The monoamine oxidase A (MAO-A) gene, family function and maltreatment as predictors of destructive behaviour during male adolescent alcohol consumptionShow others and affiliations
2007 (English)In: Addiction, ISSN 0965-2140, E-ISSN 1360-0443, Vol. 102, no 3, p. 389-398Article in journal (Refereed) Published
Abstract [en]
Aim To investigate possible interactions between a polymorphism in the monoamine oxidase A (MAO-A) gene promoter, family relations and maltreatment/ sexual abuse on adolescent alcohol-related problem behaviour among male adolescents. Design, setting and participants A cross-sectional study of a randomized sample of 66 male individuals from a total population of 16- and 19-year adolescents from a Swedish county. Boys, who volunteered to participate answering an alcohol-related problem/ behaviour questionnaire, were investigated with regard to interactions between such problems, family function, maltreatment and MAO-A genotype. Measurements MAO-A genotype, family relations history, history of being maltreated or abused and alcohol-related problem behaviour. Findings Boys with the short (three-repeat) variant of the MAO-A gene, who had been maltreated/abused or came from families with poor relations, showed significantly higher scores of alcohol-related problems. We also found that maltreatment/ abuse independently showed the strongest relation to alcohol-related problems among boys in our model. Conclusions The results suggest that both maltreatment and MAO-A genotype may be useful for the understanding of male adolescent alcohol-related problem behaviour.
Place, publisher, year, edition, pages
Uppsala Univ, Cent Hosp Vasteras, Clin Res Ctr, Vasteras, Sweden. Uppsala Univ, Pharmacol Unit, Dept Neurosci, Uppsala, Sweden.: WILEY , 2007. Vol. 102, no 3, p. 389-398
Keywords [en]
adolescent, alcohol drinking, behaviour, environment, genes, juvenile delinquency, risk-taking
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:mdh:diva-52058DOI: 10.1111/j.1360-0443.2006.01702.xISI: 000244098000010PubMedID: 17298646Scopus ID: 2-s2.0-33846897384OAI: oai:DiVA.org:mdh-52058DiVA, id: diva2:1484352
2020-10-282020-10-282021-01-20Bibliographically approved