Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms

被引:8
|
作者
Orlacchio, A
Kawarai, T
Polidoro, M
Stefani, A
Orlacchio, A
St George-Hyslop, PH
Bernardi, G
机构
[1] IRCCS Santa Lucia, Neurogenet Lab, I-00179 Rome, Italy
[2] Univ Roma Tor Vergata, Policlin Tor Vergata Neurol, Dipartimento Neurosci, I-00133 Rome, Italy
[3] Univ Toronto, Tanz Neurosci Bldg, Ctr Res Neurodegenerat, Toronto, ON M5S 3H2, Canada
[4] Toronto Hosp, Dept Med Neurol, Toronto, ON M5T 2S8, Canada
[5] Univ Perugia, Dipartimento Sci Biochim & Biotecnol Molecolari, I-06126 Perugia, Italy
关键词
Alzheimer's disease; single nucleotide polymorphisms; Nicastrin gene;
D O I
10.1016/S0304-3940(02)01022-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The biological study of the Nicastrin protein shows its crucial role in the pathogenesis of Alzheimer's disease (AD). We tested the hypothesis that the Nicastrin (NCSTN) gene might be genetically associated with AD. The association analysis of two single nucleotide polymorphisms (SNPs) in the coding region (cSNPs) of NCSTN were performed in an Italian population. No evidence of association was obtained between the two SNPs investigated in sporadic and familial AD cases under the stratification of currently known genetic risk factors including the apolipoprotein E (APOE), the presenilins and the beta-amyloid precursor protein. The result suggests no apparent synergic interaction between the NCSTN and APOE epsilon4 in the risk to develop the late onset sporadic form of AD. But considering its biological effects, the result can not exclude the NCSTN as candidate for genetic factor in AD. Further genetic study of the NCSTN would be necessary to evaluate the potential genetic involvement in AD. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:115 / 118
页数:4
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