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- Publisher
- Wiley
- Copyright
- Copyright © 2007 Wiley‐Liss, Inc.
- ISSN
- 1552-4841
- eISSN
- 1552-485X
- DOI
- 10.1002/ajmg.b.30670
- pmid
- 18163421
- Publisher site
- See Article on Publisher Site
Abstract
Late‐onset Alzheimer's disease (LOAD) is a genetically complex neurodegenerative disorder. Currently, only the ε4 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 114:235–244). 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. © 2007 Wiley‐Liss, Inc.
Journal
American Journal of Medical Genetics part B – Wiley
Published: Sep 5, 2008