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COMT val158met is not associated with Aβ-amyloid and APOE ε4 related cognitive decline in cognitively normal older adults

机译:在认知正常的成年人中COMT val158met与Aβ-淀粉样蛋白和APOEε4相关的认知能力下降无关

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摘要

The non-synonymous single nucleotide polymorphism (SNP), Val158Met within the Catechol-O-methyltransferase (COMT) gene has been associated with altered levels of cognition and memory performance in cognitively normal adults. This study aimed to investigate the independent and interactional effects of COMT Val158Met on cognitive performance. In particular, it was hypothesised that COMT Val158Met would modify the effect of neocortical Aβ-amyloid (Aβ) accumulation and carriage of the apolipoprotein E (APOE) ε4 allele on cognition in preclinical Alzheimer’s disease (AD). In 598 cognitively normal older adults with known neocortical Aβ levels, linear mixed modelling revealed no significant independent or interactional associations between COMT Val158Met and cognitive decline. These findings do not support previous associations between COMT Val158Met and cognitive performance and suggest this variant does not influence Aβ-amyloid or APOE ε4 driven cognitive decline in a well characterised cohort of cognitively normal older adults.
机译:儿茶酚-O-甲基转移酶(COMT)基因中的非同义单核苷酸多态性(SNP)Val158Met已与认知正常成年人的认知水平和记忆能力改变有关。这项研究旨在调查COMT Val158Met对认知表现的独立和交互作用。特别是,有人假设COMT Val158Met将改变新皮质Aβ-淀粉样蛋白(Aβ)的积聚和载脂蛋白E(APOE)ε4等位基因对临床前阿尔茨海默氏病(AD)认知的影响。在598名已知新皮质Aβ水平的认知正常的成年人中,线性混合模型显示COMT Val158Met与认知能力下降之间没有显着的独立或相互作用联系。这些发现不支持COMT Val158Met与认知能力之间的先前关联,并且表明该变异体不影响Aβ-淀粉样蛋白或APOEε4驱动的认知正常老年人群中认知功能的下降。

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