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Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population

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机构: [a]Department of Neurology and Neurobiology, Key Laboratory of Neurodegenerative Diseases for Ministry of Education, Beijing Institute of Geriatrics and Xuanwu Hospital of Capital University of Medical Sciences, 100053 Beijing, China [b]Department of Neurology, Peking Union Hospital, Chinese Academy of Medical Science and Peking Union Medical College, 100730 Beijing, China [c]Institute of Mental Health, West China Hospital, Sichuan University, 610065 Chengdu Sichuan, China [d]Department of Neurology, The First Affiliated Hospital, Xi’an Jiaotong University, 710049 Xi’an Shanxi, China [e]Institute of Neurology, Huashan Hospital, Fudan University, 200040 Shanghai, China
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关键词: Alzheimer's disease low-density lipoprotein receptor-related protein polymorphism

摘要:
Alzheimer's disease (AD) is the most common neurodegenerative disorders in the elderly. Low-density lipoprotein receptor-related protein (LRP), as a receptor of apolipoprotein E (APOE), APP, and alpha2 macroglobulin (alpha 2-M), keeps the balance between degeneration and production of beta-amyloid protein (A beta) clearance. Its gene had been defined as a candidate gene for AD, but the results were not universal. Total 496 AD patients and 478 controls were recruited in Chinese Han population and real-time PCR was used to detect the polymorphism of LRP C766T. Multiple logistic regression, Chi-square test and survival analysis were performed to explore the association. The distribution of LRP genotypes and alleles was significantly different between cases and controls, and T allele could reduce the risk for developing AD (OR of CT genotype: 0.57; 95% CI: 0.38-0.85, rho=0.003; OR of T allele: 0.57; 95% CI: 0.39-0.83, rho=0.003). TT genotype carriers had 5 years later for developing AD compared with CC genotype carriers, but survival analysis did not conform this (LRP TT vs. CT and CC log rank chi(2)=2.71, rho=0.26). The distribution of LRP C766T genotypes and alleles was different among different severity stratified by MMSE yet (rho=0.26). Our data suggested that the polymorphism of LRP C766T was strongly associated with AD and T allele might be a protective factor for AD in Chinese Han population. Crown Copyright (C) 2008 Published by Elsevier Ireland Ltd. All rights reserved.

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基金编号: M10641450002-07N4145-00210

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出版当年[2007]版:
大类 | 3 区 医学
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 神经科学
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出版当年[2006]版:
Q3 NEUROSCIENCES
最新[2023]版:
Q3 NEUROSCIENCES

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第一作者机构: [a]Department of Neurology and Neurobiology, Key Laboratory of Neurodegenerative Diseases for Ministry of Education, Beijing Institute of Geriatrics and Xuanwu Hospital of Capital University of Medical Sciences, 100053 Beijing, China
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通讯机构: [b]Department of Neurology, Peking Union Hospital, Chinese Academy of Medical Science and Peking Union Medical College, 100730 Beijing, China
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