Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder

Am J Med Genet. 2000 Jun 12;96(3):293-301. doi: 10.1002/1096-8628(20000612)96:3<293::aid-ajmg12>3.0.co;2-c.

Abstract

This study utilized a sample of 313 eight- to sixteen-year-old same-sex twin pairs (183 monozygotic, 130 dizygotic) to assess the etiology of comorbidity between reading disability (RD) and attention-deficit/hyperactivity disorder (ADHD). RD was assessed by a discriminant function score based on the Peabody Individual Achievement Test, a standardized measure of academic achievement. The DSM-III version of the Diagnostic Interview for Children and Adolescents was used to assess symptoms of ADHD, and separate factor scores were computed for inattention and hyperactivity/impulsivity (hyp/imp). Individuals with RD were significantly more likely than individuals without RD to exhibit elevations on both symptom dimensions, but the difference was larger for inattention than hyp/imp. Behavior genetic analyses indicated that the bivariate heritability of RD and inattention was significant (h(2)(g(RD/Inatt)) = 0.39), whereas the bivariate heritability of RD and hyp/imp was minimal and nonsignificant (h(2)(g(RD/Hyp)) = 0.05). Approximately 95% of the phenotypic covariance between RD and symptoms of inattention was attributable to common genetic influences, whereas only 21% of the phenotypic overlap between RD and hyp/imp was due to the same genetic factors.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.
  • Twin Study

MeSH terms

  • Adolescent
  • Attention Deficit Disorder with Hyperactivity / complications*
  • Attention Deficit Disorder with Hyperactivity / genetics
  • Child
  • Comorbidity
  • Diseases in Twins*
  • Dyslexia / complications*
  • Dyslexia / genetics
  • Female
  • Genotype
  • Humans
  • Male
  • Regression Analysis
  • Statistics as Topic
  • Twins, Dizygotic
  • Twins, Monozygotic