Potential Role of ADRA2A Genetic Variants in the Etiology of ADHD Comorbid With Tic Disorders

J Atten Disord. 2021 Jan;25(1):33-43. doi: 10.1177/1087054718757646. Epub 2018 Feb 27.

Abstract

Objective: To evaluate the role of the adrenergic receptor alpha-2A gene (ADRA2A) in the genetic etiology of ADHD comorbid with tic disorders (ADHD+TD). Method: Two single nucleotide polymorphisms (SNPs) of ADRA2A were genotyped and analyzed in 936 normal controls and 1,815 ADHD probands, including 1,249 trios. Approximately 16% of the ADHD probands also had a diagnosis of TD. Results: No significant association was found between ADRA2A and ADHD in general. Case-control analyses indicated different allelic and genotypic distributions of rs553668 between ADHD+TD and controls in males. Family-based association tests showed that the G allele of rs1800544, the A allele of rs553668, and the GA haplotype consisting of these two SNPs were overtransmitted in the ADHD+TD trios, especially in males. Moreover, the allelic/genotypic distribution and allelic transmission were different between ADHD+TD and ADHD without TD. Conclusion:ADRA2A may be associated with ADHD+TD, especially in males.

Keywords: ADHD; ADRA2A; TD; association.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Attention Deficit Disorder with Hyperactivity* / epidemiology
  • Attention Deficit Disorder with Hyperactivity* / genetics
  • Genotype
  • Humans
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Receptors, Adrenergic, alpha-2 / genetics
  • Tic Disorders* / epidemiology
  • Tic Disorders* / genetics

Substances

  • ADRA2A protein, human
  • Receptors, Adrenergic, alpha-2