BDNF gene is a risk factor for schizophrenia in a Scottish population

被引:216
作者
Neves-Pereira, M
Cheung, J
Pasdar, A
Zhang, F
Breen, G
Yates, P
Sinclair, M
Crombie, C
Walker, N
St Clair, DM
机构
[1] Univ Aberdeen, Inst Med Sci, Dept Mental Hlth, Aberdeen AB25 2ZD, Scotland
[2] Univ London Kings Coll, Inst Psychiat, London WC2R 2LS, England
[3] Ravenscraig Hosp, Greenock, Scotland
[4] Aberdeen Royal Infirm, Aberdeen, Scotland
关键词
bipolar disorder; schizophrenia; association study; genetics; risk; haplotype analysis;
D O I
10.1038/sj.mp.4001575
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
Schizophrenia is a severe psychiatric disease with a strong genetic component. Brain-derived neurotrophic factor ( BDNF) has been implicated in the pathogenesis of schizophrenia and bipolar ( BP) disorders. The present study has examined two polymorphisms in linkage disequilibrium in the BDNF gene, which have been variously reported as associated with schizophrenia and BP. In our study, 321 probands with a primary diagnosis of schizophrenia or schizoaffective disorder, and 263 with a diagnosis of bipolar affective disorder, were examined together with 350 controls drawn from the same geographical region of Scotland. The val66met single-nucleotide polymorphism ( SNP) showed significant ( P = 0.005) association for valine ( allele G) with schizophrenia but not bipolar disorder. Haplotype analysis of val/ met SNP and a dinucleotide repeat polymorphism in the putative promoter region revealed highly significant ( P<1 x 10(-8)) under-representation of the methionine or met-1 haplotype in the schizophrenic but not the BP population. We conclude that, although the val66met polymorphism has been reported to alter gene function, the risk may depend upon the haplotypic background on which the val/ met variant is carried.
引用
收藏
页码:208 / 212
页数:5
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