Monoamine oxidase A gene promoter methylation and transcriptional downregulation in an offender population with antisocial personality disorder

被引:68
作者
Checknita, D. [1 ]
Maussion, G. [1 ]
Labonte, B. [2 ,3 ]
Comai, S. [4 ]
Tremblay, R. E. [5 ,6 ,7 ]
Vitaro, F. [8 ]
Turecki, N. [1 ]
Bertazzo, A. [9 ]
Gobbi, G. [4 ]
Cote, G. [10 ]
Turecki, G. [1 ]
机构
[1] McGill Univ, McGill Grp Suicide Studies, Douglas Mental Hlth Univ Inst, Montreal, PQ, Canada
[2] Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[4] McGill Univ, Dept Psychiat, Neurobiol Psychiat Unit, Montreal, PQ, Canada
[5] Univ Coll Dublin, Sch Publ Hlth Physiotherapy & Populat Sci, Dublin 2, Ireland
[6] Univ Montreal, Dept Pediat, Montreal, PQ H3C 3J7, Canada
[7] Univ Montreal, Dept Psychol, Montreal, PQ H3C 3J7, Canada
[8] Univ Montreal, Sch Psychoeduc, Montreal, PQ, Canada
[9] Univ Padua, Dept Pharmaceut Sci, Padua, Italy
[10] Univ Quebec Trois Riveres, Dept Psychol, Inst Philippe Pinel, Montreal, PQ, Canada
关键词
CHILDHOOD MALTREATMENT; AGGRESSIVE-BEHAVIOR; BRAIN-SEROTONIN; MAOA GENOTYPE; ABUSE; ENVIRONMENT; ADOLESCENCE; IMPULSIVITY; EXPRESSION; CHILDREN;
D O I
10.1192/bjp.bp.114.144964
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Antisocial personality disorder (ASPD) is characterised by elevated impulsive aggression and increased risk for criminal behaviour and incarceration. Deficient activity of the monoamine oxidase A (MAOA) gene is suggested to contribute to serotonergic system dysregulation strongly associated with impulsive aggression and antisocial criminality. Aims To elucidate the role of epigenetic processes in altered MAOA expression and serotonin regulation in a population of incarcerated offenders with ASPD compared with a healthy non-incarcerated control population. Method Participants were 86 incarcerated participants with ASPD and 73 healthy controls. MAOA promoter methylation was compared between case and control groups. We explored the functional impact of MAOA promoter methylation on gene expression in vitro and blood 5-HT levels in a subset of the case group. Results Results suggest that MAOA promoter hypermethylation is associated with ASPD and may contribute to downregulation of MAOA gene expression, as indicated by functional assays in vitro, and regression analysis with whole-blood serotonin levels in offenders with ASPD. Conclusions These results are consistent with prior literature suggesting MAOA and serotonergic dysregulation in antisocial populations. Our results offer the first evidence suggesting epigenetic mechanisms may contribute to MAOA dysregulation in antisocial offenders.
引用
收藏
页码:216 / 222
页数:7
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