Edwards Travyse A, Zhai Tianhua, Nho Kwangsik, Saykin Andrew J, Long Qi, Shen Li
University of Pennsylvania, Philadelphia, PA, USA.
Indiana University, Indianapolis, IN, USA.
AMIA Jt Summits Transl Sci Proc. 2025 Jun 10;2025:141-148. eCollection 2025.
Alzheimer's Disease (AD) is a neurodegenerative disorder marked by cognitive and functional decline. Biological sex has been linked to differences in lifetime AD risk, AD-related neuropathology, and the rate of cognitive decline, although the underlying biological mechanisms driving these disparities remain unclear. Epigenetic Age Acceleration-a metric derived from epigenetic aging clocks-has been associated with numerous aging-related conditions such as AD. Although there is promise in using Epigenetic age acceleration as a biomarker for several aging related diseases, the underlying mechanism that aging clocks are actually predicting is not well understood. In this study, we used data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to examine how sex influences the relationship between age acceleration and cognitive performance as well as brain volume. Our findings suggest that, although epigenetic age acceleration can predict changes in brain structure, these changes don't appear to be different across sexes. Future research should focus on validating these findings in an external cohort and exploring them longitudinally.
阿尔茨海默病(AD)是一种以认知和功能衰退为特征的神经退行性疾病。生物学性别与终生患AD风险、AD相关神经病理学以及认知衰退速度的差异有关,尽管导致这些差异的潜在生物学机制尚不清楚。表观遗传年龄加速——一种从表观遗传衰老时钟得出的指标——已与许多与衰老相关的疾病(如AD)相关联。尽管将表观遗传年龄加速用作几种与衰老相关疾病的生物标志物很有前景,但衰老时钟实际预测的潜在机制尚未得到很好的理解。在本研究中,我们使用了来自阿尔茨海默病神经影像学倡议(ADNI)的数据,以研究性别如何影响年龄加速与认知表现以及脑容量之间的关系。我们的研究结果表明,尽管表观遗传年龄加速可以预测脑结构的变化,但这些变化在不同性别之间似乎并无差异。未来的研究应集中在外部队列中验证这些发现并进行纵向探索。