Common genetic variation and performance on standardized cognitive tests

被引:76
作者
Cirulli, Elizabeth T. [1 ]
Kasperaviciute, Dalia [1 ,2 ]
Attix, Deborah K. [3 ,4 ]
Need, Anna C. [1 ]
Ge, Dongliang [1 ]
Gibson, Greg [5 ]
Goldstein, David B. [1 ]
机构
[1] Duke Univ, Duke Inst Genome Sci & Policy, Ctr Human Genome Variat, Durham, NC 27708 USA
[2] UCL Inst Neurol, Dept Clin & Expt Epilepsy, London, England
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27708 USA
[4] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC 27708 USA
[5] Georgia Inst Technol, Sch Biol, Ctr Integrat Genom, Atlanta, GA 30332 USA
关键词
endophenotypes; genome-wide association; cognition; psychiatric conditions; common variants; GENOME-WIDE ASSOCIATION; NEUROPSYCHOLOGICAL ENDOPHENOTYPES; MEMORY PERFORMANCE; EPISODIC MEMORY; POLYMORPHISM; SCHIZOPHRENIA; TRAITS; INTELLIGENCE; RELATIVES; SIBLINGS;
D O I
10.1038/ejhg.2010.2
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
One surprising feature of the recently completed waves of genome-wide association studies is the limited impact of common genetic variation in individually detectable polymorphisms on many human traits. This has been particularly pronounced for studies on psychiatric conditions, which have failed to produce clear, replicable associations for common variants. One popular explanation for these negative findings is that many of these traits may be genetically heterogeneous, leading to the idea that relevant endophenotypes may be more genetically tractable. Aspects of cognition may be the most important endophenotypes for psychiatric conditions such as schizophrenia, leading many researchers to pursue large-scale studies on the genetic contributors of cognitive performance in the normal population as a surrogate for aspects of liability to disease. Here, we perform a genome-wide association study with two tests of executive function, Digit Symbol and Stroop Color-Word, in 1086 healthy volunteers and with an expanded cognitive battery in 514 of these volunteers. We show that, consistent with published studies of the psychiatric conditions themselves, no single common variant has a large effect (explaining >4-8% of the population variation) on the performance of healthy individuals on standardized cognitive tests. Given that these are important endophenotypes, our work is consistent with the idea that identifying rare genetic causes of psychiatric conditions may be more important for future research than identifying genetically homogenous endophenotypes. European Journal of Human Genetics (2010) 18, 815-820; doi: 10.1038/ejhg.2010.2; published online 3 February 2010
引用
收藏
页码:815 / 819
页数:5
相关论文
共 58 条
[1]  
ALTSHULER D, 2008, COMMUNICATION
[2]  
[Anonymous], 1978, PSYCHOL ASSESSMENT R
[3]   Neurocognitive endophenotypes (Endophenocognitypes) from studies of relatives of bipolar disorder subjects: A systematic review [J].
Balanza-Martinez, Vicent ;
Rubio, Cristina ;
Selva-Vera, Gabriel ;
Martinez-Aran, Anabel ;
Sanchez-Moreno, Jose ;
Salazar-Fraile, Jose ;
Vieta, Eduard ;
Tabares-Seisdedos, Rafael .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2008, 32 (08) :1426-1438
[4]   Working memory in siblings of schizophrenia patients [J].
Barrantes-Vidal, Neus ;
Aguilera, Mari ;
Campanera, Silvia ;
Fatjo-Vilas, Mar ;
Guitart, Marc ;
Miret, Salvador ;
Valero, Sergi ;
Fananas, Lourdes .
SCHIZOPHRENIA RESEARCH, 2007, 95 (1-3) :70-75
[5]  
Beck A.T., 1993, BECK DEPRESSION INVE
[6]   Testing for neuropsychological endophenotypes in siblings discordant for attention-deficit/hyperactivity disorder [J].
Bidwell, L. Cinnamon ;
Willcutt, Erik G. ;
DeFries, John C. ;
Pennington, Bruce F. .
BIOLOGICAL PSYCHIATRY, 2007, 62 (09) :991-998
[7]   Neurocognitive correlates of the COMT Val 158Met polymorphism in chronic schizophrenia [J].
Bilder, RM ;
Volavka, J ;
Czobor, P ;
Malhotra, AK ;
Kennedy, JL ;
Ni, XQ ;
Goldman, RS ;
Hoptman, MJ ;
Sheitman, B ;
Lindenmayer, JP ;
Citrome, L ;
McEvoy, JP ;
Kunz, M ;
Chakos, M ;
Cooper, TB ;
Lieberman, JA .
BIOLOGICAL PSYCHIATRY, 2002, 52 (07) :701-707
[8]   Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].
Burton, Paul R. ;
Clayton, David G. ;
Cardon, Lon R. ;
Craddock, Nick ;
Deloukas, Panos ;
Duncanson, Audrey ;
Kwiatkowski, Dominic P. ;
McCarthy, Mark I. ;
Ouwehand, Willem H. ;
Samani, Nilesh J. ;
Todd, John A. ;
Donnelly, Peter ;
Barrett, Jeffrey C. ;
Davison, Dan ;
Easton, Doug ;
Evans, David ;
Leung, Hin-Tak ;
Marchini, Jonathan L. ;
Morris, Andrew P. ;
Spencer, Chris C. A. ;
Tobin, Martin D. ;
Attwood, Antony P. ;
Boorman, James P. ;
Cant, Barbara ;
Everson, Ursula ;
Hussey, Judith M. ;
Jolley, Jennifer D. ;
Knight, Alexandra S. ;
Koch, Kerstin ;
Meech, Elizabeth ;
Nutland, Sarah ;
Prowse, Christopher V. ;
Stevens, Helen E. ;
Taylor, Niall C. ;
Walters, Graham R. ;
Walker, Neil M. ;
Watkins, Nicholas A. ;
Winzer, Thilo ;
Jones, Richard W. ;
McArdle, Wendy L. ;
Ring, Susan M. ;
Strachan, David P. ;
Pembrey, Marcus ;
Breen, Gerome ;
St Clair, David ;
Caesar, Sian ;
Gordon-Smith, Katherine ;
Jones, Lisa ;
Fraser, Christine ;
Green, Elain K. .
NATURE, 2007, 447 (7145) :661-678
[9]  
Butcher LM, 2008, GENES BRAIN BEHAV, V7, P435, DOI 10.1111/j.1601-183X.2007.00368.x
[10]   Cognitive traits link to human chromosomal regions [J].
Buyske, S ;
Bates, ME ;
Gharani, N ;
Matise, TC ;
Tischfield, JA ;
Manowitz, P .
BEHAVIOR GENETICS, 2006, 36 (01) :65-76