Department of Psychology, Stony Brook University, Stony Brook, New York, USA.
Department of Ecology and Evolution, Stony Brook University, Stony Brook, New York, USA.
J Gerontol A Biol Sci Med Sci. 2024 Jan 1;79(1). doi: 10.1093/gerona/glad242.
DNA methylation-derived epigenetic clocks offer the opportunity to examine aspects of age acceleration (ie, the difference between an individual's biological age and chronological age), which vary among individuals and may better account for age-related changes in cognitive function than chronological age. Leveraging existing ambulatory cognitive assessments in daily life from a genetically diverse sample of 142 adults in midlife, we examined associations between 5 measures of epigenetic age acceleration and performance on tasks of processing speed and working memory. Covarying for chronological age, we used multilevel models to examine associations of epigenetic age acceleration (Horvath 1, Horvath 2, Hannum, PhenoAge, and GrimAge clocks) with both average level and variability of cognitive performance. Positive age acceleration (ie, epigenetic age greater than chronological age) was associated with poorer mean processing speed (Horvath 1 and 2) and working memory (GrimAge). Higher chronological age was also associated with poorer mean processing speed and working memory performance. Further, positive age acceleration was generally associated with greater intraindividual variability in working memory and processing speed tasks, whereas being chronologically older was associated with less intraindividual variability. Although further work is needed, our results indicate age acceleration effects have comparable or greater size as those for chronological age differences, suggesting that epigenetic age acceleration may account for additional risk and interindividual variation in cognitive performance above chronological age.
DNA 甲基化衍生的表观遗传时钟提供了一个机会,可以研究年龄加速的各个方面(即个体的生物年龄与实际年龄之间的差异),这种差异在个体之间存在差异,并且可能比实际年龄更好地解释认知功能与年龄相关的变化。利用来自中年的遗传多样化样本中现有的日常活动的动态认知评估,我们研究了 5 种表观遗传年龄加速测量值与处理速度和工作记忆任务表现之间的关联。在控制实际年龄的情况下,我们使用多层次模型来研究表观遗传年龄加速(Horvath 1、Horvath 2、Hannum、PhenoAge 和 GrimAge 时钟)与认知表现的平均水平和变异性之间的关联。正的年龄加速(即表观遗传年龄大于实际年龄)与较低的平均处理速度(Horvath 1 和 2)和工作记忆(GrimAge)相关。较高的实际年龄也与较低的平均处理速度和工作记忆表现相关。此外,正的年龄加速通常与工作记忆和处理速度任务的个体内变异性增加有关,而实际年龄较大则与个体内变异性降低有关。尽管还需要进一步的研究,但我们的结果表明,年龄加速的影响与实际年龄差异的影响相当或更大,这表明表观遗传年龄加速可能在认知表现方面,除了实际年龄之外,还可以解释更多的风险和个体间差异。