Human Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health, University of Texas Health Science Center at Houston, UK.
Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, UK.
J Gerontol A Biol Sci Med Sci. 2020 Feb 14;75(3):473-480. doi: 10.1093/gerona/glz245.
Methylation levels measured at defined sites across the genome have recently been shown to be correlated with an individual's chronological age. Age acceleration, or the difference between age estimated from DNA methylation status and chronological age, has been proposed as a novel biomarker of aging. In this study, the cross-sectional association between two different measures of age acceleration and cognitive function was investigated using whole blood samples from 2,157 African American participants 47-70 years of age in the population-based Atherosclerosis Risk in Communities (ARIC) Study. Cognition was evaluated using three domain-specific tests. A significant inverse association between a 1-year increase in age acceleration calculated using a blood-based age predictor and scores on the Word Fluency Test was found using a general linear model adjusted for chronological age, gender, and years of education (β = -0.140 words; p = .001) and after adding other potential confounding variables (β = -0.104 words, p = .023). The results were replicated in 1,670 European participants in the Generation Scotland: Scottish Family Health Study (fully adjusted model: β = -0.199 words; p = .034). A significant association was also identified in a trans-ethnic meta-analysis across cohorts that included an additional 708 European American ARIC study participants (fully adjusted model: β = -0.110 words, p = .003). There were no associations found using an estimate of age acceleration derived from multiple tissues. These findings provide evidence that age acceleration is a correlate of performance on a test of verbal fluency in middle-aged adults.
甲基化水平在基因组中的特定位置上的测量,最近已经被证明与个体的实际年龄相关。年龄加速,或从 DNA 甲基化状态估计的年龄与实际年龄之间的差异,已被提议作为一种新的衰老生物标志物。在这项研究中,使用来自 2157 名年龄在 47-70 岁之间的非裔美国人群体为基础的动脉粥样硬化风险社区(ARIC)研究中的全血样本,调查了两种不同的年龄加速测量方法与认知功能之间的横断面关联。使用三个特定领域的测试评估认知功能。使用基于血液的年龄预测器计算的年龄加速增加 1 年,与单词流畅性测试的分数呈显著负相关,这是通过调整为实际年龄、性别和受教育年限的一般线性模型得出的(β=-0.140 个单词;p=0.001),并且在添加其他潜在混杂变量后(β=-0.104 个单词,p=0.023)。这些结果在苏格兰世代研究:苏格兰家庭健康研究中的 1670 名欧洲参与者中得到了复制(完全调整模型:β=-0.199 个单词;p=0.034)。在包括另外 708 名 ARIC 研究欧洲裔参与者的跨种族元分析中也发现了显著的关联(完全调整模型:β=-0.110 个单词,p=0.003)。使用源自多种组织的年龄加速估计值没有发现关联。这些发现提供了证据,表明年龄加速是中年成年人言语流畅性测试表现的相关因素。