Brain-derived neurotrophic factor (BDNF) gene and rapid-cycling bipolar disorder -: Family-based association study

被引:83
作者
Mueller, Daniel J.
De Luca, Vincenzo
Sicard, Tricia
King, Nicole
Strauss, John
Kennedy, James L.
机构
[1] Univ Toronto, Dept Psychiat, Ctr Addict & Mental Hlth, Neurogenet Sect, Toronto, ON M5T 1R8, Canada
[2] Univ Berlin, Charite, Berlin, Germany
关键词
D O I
10.1192/bjp.bp.105.010587
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background We have previously reported the Val66Met and GT(n) repeat polymorphisms of the brain-derived neurotrophic factor (BDNF) gene to be associated with bipolar disorder. However, these findings have not been replicated consistently. Aims To dissect the association of the BDNF gene with bipolar disorder by examining additional markers at the DNA level and by testing the illness categories of bipolar disorder I and II and rapid cycling. Method We performed a family-based association study and haplotype analyses with 312 nuclear families using four single nucleotide polymorphisms (SNPs) and the Val66Met and GT(n) repeat polymorphisms. Results The SNPs hCVII592756 and rs2049045, the Val66 Met and GT(n) were significantly associated with bipolar disorder using transmission disequilibrium analyses (P=0.02, 0.009, 0.001 and 0.008 respectively). The effect at these markers was mainly driven by the rapid-cycling patients. Conclusions Within bipolar disorder, variation in the BDNF gene appears to predict risk for developing rapid cycling according to DSM-IV. Incorporating this clinical sub-phenotyping into other studies of the BDNF gene may help to resolve some of the inconsistencies reported thus far concerning BDNF and bipolar disorder. Declaration of Interest None. Funding detailed in Acknowledgements.
引用
收藏
页码:317 / 323
页数:7
相关论文
共 32 条
[1]   Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[2]   Early age at onset as a risk factor for poor outcome of bipolar disorder [J].
Carter, TDC ;
Mundo, E ;
Parikh, SV ;
Kennedy, JL .
JOURNAL OF PSYCHIATRIC RESEARCH, 2003, 37 (04) :297-303
[3]  
Cichon S, 2004, AM J MED GENET B, V130B, P27
[4]   Pedigree disequilibrium tests for multilocus haplotypes [J].
Dudbridge, F .
GENETIC EPIDEMIOLOGY, 2003, 25 (02) :115-121
[5]  
DUNNER DL, 1974, ARCH GEN PSYCHIAT, V30, P229
[6]   The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function [J].
Egan, MF ;
Kojima, M ;
Callicott, JH ;
Goldberg, TE ;
Kolachana, BS ;
Bertolino, A ;
Zaitsev, E ;
Gold, B ;
Goldman, D ;
Dean, M ;
Lu, B ;
Weinberger, DR .
CELL, 2003, 112 (02) :257-269
[7]   Linkage disequilibrium of the brain-derived neurotrophic factor Val66Met polymorphism in children with a prepubertal and early adolescent bipolar disorder phenotype [J].
Geller, B ;
Badner, JA ;
Tillman, R ;
Christian, SL ;
Bolhofner, K ;
Cook, EH .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (09) :1698-1700
[8]   Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder - Case-control study of over 3000 individuals from the UK [J].
Green, EK ;
Raybould, R ;
MacGregor, S ;
Hyde, S ;
Young, AH ;
O'Donovan, MC ;
Owen, MJ ;
Kirov, G ;
Jones, L ;
Jones, I ;
Craddock, N .
BRITISH JOURNAL OF PSYCHIATRY, 2006, 188 :21-25
[9]   Sequence variants of the brain-derived neurotrophic factor (BDNF) gene are strongly associated with obsessive-compulsive disorder [J].
Hall, D ;
Dhilla, A ;
Charalambous, A ;
Gogos, JA ;
Karayiorgou, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (02) :370-376
[10]   Association study of a brain-derived neurotrophic-factor genetic polymorphism and mood disorders, age of onset and suicidal behavior [J].
Hong, CJ ;
Huo, SJ ;
Yen, FC ;
Tung, CL ;
Pan, GM ;
Tsai, SJ .
NEUROPSYCHOBIOLOGY, 2003, 48 (04) :186-189