Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior

被引:85
作者
Wakschlag, L. S. [1 ]
Kistner, E. O. [2 ]
Pine, D. S. [3 ]
Biesecker, G. [1 ]
Pickett, K. E. [4 ]
Skol, A. D. [5 ]
Dukic, V. [2 ]
Blair, R. J. R. [3 ]
Leventhal, B. L. [1 ]
Cox, N. J. [5 ]
Burns, J. L. [1 ]
Kasza, K. E. [2 ]
Wright, R. J. [6 ]
Cook, E. H., Jr. [1 ]
机构
[1] Univ Illinois, Dept Psychiat, Inst Juvenile Res, Chicago, IL 60608 USA
[2] Univ Chicago, Dept Hlth Studies, Chicago, IL 60637 USA
[3] NIMH, Lab Affect & Dev Neurosci, Intramural Res Program, Bethesda, MD 20892 USA
[4] Univ York, Dept Hlth Sci, York YO10 5DD, N Yorkshire, England
[5] Univ Chicago, Dept Med, Med Genet Sect, Chicago, IL 60637 USA
[6] Harvard Univ, Sch Med, Channing Lab, Boston, MA 02115 USA
关键词
prenatal smoking; MAOA; gene x environment interaction; developmental psychopathology; DEFICIT HYPERACTIVITY DISORDER; DOPAMINE TRANSPORTER GENOTYPE; GENE-ENVIRONMENT INTERACTION; MATERNAL SMOKING; MONOAMINE-OXIDASE; FUNCTIONAL POLYMORPHISM; EXTERNALIZING PROBLEMS; INDIVIDUAL-DIFFERENCES; PREGNANCY; RISK;
D O I
10.1038/mp.2009.22
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
Genetic susceptibility to antisocial behavior may increase fetal sensitivity to prenatal exposure to cigarette smoke. Testing putative gene x exposure mechanisms requires precise measurement of exposure and outcomes. We tested whether a functional polymorphism in the gene encoding the enzyme monoamine oxidase A (MAOA) interacts with exposure to predict pathways to adolescent antisocial behavior. We assessed both clinical and information-processing outcomes. One hundred seventy-six adolescents and their mothers participated in a follow-up of a pregnancy cohort with well-characterized exposure. A sex-specific pattern of gene x exposure interaction was detected. Exposed boys with the low-activity MAOA 5' uVNTR (untranslated region variable number of tandem repeats) genotype were at increased risk for conduct disorder (CD) symptoms. In contrast, exposed girls with the high-activity MAOA uVNTR genotype were at increased risk for both CD symptoms and hostile attribution bias on a face-processing task. There was no evidence of a gene-environment correlation (rGE). Findings suggest that the MAOA uVNTR genotype, prenatal exposure to cigarettes and sex interact to predict antisocial behavior and related information-processing patterns. Future research to replicate and extend these findings should focus on elucidating how gene x exposure interactions may shape behavior through associated changes in brain function. Molecular Psychiatry (2010) 15, 928-937; doi:10.1038/mp.2009.22; published online 3 March 2009
引用
收藏
页码:928 / 937
页数:10
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