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Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with
Anita Thapar1, Kate Langley, Tom Fowler
1Department of Psychological Medicine, College of Medicine, School of Psychology, Cardiff University, Heath Park, Cardiff, Wales. thapar@cardiff.ac.uk
Insights
A specific catechol O-methyltransferase (COMT) gene variant and lower birth weight predict early-onset antisocial behavior. The val/val genotype increases susceptibility to prenatal risks, highlighting gene-environment interactions.
Area of Science:
- Neuroscience
- Genetics
- Developmental Psychology
Background:
- Early-onset antisocial behavior (ASB) with attention-deficit/hyperactivity disorder (ADHD) is a severe variant with poor outcomes.
- Identifying early predictors is crucial for intervention.
- Prefrontal cortical function, influenced by the COMT gene variant, is implicated.
Purpose of the Study:
- To test if the COMT gene variant predicts early-onset ASB in a high-risk sample.
- To examine the effects of birth weight (a prenatal adversity index) on ASB.
- To investigate genotype x birth weight interactions.
Main Methods:
- A family-based genetic study conducted from 1997-2003 in the UK.
- Prospective recruitment of 240 clinic children diagnosed with ADHD or hyperkinetic disorder.
- Standardized assessments of ASB, IQ, and DSM-IV conduct disorder symptoms.
Main Results:
- Significant main effects for the COMT gene variant (P = .002).
- Significant main effects for birth weight (P = .002).
- A significant gene x environment interaction (COMT x birth weight) was observed (P = .006).
Conclusions:
- The COMT gene variant and birth weight predict early-onset ASB in high-risk children.
- Individuals with the val/val genotype are more vulnerable to prenatal risks (lower birth weight).
- This highlights the interplay between genetic predisposition and environmental factors in ASB development.
Context:
Early-onset antisocial behavior accompanied by attention-deficit/hyperactivity disorder is a clinically severe variant of antisocial behavior that is associated with a particularly poor outcome. Identifying early predictors is thus important. Genetic and prenatal environmental risk factors and prefrontal cortical function are thought to contribute. Recent evidence suggests that prefrontal cortical function is influenced by a valine/methionine variant in the catechol O-methyltransferase (COMT) gene.
Objective:
To test the a priori hypothesis that this genetic variant predicts early-onset antisocial behavior in a high-risk sample and further examine the effects of birth weight, an environmentally influenced index of prenatal adversity previously linked to childhood disruptive behaviors and genotype x birth weight interaction.
Design, Setting, And Participants:
A family-based genetic study was undertaken between 1997 and 2003. Participants were prospectively recruited from child and adolescent psychiatry and child health clinics in the United Kingdom and included 240 clinic children who met diagnostic criteria for attention-deficit/hyperactivity disorder or hyperkinetic disorder. Participants underwent comprehensive standardized assessments including measures of antisocial behavior and IQ. Main Outcome Measure DSM-IV symptoms of childhood-onset conduct disorder rated by trained interviewers using a standard diagnostic interview.
Results:
The results show main effects of the COMT gene variant (P = .002), birth weight (P = .002), and a significant gene x environment (COMT x birth weight) interaction (P = .006).
Conclusions:
Early-onset antisocial behavior in a high-risk clinical group is predicted by a specific COMT gene variant previously linked with prefrontal cortical function and birth weight, and those possessing the val/val genotype are more susceptible to the adverse effects of prenatal risk as indexed by lower birth weight.
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