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本文引用的文献

1
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.全基因组关联研究确定了CLU和CR1基因中与阿尔茨海默病相关的变异。
Nat Genet. 2009 Oct;41(10):1094-9. doi: 10.1038/ng.439. Epub 2009 Sep 6.
2
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.全基因组关联研究确定了与阿尔茨海默病相关的CLU和PICALM基因变体。
Nat Genet. 2009 Oct;41(10):1088-93. doi: 10.1038/ng.440. Epub 2009 Sep 6.
3
APOE-4 genotype and neurophysiological vulnerability to Alzheimer's and cognitive aging.APOE-4基因分型与阿尔茨海默病及认知衰老的神经生理易感性
Annu Rev Clin Psychol. 2009;5:343-62. doi: 10.1146/annurev.clinpsy.032408.153625.
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Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.阿尔茨海默病遗传关联研究的系统荟萃分析:AlzGene数据库
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Apolipoprotein E and cognitive performance: a meta-analysis.载脂蛋白E与认知表现:一项荟萃分析。
Psychol Aging. 2004 Dec;19(4):592-600. doi: 10.1037/0882-7974.19.4.592.
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Predictors of mortality in 2,249 nonagenarians--the Danish 1905-Cohort Survey.2249名九旬老人的死亡预测因素——丹麦1905年队列研究
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The heritability of level and rate-of-change in cognitive functioning in Danish twins aged 70 years and older.70岁及以上丹麦双胞胎认知功能水平及变化率的遗传度。
Exp Aging Res. 2002 Oct-Dec;28(4):435-51. doi: 10.1080/03610730290080416.
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The heritability of cognitive functioning in very old adults: evidence from Danish twins aged 75 years and older.高龄成年人认知功能的遗传度:来自75岁及以上丹麦双胞胎的证据。
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Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.早发型常染色体显性阿尔茨海默病:患病率、遗传异质性及突变谱
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CLU 和 PICALM 基因的遗传变异与最年长老年人的认知功能有关。

Genetic variations in the CLU and PICALM genes are associated with cognitive function in the oldest old.

机构信息

The Danish Aging Research Center, Epidemiology Unit, Institute of Public Health, University of Southern Denmark, Odense, Denmark.

出版信息

Neurobiol Aging. 2011 Mar;32(3):554.e7-11. doi: 10.1016/j.neurobiolaging.2010.07.016. Epub 2010 Aug 23.

DOI:10.1016/j.neurobiolaging.2010.07.016
PMID:20739100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3042035/
Abstract

Recently, two large, and independent genome wide association studies of late-onset Alzheimer's disease (AD) established association with the same rs11136000 variation in the clusterin (CLU) gene. In addition, one variation, rs3851179, in the phosphatidylinositol binding clathrin assembly protein (PICALM) gene and one variation, rs6656401, in the complement component (3b/4b) receptor 1 (CR) gene were associated with AD. Here, we replicate these associations with cognitive functioning in 1380 individuals from the Danish (1905) birth cohort study of the oldest old (92-93 years at intake) using measures of Mini Mental State Examination (MMSE) and a cognitive composite score. We found a significant association between the highly frequent CLU rs11136000 T allele (38%) and better performance on the cognitive composite score (p = 0.016) explaining 0.5% of the mean variation in cognitive composite score, and for men a significant association between the highly frequent PICALM rs3851179 A allele (38%). Better performance was found (p = 0.024), explaining 1.4% of the mean variation in cognitive composite score in men. These alleles correspond to the minor alleles initially found more frequent in controls than in cases of AD.

摘要

最近,两项针对晚发性阿尔茨海默病(AD)的大型、独立全基因组关联研究在聚类素(CLU)基因中的相同 rs11136000 变异与 AD 建立了关联。此外,载脂蛋白(PI)结合网格蛋白装配蛋白(PICALM)基因中的 rs3851179 变异和补体成分(3b/4b)受体 1(CR)基因中的 rs6656401 变异与 AD 相关。在这里,我们使用 Mini Mental State Examination(MMSE)和认知综合评分在来自丹麦(1905 年)最年长(入组时 92-93 岁)的出生队列研究的 1380 名个体中复制了这些与认知功能的关联。我们发现 CLU 基因 rs11136000 高度频繁的 T 等位基因(38%)与认知综合评分的更好表现之间存在显著关联(p=0.016),解释了认知综合评分中 0.5%的平均变异,并且对于男性,PICALM 基因 rs3851179 高度频繁的 A 等位基因(38%)之间存在显著关联。发现表现更好(p=0.024),解释了男性认知综合评分中 1.4%的平均变异。这些等位基因对应于最初在 AD 病例中比在对照中更频繁出现的次要等位基因。