Chapuis Julien, Moisan Frédéric, Mellick Georges, Elbaz Alexis, Silburn Peter, Pasquier Florence, Hannequin Didier, Lendon Corinne, Campion Dominique, Amouyel Philippe, Lambert Jean-Charles
Inserm, U744, Institut Pasteur de Lille, Université de Lille 2, Lille, France.
Hum Mol Genet. 2008 Sep 15;17(18):2863-7. doi: 10.1093/hmg/ddn183. Epub 2008 Jun 25.
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.
阿尔茨海默病(AD)和帕金森病(PD)是老年人中最常见的两种神经退行性疾病,据推测它们有共同的遗传决定因素。最近,李等人提出NEDD9基因中的一个变体可能是这些共同遗传因素之一。我们试图通过进行病理和样本量方面的等效分析来证实这一初步观察结果。我们在三项独立的AD病例对照研究(n = 3176)和两项独立的PD病例对照研究(n = 1855)中对NEDD9 rs760678单核苷酸多态性进行了基因分型。然而,在这些人群中,我们均未检测到该单核苷酸多态性与患AD或PD风险之间存在关联。总之,这些数据表明NEDD9基因的rs760678单核苷酸多态性充其量只是AD或PD的一个弱遗传决定因素。