Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder

Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral pathology characterized by distinct degrees of inattention, hyperactivity and impulsivity. Although ADHD etiology remains elusive, the ADRA2A candidate gene underlies a particular interest, since it participates in the prefr...

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Autores:
Tipo de recurso:
Fecha de publicación:
2013
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22657
Acceso en línea:
https://doi.org/10.1007/s10072-013-1569-4
https://repository.urosario.edu.co/handle/10336/22657
Palabra clave:
Alpha 2A adrenergic receptor
Alpha 2a adrenergic receptor gene
Article
Attention deficit disorder
Child
Colombia
Controlled study
Female
Gene
Gene sequence
Genetic code
Genetic variability
Human
Major clinical study
Male
Promoter region
School child
Sequence analysis
Single nucleotide polymorphism
Wild type
Attention Deficit Disorder with Hyperactivity
Child
Colombia
Female
Humans
Male
ADHD
ADRA2A
Attention deficit hyperactivity disorder
Behavior
Genetics
Single Nucleotide
DNA
Adrenergic
alpha-2
Polymorphism
Receptors
Sequence Analysis
Rights
License
Abierto (Texto Completo)
Description
Summary:Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral pathology characterized by distinct degrees of inattention, hyperactivity and impulsivity. Although ADHD etiology remains elusive, the ADRA2A candidate gene underlies a particular interest, since it participates in the prefrontal cortex regulation of executive function. Three SNPs located on 5? and 3?UTR regions of the gene have been extensively explored but none of them have been definitely validated as a predisposition or a causative sequence variation. In this study, in order to determine whether ADRA2A non-synonymous sequence variants, resulting in biochemical modifications of the protein, are a common cause of the disease we sequenced the complete ADRA2A coding region in a panel of ADHD children of Colombian origin. We identified the c.1138 C>A (p.Arg380Arg) silent substitution. We conclude that ADRA2A non-synonymous sequence variants do not cause ADHD in our sample population. We cannot formerly discard a potential role of this gene during ADHD pathogenesis since only the coding region was analysed. We hope that these results will encourage further researchers to sequence the promoter and coding regions of ADRA2A in large panels of ADHD patients from distinct ethnical origins. © 2013 Springer-Verlag Italia.