MAOA genotype, family relations and sexual abuse in relation to adolescent alcohol consumptionShow others and affiliations
2011 (English)In: Addiction Biology, ISSN 1355-6215, E-ISSN 1369-1600, Vol. 16, no 2, p. 347-355Article in journal (Refereed) Published
Abstract [en]
The aim of the present study was to investigate MAOA gene-environment (G*E) interactions in relation to adolescent alcohol consumption. In the county of Vastmanland, Sweden, all 17-18-year-old students were asked to complete an anonymous questionnaire and provide a saliva sample during class hours. A total of 2263 students completed the questionnaire (77.4%) and a saliva sample was provided by 2131 participants. Failed MAOA u-variable number of tandem repeats (VNTR) genotype analyses and internal non-responses left 851 boys and 735 girls (total n = 1586) to be investigated. Alcohol use disorder identification test was used to measure hazardous alcohol consumption. MAOA u-VNTR was used to measure biological risk in interaction with poor family relations and experience of sexual abuse. The model was also adjusted for non-independent socioeconomic variables, separated parents, type of housing and parental unemployment. Results showed that the MAOA u-VNTR, in interaction with psychosocial risk factors, such as the quality of family relations and sexual abuse, was related to high alcohol consumption among adolescents. Girls, carrying the long MAOA u-VNTR variant showed a higher risk of being high alcohol consumers, whereas among boys, the short allele was related to higher alcohol consumption. The present study supports the hypothesis that there is a relation between MAOA u-VNTR and alcohol consumption and that this relation is modulated by environmental factors. Furthermore, the present study also supports the hypothesis that there is a sex difference in the G*E interaction.
Place, publisher, year, edition, pages
WILEY-BLACKWELL , 2011. Vol. 16, no 2, p. 347-355
Keywords [en]
Abuse, adolescent, alcohol, environment, gene, MAOA
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:mdh:diva-52035DOI: 10.1111/j.1369-1600.2010.00238.xISI: 000288024800015PubMedID: 20731636Scopus ID: 2-s2.0-79952504211OAI: oai:DiVA.org:mdh-52035DiVA, id: diva2:1484380
2020-10-282020-10-282021-01-20Bibliographically approved