首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population.
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Genetic association between low-density lipoprotein receptor-related protein gene polymorphisms and Alzheimer's disease in Chinese Han population.

机译:低密度脂蛋白受体相关蛋白基因多态性与中国汉族人群阿尔茨海默氏病之间的遗传关联。

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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 (alpha2-M), keeps the balance between degeneration and production of beta-amyloid protein (Abeta) 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.
机译:阿尔茨海默氏病(AD)是老年人中最常见的神经退行性疾病。低密度脂蛋白受体相关蛋白(LRP)作为载脂蛋白E(APOE),APP和alpha2巨球蛋白(alpha2-M)的受体,在变性和β-淀粉样蛋白(Abeta)清除产生之间保持平衡。它的基因已被定义为AD的候选基因,但结果并不普遍。在中国汉族人群中招募了496名AD患者和478名对照,并使用实时PCR检测LRP C766T的多态性。进行多元逻辑回归,卡方检验和生存分析以探讨这种关联。 LRP基因型和等位基因的分布在病例和对照组之间存在显着差异,T等位基因可以降低发生AD的风险(CT基因型的OR:0.57; 95%CI:0.38-0.85,rho = 0.003; T等位基因的OR: 0.57; 95%CI:0.39-0.83,rho = 0.003)。与CC基因型携带者相比,TT基因型携带者发展AD的时间要晚5年,但生存分析与之不符(LRP TT对CT和CC log rank chi(2)= 2.71,rho = 0.26)。 LRP C766T基因型和等位基因的分布在MMSE分层的不同严重程度之间仍存在差异(rho = 0.26)。我们的数据表明,LRP C766T的多态性与AD密切相关,T等位基因可能是中国汉族人群AD的保护因素。

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