Early life stress, MAOA, and gene-environment interactions predict behavioral disinhibition in children

Genes Brain Behav. 2010 Feb;9(1):65-74. doi: 10.1111/j.1601-183X.2009.00535.x. Epub 2009 Sep 9.

Abstract

Several, but not all, studies have shown that the monoamine oxidase A functional promoter polymorphism (MAOA-LPR) interacts with childhood adversity to predict adolescent and adult antisocial behavior. However, it is not known whether MAOA-LPR interacts with early life (pre-birth-3 years) stressors to influence behavior in prepubertal children. The Avon Longitudinal Study of Parents and Children, UK, is a community-representative cohort study of children followed from pre-birth onwards. The impact of family adversity from pre-birth to age 3 years and stressful life events from 6 months to 7 years on behavioral disinhibition was determined in 7500 girls and boys. Behavioral disinhibition measures were: mother-reported hyperactivity and conduct disturbances (Strengths and Difficulties Questionnaire) at ages 4 and 7 years. In both sexes, exposure to family adversity and stressful life events in the first 3 years of life predicted behavioral disinhibition at age 4, persisting until age 7. In girls, MAOA-LPR interacted with stressful life events experienced from 6 months to 3.5 years to influence hyperactivity at ages 4 and 7. In boys, the interaction of MAOA-LPR with stressful life events between 1.5 and 2.5 years predicted hyperactivity at age 7 years. The low activity MAOA-LPR variant was associated with increased hyperactivity in girls and boys exposed to high stress. In contrast, there was no MAOA-LPR interaction with family adversity. In a general population sample of prepubertal children, exposure to common stressors from pre-birth to 3 years predicted behavioral disinhibition, and MAOA-LPR- stressful life event interactions specifically predicted hyperactivity.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antisocial Personality Disorder / etiology*
  • Child
  • Child Behavior*
  • Child, Preschool
  • Cohort Studies
  • Conduct Disorder / etiology*
  • Environment*
  • Female
  • Fetus
  • Genotype
  • Humans
  • Hyperkinesis / etiology*
  • Infant
  • Infant, Newborn
  • Longitudinal Studies
  • Male
  • Monoamine Oxidase / genetics*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic
  • Sex Factors
  • Stress, Psychological*

Substances

  • Monoamine Oxidase