Evaluating historical candidate genes for schizophrenia

被引:216
作者
Farrell, M. S. [1 ]
Werge, T. [2 ,3 ,4 ]
Sklar, P. [5 ,6 ,7 ]
Owen, M. J. [8 ,9 ]
Ophoff, R. A. [10 ,11 ,12 ]
O'Donovan, M. C. [8 ,9 ]
Corvin, A. [13 ]
Cichon, S. [14 ,15 ,16 ]
Sullivan, P. F. [1 ,17 ,18 ]
机构
[1] Univ N Carolina, Ctr Psychiat Genom, Dept Genet, Genom Med, Chapel Hill, NC 27599 USA
[2] Mental Hlth Serv Copenhagen, Inst Biol Psychiat, MHC Sct Hans, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Clin Med, Aarhus, Denmark
[4] Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark
[5] Icahn Sch Med Mt Sinai, Dept Psychiat, Div Psychiat Genom, New York, NY 10029 USA
[6] Icahn Sch Med Mt Sinai, Inst Multiscale Biol, New York, NY 10029 USA
[7] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[8] Cardiff Univ, Sch Med, Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci,MRC, Cardiff CF10 3AX, S Glam, Wales
[9] Cardiff Univ, Natl Ctr Mental Hlth, Cardiff CF10 3AX, S Glam, Wales
[10] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Ctr Neurobehav Genet, Los Angeles, CA 90024 USA
[11] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[12] Univ Med Ctr Utrecht, Brain Ctr Rudolf Magnus, Dept Psychiat, Utrecht, Netherlands
[13] Trinity Coll Dublin, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin, Ireland
[14] Univ Basel, Div Med Genet, Dept Biomed, Basel, Switzerland
[15] Univ Bonn, Inst Human Genet, Bonn, Germany
[16] Life & Brain Ctr, Dept Genom, Bonn, Germany
[17] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[18] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27599 USA
关键词
GENOME-WIDE ASSOCIATION; COPY NUMBER VARIATION; BIPOLAR DISORDER; COMMON VARIANTS; RISK-FACTOR; SYSTEMATIC METAANALYSES; NO ASSOCIATION; RECEPTOR GENE; SUSCEPTIBILITY; POLYMORPHISM;
D O I
10.1038/mp.2015.16
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Prior to the genome-wide association era, candidate gene studies were a major approach in schizophrenia genetics. In this invited review, we consider the current status of 25 historical candidate genes for schizophrenia (for example, COMT, DISC1, DTNBP1 and NRG1). The initial study for 24 of these genes explicitly evaluated common variant hypotheses about schizophrenia. Our evaluation included a meta-analysis of the candidate gene literature, incorporation of the results of the largest genomic study yet published for schizophrenia, ratings from informed researchers who have published on these genes, and ratings from 24 schizophrenia geneticists. On the basis of current empirical evidence and mostly consensual assessments of informed opinion, it appears that the historical candidate gene literature did not yield clear insights into the genetic basis of schizophrenia. A likely reason why historical candidate gene studies did not achieve their primary aims is inadequate statistical power. However, the considerable efforts embodied in these early studies unquestionably set the stage for current successes in genomic approaches to schizophrenia.
引用
收藏
页码:555 / 562
页数:8
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