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Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease.
Morgan, A R; Hamilton, G; Turic, D; Jehu, L; Harold, D; Abraham, R; Hollingworth, P; Moskvina, V; Brayne, C; Rubinsztein, D C; Lynch, A; Lawlor, B; Gill, M; O'Donovan, M; Powell, J; Lovestone, S; Williams, J; Owen, M J.
Afiliação
  • Morgan AR; Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK. morganar1@cardiff.ac.uk
Am J Med Genet B Neuropsychiatr Genet ; 147B(6): 727-31, 2008 Sep 05.
Article em En | MEDLINE | ID: mdl-18163421
ABSTRACT
Late-onset Alzheimer's disease (LOAD) is a genetically complex neurodegenerative disorder. Currently, only the epsilon4 allele of the Apolipoprotein E gene has been identified unequivocally as a genetic susceptibility factor for LOAD. Others remain to be found. In 2002 we observed genome-wide significant evidence of linkage to a region on chromosome 10q11.23-q21.3 [Myers et al. (2002) Am J Med Genet 114235-244]. Our objective in this study was to test every gene within the maximum LOD-1 linkage region, for association with LOAD. We obtained results for 528 SNPs from 67 genes, with an average density of 1 SNP every 10 kb within the genes. We demonstrated nominally significant association with LOAD for 4 SNPs rs1881747 near DKK1 (P = 0.011, OR = 1.24), rs2279420 in ANK3 (P = 0.022, OR = 0.79), rs2306402 in CTNNA3 (P = 0.024, OR = 1.18), and rs5030882 in CXXC6 (P = 0.046, OR = 1.29) in 1,160 cases and 1,389 controls. These results would not survive correction for multiple testing but warrant attempts at confirmation in independent samples.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 10 / Polimorfismo de Nucleotídeo Único / Doença de Alzheimer Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 10 / Polimorfismo de Nucleotídeo Único / Doença de Alzheimer Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2008 Tipo de documento: Article