The Danish Aging Research Center, Epidemiology Unit, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
Neurobiol Aging. 2011 Mar;32(3):554.e7-11. doi: 10.1016/j.neurobiolaging.2010.07.016. Epub 2010 Aug 23.
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.
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。