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Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease

Identifieur interne : 008698 ( Main/Exploration ); précédent : 008697; suivant : 008699

Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease

Auteurs : Julien Chapuis [France] ; Frédéric Moisan [France] ; Georges Mellick [Australie] ; Alexis Elbaz [France] ; Peter Silburn [Australie] ; Florence Pasquier [France] ; Didier Hannequin [France] ; Corinne Lendon [Australie] ; Dominique Campion [France] ; Philippe Amouyel [France] ; Jean-Charles Lambert [France]

Source :

RBID : ISTEX:A41BD80097BCF3CF1F839BFB926EC2C53657A76E

Descripteurs français

English descriptors

Abstract

Alzheimer's disease (AD) and Parkinson's disease (PD), the two most common neurodegenerative disorders in the elderly, have been hypothesized to share genetic determinants. Recently, Li et al. proposed that a variant in the NEDD9 gene may be one of these common genetic factors. We attempted to confirm this initial observation by conducting an equivalent analysis in terms of pathologies and sample size. We genotyped the NEDD9 rs760678 SNP in three independent AD case–control studies (n = 3176) and two independent PD case–control studies (n = 1855). However, we failed to detect an association of this SNP with the risk of developing AD or PD, in any of these populations. In conclusion, these data indicate that the rs760678 SNP of the NEDD9 gene is at best a weak genetic determinant of AD or PD.

Url:
DOI: 10.1093/hmg/ddn183


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<div type="abstract">Alzheimer's disease (AD) and Parkinson's disease (PD), the two most common neurodegenerative disorders in the elderly, have been hypothesized to share genetic determinants. Recently, Li et al. proposed that a variant in the NEDD9 gene may be one of these common genetic factors. We attempted to confirm this initial observation by conducting an equivalent analysis in terms of pathologies and sample size. We genotyped the NEDD9 rs760678 SNP in three independent AD case–control studies (n = 3176) and two independent PD case–control studies (n = 1855). However, we failed to detect an association of this SNP with the risk of developing AD or PD, in any of these populations. In conclusion, these data indicate that the rs760678 SNP of the NEDD9 gene is at best a weak genetic determinant of AD or PD.</div>
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