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Association between EXOC3L2 rs597668 polymorphism and Alzheimer's disease.
Shang, Hong; Fu, Jin; Zhang, Xue-Mei; Song, Rong-Rong; Wang, Wei-Zhi.
Afiliación
  • Shang H; Department of Neurology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, China; Department of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
CNS Neurosci Ther ; 19(10): 834-9, 2013 Oct.
Article en En | MEDLINE | ID: mdl-23663385
ABSTRACT

BACKGROUND:

EXOC3L2 gene rs597668 polymorphism was identified to be significantly associated with Alzheimer's disease (AD) in Caucasian population. However, recent studies reported consistent and inconsistent results in Caucasian and Asian populations.

AIMS:

In order to assess this association, we performed a meta-analysis of rs597668 polymorphism using RevMan (v.5.1) software.

METHODS:

We searched PubMed and Google scholar databases and selected 4 independent publications, which included 16 independent studies. We conducted sensitivity analysis and evaluated the publication bias. In the end, we calculated the odds ratio (OR) using fixed effect model (Mantel-Haenszel).

RESULTS:

We observed significant association between rs597668 polymorphism and AD using allele model (P = 0.006, OR = 1.09, 95% CI 1.03-1.16) and the dominant model (P = 0.008, OR = 1.11, 95% CI 1.03-1.21). DISCUSSION AND

CONCLUSIONS:

To our knowledge, this is the first study that assesses the association between rs597668 polymorphism and AD by meta-analysis. We believe that our findings will be very useful for future genetic studies in AD.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Predisposición Genética a la Enfermedad / Proteínas de Transporte Vesicular / Estudios de Asociación Genética / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: CNS Neurosci Ther Asunto de la revista: NEUROLOGIA / TERAPEUTICA Año: 2013 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Predisposición Genética a la Enfermedad / Proteínas de Transporte Vesicular / Estudios de Asociación Genética / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: CNS Neurosci Ther Asunto de la revista: NEUROLOGIA / TERAPEUTICA Año: 2013 Tipo del documento: Article País de afiliación: China
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