IntroductionSymptoms of hyperactivity/impulsivity and inattention are dimensionally distributed in the population. Evidence supporting this idea comes from the study of twin pairs from the general population, which demonstrate high heritability estimates for these behavioural traits, ranging from 0.60 to 0.91. [1][2][3] The low end of the distribution would be represented by few behavioural problems and better cognitive function than the high and symptomatic end. This extreme and impairing end would probably be represented by the categorical diagnosis of attention-deficit/hyperactivity disorder (ADHD).4 A study on inhibition, an executive function whose impairments are part of the cognitive deficits seen in individuals with ADHD, demonstrated that performance on inhibition-related tasks were positively associated with ADHD-like traits in a large sample of healthy adults who did not have a first-degree relative with ADHD.
5The heritability estimates for ADHD are essentially the same for both continuous and categorical approaches, consistent with a dimensional view of ADHD and a strong genetic component. [1][2][3]6 Based on the normal distribution of ADHD traits in the general population, the identification and understanding of ADHD susceptibility genes may bene fit from studies of this dimensional characteristic of ADHD in nonclinical samples.2 Despite high heritability estimates, the identification of ADHD genetic susceptibility markers has been difficult, with few replicable findings described so far. 7,8 The main candidates for ADHD molecular genetic studies have been genes involved in the dopamine pathway, given considerable evidence supporting the dopaminergic hypothesis. According to this theory, an Background: Attention-deficit/hyperactivity disorder (ADHD) symptoms are dimensionally distributed in the population. This study aimed to assess the role of the catechol-O-methyltransferase (COMT) and of the dopamine transporter (DAT1) genes on ADHD symptoms in the general population. Methods: We investigated 4101 individuals from the 1993 Pelotas Birth Cohort Study using the parent version of the Strengths and Difficulties Questionnaire (SDQ) at ages 11 and 15 years. The SDQ hyperactivity/inattention scores were the main outcomes. Results: Linear regression analyses demonstrated that the increasing number of COMT 158 Val and DAT1 10R alleles significantly predicted increasing SDQ hyperactivity/inattention scores in boys at both 11 and 15 years of age (β coefficient = 0.049, t = 2.189, p = 0.029, R 2 = 0.012, and β coefficient = 0.064, t = 2.832, p = 0.005, R 2 = 0.008, respectively). The presence of both COMT 158 Val and DAT1 10R alleles was also associated with full categorical ADHD diagnosis at 18 years of age in boys (χ 2 = 4.561, p = 0.033, odds ratio 2.473, 95% confidence interval 1.048-5.838) from this cohort. We did not observe these associations in girls. Limitations: Our analyses of SDQ hyperactivity/inattention scores were not corrected for SDQ scores of conduct problems because these variables were h...