we examined, three were very rare in the study population and were not examined further. Neither of the remaining two polymorphisms we examined showed association with bipolar disorder. Thus, it is unlikely that the GSK3 beta-gene is a risk factor for bipolar disorder in our sample, but we cannot exclude the gene completely as other unknown polymorphisms in the gene may increase susceptibility. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
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页码:243 / 245
页数:3
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