Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder - Case-control study of over 3000 individuals from the UK

被引:105
作者
Green, EK
Raybould, R
MacGregor, S
Hyde, S
Young, AH
O'Donovan, MC
Owen, MJ
Kirov, G
Jones, L
Jones, I
Craddock, N
机构
[1] Cardiff Univ, Wales Coll Med, Dept Med Psychol, Cardiff CF4 4XN, Wales
[2] Cardiff Univ, Wales Coll Med, Biostat & Bioinformat Unit, Cardiff CF4 4XN, Wales
[3] Univ Birmingham, Queen Elizabeth Psychiat Hosp, Div Neurosci, Birmingham B15 2TH, W Midlands, England
[4] Newcastle Univ, Dept Psychiat, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国医学研究理事会;
关键词
D O I
10.1192/bjp.bp.105.009969
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Brain-derived neurotrophic factor (BDNF) influences neuronal survival, proliferation and plasticity. Three family-based studies have shown association of the common Valine (Val) allele of the Val 66Met polymorphism of the BDNF gene with susceptibility to bipolar disorder. Aims To replicate this finding. Method We genotyped the Val66Met polymorphism in our UK White bipolar case-control sample (n=3062). Results We found no overall evidence of allele or genotype association. However, we found association with disease status in the subset of 131 individuals that had experienced rapid cycling at some time (P=0.004). We found a similar association on re-analysis of our previously reported family-based association sample (P < 0.03, one-tailed test). Conclusions Variation at the Val 66 Met polymorphism of BDNF does not play a major role in influencing susceptibility to bipolar disorder as a whole, but is associated with susceptibility to the rapid-cycling subset of the disorder. Declaration of interest N.C. and M.J.O. are consultants to GlaxoSmith Kline and have received grant funding and honoraria from GlaxoSmith Kline, AstraZeneca and Eli Lilly. M.C. O'D., A.H.Y., L.J. and G.K. have received honoraria from GlaxoSmith Kline, AstraZeneca and Eli Lilly G.K. has received grant funding from Janssen. Funding detailed in Acknowledgements.
引用
收藏
页码:21 / 25
页数:5
相关论文
共 32 条
[21]  
MULLER DJ, 2006, IN PRESS BRIT J PSYC
[22]   Association study of the brain-derived neurotrophic factor (BDNF) gene with bipolar disorder [J].
Nakata, K ;
Ujike, H ;
Sakai, A ;
Uchida, N ;
Nomura, A ;
Imamura, T ;
Katsu, T ;
Tanaka, Y ;
Hamamura, T ;
Kuroda, S .
NEUROSCIENCE LETTERS, 2003, 337 (01) :17-20
[23]   BDNF gene is a risk factor for schizophrenia in a Scottish population [J].
Neves-Pereira, M ;
Cheung, J ;
Pasdar, A ;
Zhang, F ;
Breen, G ;
Yates, P ;
Sinclair, M ;
Crombie, C ;
Walker, N ;
St Clair, DM .
MOLECULAR PSYCHIATRY, 2005, 10 (02) :208-212
[24]   The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: Evidence from a family-based association study [J].
Neves-Pereira, M ;
Mundo, E ;
Muglia, P ;
King, N ;
Macciardi, F ;
Kennedy, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (03) :651-655
[25]   DIAGNOSTIC INTERVIEW FOR GENETIC-STUDIES - RATIONALE, UNIQUE FEATURES, AND TRAINING [J].
NURNBERGER, JI ;
BLEHAR, MC ;
KAUFMANN, CA ;
YORKCOOLER, C ;
SIMPSON, SG ;
HARKAVYFRIEDMAN, J ;
SEVERE, JB ;
MALASPINA, D ;
REICH, T ;
MILLER, M ;
BOWMAN, ES ;
DEPAULO, JR ;
CLONINGER, CR ;
ROBINSON, G ;
MODLIN, S ;
GERSHON, ES ;
MAXWELL, E ;
GUROFF, JJ ;
KIRCH, D ;
WYNNE, D ;
BERG, K ;
TSUANG, MT ;
FARAONE, SV ;
PEPPLE, JR ;
RITZ, AL .
ARCHIVES OF GENERAL PSYCHIATRY, 1994, 51 (11) :849-859
[26]   Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: A Belgian patient-control study [J].
Oswald, P ;
Del-Favero, J ;
Massat, I ;
Souery, D ;
Claes, S ;
Van Broeckhoven, C ;
Mendlewicz, J .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 129B (01) :34-35
[27]  
PURCELL S, 2003, BIOINFORMATICS, V19, P149, DOI [DOI 10.1093/BIOINFORMATICS/19.1.149, 10.1093/bioinformatics/19.1.149]
[28]   Association analysis of brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism in schizophrenia and bipolar affective disorder [J].
Skibinska, M ;
Hauser, J ;
Czerski, PM ;
Leszczynska-Rodziewicz, A ;
Losmowska, M ;
Kapelski, P ;
Slopien, A ;
Zakrzewska, M ;
Rybakowski, JK .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2004, 5 (04) :215-220
[29]   Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus [J].
Sklar, P ;
Gabriel, SB ;
McInnis, MG ;
Bennett, P ;
Lim, YM ;
Tsan, G ;
Schaffner, S ;
Kirov, G ;
Jones, I ;
Owen, M ;
Craddock, N ;
DePaulo, JR ;
Lander, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (06) :579-593
[30]  
SPIELMAN RS, 1993, AM J HUM GENET, V52, P506