TY - JOUR PY - 2017// TI - Associations of multiple trauma types and MAOA with severe aggressive behavior and MAOA effects on training outcome JO - European Neuropsychopharmacology A1 - Smeijers, Danique A1 - Bulten, Erik A1 - Franke, Barbara A1 - Buitelaar, Jan A1 - Verkes, Robbert-Jan SP - ePub EP - ePub VL - ePub IS - ePub N2 - Previous research showed that the disposition to react with disproportionate aggression in adults is influenced by an interaction between a variant in the X-chromosomal monoamine oxidase A gene (MAOA) and early traumatic events. Such studies have often focused on a single type of trauma, whereas we know that experiencing multiple trauma types is associated with more detrimental consequences. The differential susceptibility hypothesis suggests that individuals who are most susceptible to adversity, are also most likely to benefit from supportive experiences in childhood. Differences in susceptibility are thought to be partly genetically driven. In the present study we explored whether a genotype of MAOA linked to lower expression of the gene (MAOA-L) modified the effect of multiple types of trauma on aggression and/or altered responsiveness to treatment among adults with severe aggression. Forensic psychiatric outpatients (FPOs) (N=150) receiving treatment for aggression regulation problems were recruited. Traumatic events and aggression were measured using self-report. FPOs with multiple trauma types and those with the MAOA-L allele reported more severe levels of aggression. No interaction effects between MAOA genotype and trauma emerged. There were no differences in response to the intervention between FPOs with and without the MAOA-L variant, whereas FPOs with a single type of trauma showed the slowest reduction of aggression. FPOs with multiple types of trauma reported the highest levels of aggression over the course of treatment. Future research is needed to elucidate this association in further detail. The current study emphasized the importance of early recognition of early traumatic events.

Copyright © 2017 Elsevier B.V. and ECNP. All rights reserved.

Language: en

LA - en SN - 0924-977X UR - http://dx.doi.org/10.1016/j.euroneuro.2017.06.016 ID - ref1 ER -