Options
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease
File(s)
File | Description | Size | Format | |
---|---|---|---|---|
Li_2008.pdf | 593.3 KB |
Author(s)
Date Issued
26 November 2007
Date Available
20T13:54:43Z June 2013
Abstract
Late-onset Alzheimer's disease (LOAD) and Parkinson's disease (PD) are the most common neurodegenerative disorders and in both diseases susceptibility is known to be influenced by genes. We set out to identify novel susceptibility genes for LOAD by performing a large scale, multi-tiered association study testing 4692 single nucleotide polymorphism (SNPs). We identified a SNP within a putative transcription factor binding site in the NEDD9 gene (neural precursor cell expressed, developmentally down-regulated), that shows good evidence of association with disease risk in four out of five LOAD samples [N = 3521, P = 5.38x10(-6), odds ratio (OR) = 1.38 (1.20-1.59)] and in addition, we observed a similar pattern of association in two PD sample sets [N = 1464, P = 0.0145, OR =1.31 (1.05-1.62)]. In exploring a potential mechanism for the association, we observed that expression of NEDD9 and APOE show a strong inverse correlation in the hippocampus of Alzheimer's cases. These data implicate NEDD9 as a novel susceptibility gene for LOAD and possibly PD.
Type of Material
Journal Article
Publisher
Oxford University Press
Journal
Human Molecular Genetics
Volume
17
Issue
5
Start Page
759
End Page
767
Copyright (Published Version)
2007 The Author(s)
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
Owning collection
Scopus© citations
36
Acquisition Date
Feb 5, 2023
Feb 5, 2023
Views
1715
Last Week
1
1
Last Month
3
3
Acquisition Date
Feb 6, 2023
Feb 6, 2023
Downloads
270
Last Month
87
87
Acquisition Date
Feb 6, 2023
Feb 6, 2023