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Published on: August 4, 2022
Oxytocin Receptor Gene Variant Interacts with Intervention Delivery Format in Predicting Intervention Outcomes for
Andrea L Glenn1, John E Lochman2, Thomas Dishion3
1Center for the Prevention of Youth Behavior Problems, Department of Psychology, The University of Alabama, P.O. Box 870348, Tuscaloosa, AL, 35487, USA. alglenn1@ua.edu.
Genetic risk influences treatment for aggressive youth. Children with a specific oxytocin receptor gene (OXTR) variant benefited more from individual therapy, while others improved regardless of format.
Area of Science:
- Child Psychology
- Behavioral Genetics
- Neuroscience
Background:
- Coping Power is an evidence-based program for aggressive youth, typically group-delivered.
- Concerns exist about potential negative effects of grouping high-risk youth.
- Genetic factors may influence how individuals respond to different intervention formats.
Purpose of the Study:
- To investigate if genetic risk moderates the outcome of group versus individual Coping Power interventions.
- To examine the role of the oxytocin receptor gene (OXTR) variant rs2268493 in intervention response.
Main Methods:
- 197 fourth-grade African-American children were randomly assigned to Group or Individual Coping Power.
- The OXTR rs2268493 variant was genotyped.
- Longitudinal behavior assessments were collected over 1 year.
- Growth curve analyses examined genotype by delivery format interactions.
Main Results:
- A significant genotype by delivery format interaction was found.
- Youth with the A/A genotype improved regardless of intervention format.
- Carriers of the G allele showed improvement only in the individual format; they worsened in the group format.
Conclusions:
- Genetic factors, specifically OXTR rs2268493, can predict individual response to intervention format.
- Youth with the G allele may be more susceptible to negative peer influences in group settings.
- Personalized intervention strategies based on genetic profiles may enhance treatment efficacy for aggressive behavior.
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