https://www.mdu.se/

mdu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Good parent-child relationship protects against alcohol use in maltreated adolescent females carrying the MAOA-uVNTR susceptibility allele
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden. Centre for Clinical Research, Uppsala University, Västerås, Sweden.
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden. Centre for Clinical Research, Uppsala University, Västerås, Sweden. Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden. Centre for Clinical Research, Uppsala University, Västerås, Sweden.
Centre for Clinical Research, Uppsala University, Västerås, Sweden. Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden.
Show others and affiliations
2024 (English)In: Frontiers in Psychiatry, E-ISSN 1664-0640, Vol. 15, article id 1375363Article in journal (Refereed) Published
Abstract [en]

Introduction: Risk-allele carriers of a Monoamine oxidase A (MAOA) gene, short-allele (MAOA-S) in males and long-allele (MAOA-L) in females, in the presence of a negative environment, are associated with alcohol misuse. Whether MAOA-S/L alleles also present susceptibility to a positive environment to mitigate the risk of alcohol misuse is unknown. Thus, we assessed the association of the three-way interaction of MAOA, maltreatment, and positive parent-child relationship with alcohol consumption among adolescents. Methods: This prospective study included 1416 adolescents (females: 59.88%) aged 16 ̵ 19 years from Sweden, enrolled in the “Survey of Adolescent Life in Västmanland” in 2012. Adolescents self-reported alcohol consumption, maltreatment by a family (FM) or non-family member (NFM), parent-child relationship, and left saliva for MAOA genotyping. Results and discussion: We observed sex-dependent results. Females carrying MAOA-L with FM or NFM and a good parent-child relationship reported lower alcohol consumption than those with an average or poor parent-child relationship. In males, the interactions were not significant. Results suggest MAOA-L in females, conventionally regarded as a “risk”, is a “plasticity” allele as it is differentially susceptible to negative and positive environments. Results highlight the importance of a good parent-child relationship in mitigating the risk of alcohol misuse in maltreated individuals carrying genetic risk. However, the interactions were not significant after adjusting to several environmental and behavioural covariates, especially parent’s alcohol use, negative parent-child relationship, and nicotine use (smoking and/or snus), suggesting predictor and outcome intersection. Future studies and frameworks for preventive strategies should consider these covariates together with alcohol consumption. More studies with larger sample sizes are needed to replicate the findings.

Place, publisher, year, edition, pages
Frontiers Media SA , 2024. Vol. 15, article id 1375363
Keywords [en]
adolescents, alcohol, candidate gene, differential susceptibility, gene-environment interactions (GxE), maltreatment, monoamine oxidase A (MAOA) gene, parent-child relationship, amine oxidase (flavin containing) isoenzyme A, genomic DNA, adolescent, adult, alcohol consumption, allele, Article, child abuse, child parent relation, cohort analysis, conceptual framework, DNA polymorphism, emotional abuse, environment, female, gene, genetic risk, genetics, genotype, genotyping, heredity, human, human experiment, major clinical study, male, mental disease, plasticity, principal component analysis, questionnaire, saliva, sample size, self report, susceptibility allele
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:mdh:diva-68166DOI: 10.3389/fpsyt.2024.1375363ISI: 001283805300001Scopus ID: 2-s2.0-85200212828OAI: oai:DiVA.org:mdh-68166DiVA, id: diva2:1889016
Available from: 2024-08-14 Created: 2024-08-14 Last updated: 2025-10-10Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopus

Authority records

Nilsson, Kent W.

Search in DiVA

By author/editor
Nilsson, Kent W.
By organisation
Health and Welfare
In the same journal
Frontiers in Psychiatry
Clinical Medicine

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 242 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf