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SIRT2 polymorphism rs10410544 is associated with Alzheimer's disease in a Han Chinese population.
Xia, Man; Yu, Jin-Tai; Miao, Dan; Lu, Rui-Chun; Zheng, Xue-Ping; Tan, Lan.
Afiliación
  • Xia M; Department of Neurology, Qingdao Municipal Hospital, WeiFang Medical University, China.
  • Yu JT; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China; Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, China. Electronic address: yu-jintai@163.com.
  • Miao D; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China.
  • Lu RC; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China.
  • Zheng XP; Department of Neurology, The Affiliated Hospital of the Medical College of Qingdao University, Qingdao, China. Electronic address: simplexueping@163.com.
  • Tan L; Department of Neurology, Qingdao Municipal Hospital, WeiFang Medical University, China; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China; Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, China. Electronic address: dr.t
J Neurol Sci ; 336(1-2): 48-51, 2014 Jan 15.
Article en En | MEDLINE | ID: mdl-24139700
ABSTRACT
Sirtuin 2 (SIRT2) is a strong protein deacetylase, which is highly expressed in central nervous system. Recently, an association between SIRT2 rs10410544 polymorphism and late-onset Alzheimer's disease (LOAD) was found in the APOEε4-negative Caucasian population. To investigate the potential association between the rs10410544 C/T polymorphism of SIRT2 and the risk of LOAD, we conducted an independent replication case-control study in a Northern Han Chinese population comprising 1133 cases and 1159 healthy controls being matched for age and gender. The results revealed that there were significant differences in genotype and allele frequencies between LOAD cases and controls (genotype P=0.008, allele P=0.009). When compared with the C allele, the T allele of rs10410544 demonstrated a 1.709-fold risk for developing LOAD. After stratification by apolipoprotein E (APOE) ε4-carrying status, only APOEε4 noncarriers (P=0.035, adjusted OR=1.656, 95% CI 1.036-2.647) showed the relation between LOAD and SIRT2 rs10410544 T allele. This study provides the evidence that the rs10410544 C/T polymorphism of SIRT2 was associated with genetic susceptibility to LOAD in a Northern Han Chinese population.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo Genético / Vigilancia de la Población / Pueblo Asiatico / Sirtuina 2 / Estudios de Asociación Genética / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Screening_studies Límite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: J Neurol Sci Año: 2014 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo Genético / Vigilancia de la Población / Pueblo Asiatico / Sirtuina 2 / Estudios de Asociación Genética / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Screening_studies Límite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: J Neurol Sci Año: 2014 Tipo del documento: Article País de afiliación: China