A gene × gene interaction between DRD2 and DRD4 is associated with conduct disorder and antisocial behavior in males
2007

Gene Interaction Linked to Conduct Disorder in Males

Sample size: 872 publication Evidence: moderate

Author Information

Author(s): Kevin M Beaver, John Paul Wright, Matt DeLisi, Anthony Walsh, Michael G Vaughn, Danielle Boisvert, Jamie Vaske

Primary Institution: College of Criminology and Criminal Justice, Florida State University

Hypothesis

Is there a gene × gene interaction between DRD2 and DRD4 associated with conduct disorder and antisocial behavior in males?

Conclusion

A gene × gene interaction between DRD2 and DRD4 is associated with the development of conduct disorder and adult antisocial behavior in males.

Supporting Evidence

  • DRD2 and DRD4 did not have significant independent effects on conduct disorder.
  • The interaction between DRD2 and DRD4 was a statistically significant predictor of conduct problems.
  • Individuals possessing the A-1 allele and the 7R allele are significantly more likely to develop conduct problems in adolescence.

Takeaway

This study found that two specific genes work together to increase the chances of boys having behavior problems like fighting and being mean.

Methodology

The study used multivariate regression analysis on self-report questionnaires and DNA genotyping from a sample of 872 male participants.

Potential Biases

The sample may not be representative of all American males as only a subsample provided DNA for genotyping.

Limitations

The study did not include clinical diagnoses of conduct disorder and relied on self-reported measures, which may not capture all forms of antisocial behavior.

Participant Demographics

The sample consisted of male participants, including both African American and non-Hispanic Caucasian males.

Statistical Information

P-Value

p=0.030 for the interaction between DRD2 and DRD4 predicting conduct problems.

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1744-9081-3-30

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication