| NEUROBIOLOGY OF AGING | 卷:35 |
| Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study | |
| Article | |
| Gui, Hongsheng1  Jiang, Chao Qiang2  Cherny, Stacey S.1,3,4  Sham, Pak Chung1,3  Xu, Lin5  Liu, Bin2  Jin, Ya Li2  Zhu, Tong2  Zhang, Wei Sen2  Thomas, G. Neil6  Cheng, Kar Keung6  Tai Hing Lam5  | |
| [1] Univ Hong Kong, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China | |
| [2] Guangzhou 12 Hosp, Guangzhou, Guangdong, Peoples R China | |
| [3] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Hong Kong, Hong Kong, Peoples R China | |
| [4] Univ Hong Kong, LKS Fac Med, Ctr Genom Sci, Hong Kong, Hong Kong, Peoples R China | |
| [5] Univ Hong Kong, Sch Publ Hlth, Hong Kong, Hong Kong, Peoples R China | |
| [6] Univ Birmingham, Dept Publ Hlth Epidemiol & Biostat, Birmingham, W Midlands, England | |
| 关键词: Cognitive decline; Alzheimer's disease; ACE; APOE; Joint effect; | |
| DOI : 10.1016/j.neurobiolaging.2014.04.022 | |
| 来源: Elsevier | |
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【 摘 要 】
Cognitive decline is a reduction in cognitive ability usually associated with aging, and those with more extreme cognitive decline either have or are at risk of progressing to mild cognitive impairment and dementia including Alzheimer's disease (AD). We hypothesized that genetic variants predisposing to AD should be predictive of cognitive decline in elderly individuals. We selected 1325 subjects with extreme cognitive decline and 1083 well-matched control subjects from the Guangzhou Biobank Cohort Study in which more than 30,000 southern Chinese older people have been recruited and followed up. Thirty single-nucleotide polymorphisms in 29 AD-associated genes were genotyped. No statistically significant allelic associations with cognitive decline were found by individual variant analysis. At the level of genotypic association, we confirmed that the APOE epsilon 4 homozygote significantly accelerated cognitive decline and found that carriers of the ACE rs1800764_C allele were more likely to show cognitive decline than noncarriers, particularly in those without college education. However, these effects do not survive after multiple testing corrections, and together they only explain 1.7% of the phenotypic variance in cognitive score change. This study suggests that AD risk variants and/or genes are not powerful predictors of cognitive decline in our Chinese sample. (C) 2014 Elsevier Inc. All rights reserved.
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| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_neurobiolaging_2014_04_022.pdf | 292KB |
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