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Genetic association of sirtuin genes and Parkinson's disease.
Jesús, Silvia; Gómez-Garre, Pilar; Carrillo, Fátima; Cáceres-Redondo, María T; Huertas-Fernández, Ismael; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Vargas-González, Laura; Carballo, Manuel; Mir, Pablo.
Afiliação
  • Jesús S; Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla/Instituto de Biomedicina de Sevilla, Av. Manuel Siurot s/n, 41013 Seville, Spain.
J Neurol ; 260(9): 2237-41, 2013 Sep.
Article em En | MEDLINE | ID: mdl-23719790
ABSTRACT
Parkinson's disease (PD) is a neurodegenerative disease caused by both genetic and environmental factors. Sirtuins are highly-conserved, NAD-dependent class III deacetylases that regulate a variety of cellular functions. Most of the known sirtuins have been involved in animal models of neurodegenerative disorders, such as PD. Although seven sirtuin family members have been identified (SIRT1-SIRT7) the relationship between sirtuins and PD in humans has not been established. Our aim was to investigate the association between sirtuin genes and risk of PD. We included 326 PD patients and 371 controls from southern Spain. Forty-one single nucleotide polymorphisms (SNPs) in sirtuin genes were genotyped in order to determine whether they were related to the risk of PD. These SNPs included Tag-SNPs, coding non-synonymous SNPs and SNPs affecting activity of microRNA binding sites. No relationship was found between these SNPs in sirtuin genes and PD. Our data indicate that variations in sirtuin genes do not affect the risk for PD, at least in our population.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Sirtuínas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: J Neurol Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Sirtuínas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: J Neurol Ano de publicação: 2013 Tipo de documento: Article