Department of Epidemiology, Harvard T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts, USA.
Weill Cornell Medical College, New York, New York, USA.
J Gerontol A Biol Sci Med Sci. 2024 Aug 1;79(8). doi: 10.1093/gerona/glae167.
The association between cardiometabolic risk factors and cognitive function has been well documented, but the underlying mechanisms are not fully understood. This longitudinal study aimed to investigate the potential mediating role of DNA methylation in this association. We conducted the analyses in 3 708 participants (mean [standard deviation {SD}] age: 67.3 [9.5], women: 57.9%) from the Health and Retirement Study who were assessed in the 2014-2020 waves, had Infinium Methylation EPIC BeadChip methylation assays from the 2016 Venous Blood Study, and had cognitive assessment between 2016 and 2020. Causal mediation analyses were used to test the mediation role of DNA methylation in the associations between cardiometabolic risk factors and cognition, adjusting for demographic, socioeconomic, and lifestyle factors. Hypertension (-0.061 in composite cognitive z-score; 95% confidence interval [CI: -0.119, -0.004]) and diabetes (-0.134; 95% CI: [-0.198, -0.071]) were significantly associated with worse cognitive function while abnormal body weight and hypercholesterolemia were not. An increased number of cardiometabolic risk factors was associated with worse cognitive function (p = .002). DNA methylation significantly mediated the association of hypertension (mediated effect on composite cognitive z-score: -0.023; 95% CI: -0.033, -0.014), diabetes (-0.022; 95% CI: -0.032, -0.014), and obesity (-0.021; 95% CI: -0.033, -0.011) with cognitive function, whereas the mediation effect was not observed for having hypercholesterolemia. The estimated proportions mediated were 37.4% for hypertension and 16.7% for diabetes. DNA methylation may be an important mediator linking cardiometabolic risk factors to worse cognition and might even provide a potential target for dementia prevention.
心血管代谢风险因素与认知功能之间的关系已得到充分证实,但潜在机制尚不完全清楚。本纵向研究旨在探讨 DNA 甲基化在此关联中的潜在中介作用。我们对来自健康与退休研究的 3708 名参与者(平均[标准差]年龄:67.3[9.5],女性:57.9%)进行了分析,这些参与者在 2014 年至 2020 年期间接受了评估,在 2016 年静脉血研究中进行了 Infinium 甲基化 EPIC BeadChip 甲基化检测,并在 2016 年至 2020 年期间进行了认知评估。因果中介分析用于测试 DNA 甲基化在心血管代谢风险因素与认知之间的关联中的中介作用,调整了人口统计学、社会经济和生活方式因素。高血压(复合认知 z 评分降低 0.061;95%置信区间[CI]:-0.119,-0.004)和糖尿病(-0.134;95%CI:-0.198,-0.071)与认知功能较差显著相关,而异常体重和高胆固醇血症则没有。心血管代谢风险因素的数量增加与认知功能较差相关(p=0.002)。DNA 甲基化显著介导了高血压(对复合认知 z 评分的中介作用:-0.023;95%CI:-0.033,-0.014)、糖尿病(-0.022;95%CI:-0.032,-0.014)和肥胖(-0.021;95%CI:-0.033,-0.011)与认知功能的关联,而对于高胆固醇血症,中介效应则不明显。估计的中介比例分别为高血压的 37.4%和糖尿病的 16.7%。DNA 甲基化可能是将心血管代谢风险因素与认知功能下降联系起来的一个重要中介,甚至可能为预防痴呆症提供一个潜在的目标。