Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study

被引:52
作者
Li, YH
Tacey, K
Doil, L
van Luchene, R
Garcia, V
Rowland, C
Schrodi, S
Leong, D
Lau, K
Catanese, J
Sninsky, J
Nowotny, P
Holmans, P
Hardy, J
Powell, J
Lovestone, S
Thal, L
Owen, M
Williams, J
Goate, A
Grupe, A [1 ]
机构
[1] Celera Diagnost, Alameda, CA USA
[2] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[3] Cardiff Univ, Coll Med, Biostat & Bioinformat Unit, Cardiff CF1 3NS, S Glam, Wales
[4] NIA, Bethesda, MD 20892 USA
[5] Kings Coll London, Inst Psychiat, Dept Neurosci, London WC2R 2LS, England
[6] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
[7] Cardiff Univ, Coll Med, Dept Psychol Med, Cardiff, S Glam, Wales
关键词
Alzheimer's disease; ATP-binding cassette A1 transporter; ABCA1; polymorphism;
D O I
10.1016/j.neulet.2004.05.047
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Genetic association of ABCA1 or the ATP-binding cassette Al transporter with late-onset Alzheimer's disease (LOAD) has recently been proposed for a haplotype comprised of three single nucleotide polymorphisms (SNPs). We have genotyped these and other ABCA1 SNPs in a LOAD case-control series of 796 individuals (419 cases versus 377 controls) collected at Washington University. While our sample series is larger and thus presumably has greater power than any of the series used to implicate ABCA1, we were unable to replicate the published association, using either single markers or multiple marker haplotypes. Further, we did not observe significant and replicated association of other ABCA1 SNPs we examined with the disease, thus these ABCA1 variants do not appear to influence the risk of LOAD in this study. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:268 / 271
页数:4
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