Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: Longitudinal evidence of a gene X environment interaction

被引:837
作者
Caspi, A
Moffitt, TE
Cannon, M
McClay, J
Murray, R
Harrington, H
Taylor, A
Arseneault, L
Williams, B
Braithwaite, A
Poulton, R
Craig, IW
机构
[1] Kings Coll London, Inst Psychiat, SGDP Ctr, London SE5 8AF, England
[2] Univ Wisconsin, Dept Psychol, Madison, WI 53706 USA
[3] Kings Coll London, Inst Psychiat, Dept Psychol Med, London SE5 8AF, England
[4] Royal Coll Surgeons Ireland, Dept Psychiat, Dublin 2, Ireland
[5] Univ Otago, Dunedin Sch Med, Dunedin, New Zealand
基金
英国医学研究理事会; 英国经济与社会研究理事会;
关键词
cannabis; catechol-O-methyltransferase; gene-environment interaction; psychosis;
D O I
10.1016/j.biopsych.2005.01.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recent evidence documents that cannabis use by young people is a modest statistical risk factor for psychotic symptoms in adulthood, such as hallucinations and delusions, as well as clinically significant schizophrenia. The vast majority of cannabis users do not develop psychosis, however, prompting its to hypothesize that some people are genetically vulnerable to the deleterious effects of cannabis. Methods: In a longitudinal study of a representative birth cohort followed to adulthood, we tested why cannabis use is associated with the emergence of psychosis in a minority of users, but not in others. Results: A functional polymorphism in the catechol-O-methyltransferase (COMT) gene moderated the influence of adolescent cannabis use on developing adult psychosis. Carriers of the COMT valine(158) allele were most likely to exhibit psychotic symptoms and to develop schizophreniform disorder if they used cannabis. Cannabis use bad no such adverse influence on individuals with two copies of the methionine allele. Conclusions: These findings provide evidence of a gene X environment interaction and suggest that a role of some susceptibility genes is to influence vulnerability to environmental pathogens.
引用
收藏
页码:1117 / 1127
页数:11
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