Milicic Lidija, Porter Tenielle, Vacher Michael, Laws Simon M
Centre for Precision Health, Edith Cowan University, Joondalup, Western Australia, Australia.
Collaborative Genomics and Translation Group, Edith Cowan University, Joondalup, Western Australia, Australia.
J Alzheimers Dis Rep. 2023 May 31;7(1):475-503. doi: 10.3233/ADR-220109. eCollection 2023.
Epigenetic mechanisms such as DNA methylation have been implicated in a number of diseases including cancer, heart disease, autoimmune disorders, and neurodegenerative diseases. While it is recognized that DNA methylation is tissue-specific, a limitation for many studies is the ability to sample the tissue of interest, which is why there is a need for a proxy tissue such as blood, that is reflective of the methylation state of the target tissue. In the last decade, DNA methylation has been utilized in the design of epigenetic clocks, which aim to predict an individual's biological age based on an algorithmically defined set of CpGs. A number of studies have found associations between disease and/or disease risk with increased biological age, adding weight to the theory of increased biological age being linked with disease processes. Hence, this review takes a closer look at the utility of DNA methylation as a biomarker in aging and disease, with a particular focus on Alzheimer's disease.
DNA甲基化等表观遗传机制与包括癌症、心脏病、自身免疫性疾病和神经退行性疾病在内的多种疾病有关。虽然人们认识到DNA甲基化具有组织特异性,但许多研究的一个局限在于获取感兴趣组织样本的能力,这就是为什么需要像血液这样能够反映目标组织甲基化状态的替代组织。在过去十年中,DNA甲基化已被用于表观遗传时钟的设计,表观遗传时钟旨在根据一组通过算法定义的CpG来预测个体的生物学年龄。许多研究发现疾病和/或疾病风险与生物学年龄增加之间存在关联,这进一步支持了生物学年龄增加与疾病进程相关的理论。因此,本综述将更深入地探讨DNA甲基化作为衰老和疾病生物标志物的效用,尤其关注阿尔茨海默病。