no evidence for association between norepinephrine transporter-3081 (a/t) polymorphism and attention deficit hyperactivity disorder in iranian population

conclusions the results of the study show no significant association between norepinephrine transporter polymorphism scl6a2 and adhd. results the percentages of adhd subtypes for combined, inattentive, and hyperactive/impulsive were 72.2%, 17.2%, and 11.9%, respectively. there was no significant association between norepinephrine transporter polymorphism and adhd (p = 0.81). moreover, no significant relationship was found between gender [male (p = 0.92) and female (p = 0.63)] and polymorphism. no significant association was found between subtypes of adhd [combined (p = 0.46), inattentive (p = 0.41), hyperactive/impulsive (p = 0.32)] and polymorphism scl6a2. this lack of association can also be seen in gender in every subtype. objectives the current study was conducted to investigate the association between norepinephrine transporter-3081 (a/t) polymorphisms and adhd in iranian population. patients and methods participants were chosen from children and adolescents diagnosed with adhd referred to imam hoseyn hospital. a child and adolescent psychiatrist confirmed the diagnosis using the kiddie-sads-present and lifetime version (k-sads-pl) semi-structural interview. the control group was from pupils of schools in tehran (capital city of iran) who had no history or presence of psychiatric and medical complications. also, a child and adolescent psychiatrist confirmed their health using the k-sads-pl semi-structural interview. genetic examinations were dna distraction, polymerase chain reaction (pcr), and restricted fragment length polymorphism (rflp), which were conducted according to standard protocols. the statistical analysis was performed using chi-square and fisher's exact test in spss version 21. background attention deficit hyperactivity disorder (adhd) can lead to drastic problems for the patient and its worldwide prevalence is 5%-12%. it also has many comorbidities with other disorders, and the genetic contribution seems the most significant cause.