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No evidence for an association between the T102C and 1438 G/A polymorphisms of the serotonin 2A receptor gene in attention deficit/hyperactivity disorder in a Turkish population.
Zoroglu, Suleyman Salih; Erdal, Mehmet Emin; Erdal, Nurten; Ozen, Sakir; Alasehirli, Belgin; Sivasli, Ercan.
Afiliação
  • Zoroglu SS; Department of Child and Adolescent Psychiatry, Faculty of Medicine, Gaziantep University, Kolejtepe Hastanesi, 27200, TR-Gaziantep, Turkey. zoroglus@hotmail.com
Neuropsychobiology ; 47(1): 17-20, 2003.
Article em En | MEDLINE | ID: mdl-12606840
Disturbances in the serotonergic neurotransmission system have been implicated in the etiology of attention deficit/hyperactivity disorder (ADHD). As the importance of genetic factors is well established, genes encoding for proteins of the serotonergic pathway are important candidates to unravel the underlying genetic contribution. We previously demonstrated that the polymorphisms of the serotonin transporter gene promoter and regions of variable number of tandem repeats were involved in the pathogenesis of ADHD. The purpose of this study was to examine the relationship between ADHD and two polymorphisms (T102C and 1438 G/A) in the 5-HT2A gene in a sample of Turkish children. Using the PCR technique, these polymorphisms were assessed in 70 patients with ADHD and in 100 healthy controls. There was no significant difference between the frequencies of the T, C, G and A alleles of both groups. No association was found between the studied polymorphisms of the 5-HT2A gene and ADHD in this sample consisting of Turkish children. Overall, our results suggest that the investigated 5-HT2A polymorphisms are not major susceptibility factors in the etiology of ADHD.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Transtorno do Deficit de Atenção com Hiperatividade / Receptores de Serotonina Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Neuropsychobiology Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Turquia País de publicação: Suíça
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Transtorno do Deficit de Atenção com Hiperatividade / Receptores de Serotonina Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Neuropsychobiology Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Turquia País de publicação: Suíça