Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease

被引:69
作者
WavrantDeVrieze, F
PerezTur, J
Lambert, JC
Frigard, B
Pasquier, F
Delacourte, A
Amouyel, P
Hardy, J
ChartierHarlin, MC
机构
[1] INST PASTEUR, INSERM, CJF 9505, SERV SANTE PUBL & EPIDEMIOL, F-59019 LILLE, FRANCE
[2] CTR GERIATR WASQUEHAL MOLINEL, F-59444 WASQUEHAL, FRANCE
[3] CTR HOSP REG & UNIV LILLE, HOP SALENGRO, CTR MEM, NEUROL CLIN, F-59037 LILLE, FRANCE
[4] INSERM, U422, F-59045 LILLE, FRANCE
基金
美国国家卫生研究院;
关键词
late-onset Alzheimer's disease; low density lipoprotein receptor-related protein; apolipoprotein E receptor; association studies; risk factor; APOLIPOPROTEIN-E; GENE; ALLELE; POLYMORPHISM; BINDING; RISK;
D O I
10.1016/S0304-3940(97)00304-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is the most common neurodegenerative disorder affecting elderly people. It usually occurs after 65 years old (late-onset AD). The epsilon 4 allele of apolipoprotein E (APOE) gene is a risk factor which contributes about 50% of the genetic risk for this form of the disease. The low density lipoprotein receptor-related protein (LRP) is a major receptor for APOE which is found in the senile plaques of AD brains. This makes it a good candidate gene for the disease. There is a polymorphism in the region upstream of the LRP gene that has been associated with AD in an American population. We examined this polymorphism by restriction fragment length polymorphism analysis in a French population with sporadic late-onset AD. In the previous report, a significant increase of the 87 bp allele was found in the AD cases; however, in our population, we observed a significant decrease with this same allele of the LRP gene. The possible reasons for this discrepancy, linkage disequilibrium or statistical anomaly, are discussed. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:68 / 70
页数:3
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