| Literature DB >> 24863667 |
Hongsheng Gui1, Chao Qiang Jiang2, Stacey S Cherny3, Pak Chung Sham4, Lin Xu5, Bin Liu2, Ya Li Jin2, Tong Zhu2, Wei Sen Zhang2, G Neil Thomas6, Kar Keung Cheng6, Tai Hing Lam5.
Abstract
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 ε4 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.Entities:
Keywords: ACE; APOE; Alzheimer's disease; Cognitive decline; Joint effect
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Year: 2014 PMID: 24863667 DOI: 10.1016/j.neurobiolaging.2014.04.022
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673