Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia

被引:58
作者
Mathieson, I.
Munafo, M. R. [2 ]
Flint, J. [1 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[2] Univ Bristol, Sch Expt Psychol, Bristol, Avon, England
基金
英国惠康基金;
关键词
association; case-control; DISC1; GWAS; meta-analysis; schizophrenia; GENOME-WIDE ASSOCIATION; GENETIC ASSOCIATION; SCOTTISH POPULATION; NEURITE OUTGROWTH; BIPOLAR DISORDER; CANDIDATE GENES; RISK; DISRUPTED-IN-SCHIZOPHRENIA-1; IDENTIFICATION; POLYMORPHISMS;
D O I
10.1038/mp.2011.41
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
Several polymorphisms in the Disrupted-in-Schizophrenia-1 (DISC1) gene are reported to be associated with schizophrenia. However, to date, there has been little effort to evaluate the evidence for association systematically. We carried out an imputation-driven meta-analysis, the most comprehensive to date, using data collected from 10 candidate gene studies and three genome-wide association studies containing a total of 11 626 cases and 15 237 controls. We tested 1241 single-nucleotide polymorphisms in total, and estimated that our power to detect an effect from a variant with minor allele frequency > 5% was 99% for an odds ratio of 1.5 and 51% for an odds ratio of 1.1. We find no evidence that common variants at the DISC1 locus are associated with schizophrenia. Molecular Psychiatry (2012) 17, 634-641; doi:10.1038/mp.2011.41; published online 12 April 2011
引用
收藏
页码:634 / 641
页数:8
相关论文
共 61 条
  • [1] Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database
    Allen, Nicole C.
    Bagade, Sachin
    McQueen, Matthew B.
    Ioannidis, John P. A.
    Kavvoura, Fotini K.
    Khoury, Muin J.
    Tanzi, Rudolph E.
    Bertram, Lars
    [J]. NATURE GENETICS, 2008, 40 (07) : 827 - 834
  • [2] A map of human genome variation from population-scale sequencing
    Altshuler, David
    Durbin, Richard M.
    Abecasis, Goncalo R.
    Bentley, David R.
    Chakravarti, Aravinda
    Clark, Andrew G.
    Collins, Francis S.
    De la Vega, Francisco M.
    Donnelly, Peter
    Egholm, Michael
    Flicek, Paul
    Gabriel, Stacey B.
    Gibbs, Richard A.
    Knoppers, Bartha M.
    Lander, Eric S.
    Lehrach, Hans
    Mardis, Elaine R.
    McVean, Gil A.
    Nickerson, DebbieA.
    Peltonen, Leena
    Schafer, Alan J.
    Sherry, Stephen T.
    Wang, Jun
    Wilson, Richard K.
    Gibbs, Richard A.
    Deiros, David
    Metzker, Mike
    Muzny, Donna
    Reid, Jeff
    Wheeler, David
    Wang, Jun
    Li, Jingxiang
    Jian, Min
    Li, Guoqing
    Li, Ruiqiang
    Liang, Huiqing
    Tian, Geng
    Wang, Bo
    Wang, Jian
    Wang, Wei
    Yang, Huanming
    Zhang, Xiuqing
    Zheng, Huisong
    Lander, Eric S.
    Altshuler, David L.
    Ambrogio, Lauren
    Bloom, Toby
    Cibulskis, Kristian
    Fennell, Tim J.
    Gabriel, Stacey B.
    [J]. NATURE, 2010, 467 (7319) : 1061 - 1073
  • [3] Integrating common and rare genetic variation in diverse human populations
    Altshuler, David M.
    Gibbs, Richard A.
    Peltonen, Leena
    Dermitzakis, Emmanouil
    Schaffner, Stephen F.
    Yu, Fuli
    Bonnen, Penelope E.
    de Bakker, Paul I. W.
    Deloukas, Panos
    Gabriel, Stacey B.
    Gwilliam, Rhian
    Hunt, Sarah
    Inouye, Michael
    Jia, Xiaoming
    Palotie, Aarno
    Parkin, Melissa
    Whittaker, Pamela
    Chang, Kyle
    Hawes, Alicia
    Lewis, Lora R.
