The endophenotype concept in psychiatric genetics

被引:306
作者
Flint, Jonathan
Munafo, Marcus R.
机构
[1] Univ Bristol, Dept Expt Psychol, Bristol, Avon, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
基金
英国惠康基金;
关键词
D O I
10.1017/S0033291706008750
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
The idea that some phenotypes bear a closer relationship to the biological processes that give rise to psychiatric illness than diagnostic categories has attracted considerable interest. Much effort has been devoted to finding such endophenotypes, partly because it is believed that the genetic basis of endophenotypes will be easier to analyse than that of psychiatric disease. This belief depends in part on the assumption that the effect sizes of genetic loci contributing to endophenotypes are larger than those contributing to disease susceptibility, hence increasing the chance that genetic linkage and association tests will detect them. We examine this assumption by applying meta-analytical techniques to genetic association studies of endophenotypes. We find that the genetic effect sizes of the loci examined to date are no larger than those reported for other phenotypes. A review of the genetic architecture of traits in model organisms also provides no support for the view that the effect sizes of loci contributing to phenotypes closer to the biological basis of disease is any larger than those contributing to disease itself. While endophenotype measures may afford greater reliability, it should not be assumed that they will also demonstrate simpler genetic architecture.
引用
收藏
页码:163 / 180
页数:18
相关论文
共 150 条
[1]   Meta-analysis of association between the T102C polymorphism of the 5HT2a receptor gene and schizophrenia [J].
Abdolmaleky, HM ;
Faraone, SV ;
Glatt, SJ ;
Tsuang, MT .
SCHIZOPHRENIA RESEARCH, 2004, 67 (01) :53-62
[2]  
ADLER LE, 1982, BIOL PSYCHIAT, V17, P639
[3]   Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype [J].
Ahearn, EP ;
Speer, MC ;
Chen, YT ;
Steffens, DC ;
Cassidy, F ;
Van meter, S ;
Provenzale, JM ;
Weisler, RH ;
Krishnan, KRR .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (06) :652-658
[4]  
Alarcón M, 2003, AM J PHYS ANTHROPOL, P57
[5]   Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families [J].
Alarcón, M ;
Cantor, RM ;
Liu, JJ ;
Gilliam, TC ;
Geschwind, DH .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :60-71
[6]  
Almasy L, 2001, AM J MED GENET, V105, P42, DOI 10.1002/1096-8628(20010108)105:1<42::AID-AJMG1055>3.0.CO
[7]  
2-9
[8]  
AMADOR XF, 1995, J NEUROPSYCH CLIN N, V7, P197
[9]   Genetic structure of spatial and verbal working memory [J].
Ando, J ;
Ono, Y ;
Wright, MJ .
BEHAVIOR GENETICS, 2001, 31 (06) :615-624
[10]   Cognitive dysfunctions in parents of schizophrenic patients parallel the deficits found in patients [J].
Appels, MCM ;
Sitskoorn, MM ;
Westers, P ;
Lems, E ;
Kahn, RS .
SCHIZOPHRENIA RESEARCH, 2003, 63 (03) :285-293