    Ren, Yanru
    Wheeler, David
    Muzny, Donna Marie
    Barnes, Chris
    Darvishi, Katayoon
    Hurles, Matthew
    Korn, Joshua M.
    Kristiansson, Kati
    Lee, Charles
    McCarroll, Steven A.
    Nemesh, James
    Keinan, Alon
    Montgomery, Stephen B.
    Pollack, Samuela
    Price, Alkes L.
    Soranzo, Nicole
    Gonzaga-Jauregui, Claudia
    Anttila, Verneri
    Brodeur, Wendy
    Daly, Mark J.
    Leslie, Stephen
    McVean, Gil
    Moutsianas, Loukas
    Nguyen, Huy
    Zhang, Qingrun
    Ghori, Mohammed J. R.
    McGinnis, Ralph
    McLaren, William
    Takeuchi, Fumihiko
    Grossman, Sharon R.
    [J]. NATURE, 2010, 467 (7311) : 52 - 58
  • [4] Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
    Athanasiu, Lavinia
    Mattingsdal, Morten
    Kahler, Anna K.
    Brown, Andrew
    Gustafsson, Omar
    Agartz, Ingrid
    Giegling, Ina
    Muglia, Pierandrea
    Cichon, Sven
    Rietschel, Marcella
    Pietilainen, Olli P. H.
    Peltonen, Leena
    Bramon, Elvira
    Collier, David
    St Clair, David
    Sigurdsson, Engilbert
    Petursson, Hannes
    Rujescu, Dan
    Melle, Ingrid
    Steen, Vidar M.
    Djurovic, Srdjan
    Andreassen, Ole A.
    [J]. JOURNAL OF PSYCHIATRIC RESEARCH, 2010, 44 (12) : 748 - 753
  • [5] Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population
    Betcheva, Elitza T.
    Mushiroda, Taisei
    Takahashi, Atsushi
    Kubo, Michiaki
    Karachanak, Sena K.
    Zaharieva, Irina T.
    Vazharova, Radoslava V.
    Dimova, Ivanka I.
    Milanova, Vihra K.
    Tolev, Todor
    Kirov, George
    Owen, Michael J.
    O'Donovan, Michael C.
    Kamatani, Naoyuki
    Nakamura, Yusuke
    Toncheva, Draga I.
    [J]. JOURNAL OF HUMAN GENETICS, 2009, 54 (02) : 98 - 107
  • [6] Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders
    Brandon, NJ
    Handford, EJ
    Schurov, I
    Rain, JC
    Pelling, M
    Duran-Jimeniz, B
    Camargo, LM
    Oliver, KR
    Beher, D
    Shearman, MS
    Whiting, PJ
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 2004, 25 (01) : 42 - 55
  • [7] Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia
    Callicott, JH
    Straub, RE
    Pezawas, L
    Egan, MF
    Mattay, VS
    Hariri, AR
    Verchinski, BA
    Meyer-Lindenberg, A
    Balkissoon, R
    Kolachana, B
    Goldberg, TE
    Weinberger, DR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (24) : 8627 - 8632
  • [8] Disrupted in schizophrenia 1 interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia
    Camargo, L. M.
    Collura, V.
    Rain, J-C
    Mizuguchi, K.
    Hermjakob, H.
    Kerrien, S.
    Bonnert, T. P.
    Whiting, P. J.
    Brandon, N. J.
    [J]. MOLECULAR PSYCHIATRY, 2007, 12 (01) : 74 - 86
  • [9] Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory
    Cannon, TD
    Hennah, W
    van Erp, TGM
    Thompson, PM
    Lonnqvist, J
    Huttunen, M
    Gasperoni, T
    Tuulio-Henriksson, A
    Pirkola, T
    Toga, AW
    Kaprio, J
    Mazziotta, J
    Peltonen, L
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2005, 62 (11) : 1205 - 1213
  • [10] Cardno AG, 2000, AM J MED GENET, V97, P12, DOI 10.1002/(SICI)1096-8628(200021)97:1<12::AID-AJMG3>3.3.CO