表观遗传学
生物
DNA甲基化
生物年龄
疾病
健康衰老
后生
衰老
生物信息学
计算生物学
进化生物学
老年学
遗传学
医学
病理
基因表达
基因
作者
Joshua J. Levy,Alos Diallo,Marietta K. Saldias Montivero,Sameer Gabbita,Lucas A. Salas,Brock C. Christensen
出处
期刊:Epigenomics
[Future Medicine]
日期:2024-11-25
卷期号:: 1-9
标识
DOI:10.1080/17501911.2024.2432854
摘要
Over the past century, human lifespan has increased remarkably, yet the inevitability of aging persists. The disparity between biological age, which reflects pathological deterioration and disease, and chronological age, indicative of normal aging, has driven prior research focused on identifying mechanisms that could inform interventions to reverse excessive age-related deterioration and reduce morbidity and mortality. DNA methylation has emerged as an important predictor of age, leading to the development of epigenetic clocks that quantify the extent of pathological deterioration beyond what is typically expected for a given age. Machine learning technologies offer promising avenues to enhance our understanding of the biological mechanisms governing aging by further elucidating the gap between biological and chronological ages. This perspective article examines current algorithmic approaches to epigenetic clocks, explores the use of machine learning for age estimation from DNA methylation, and discusses how refining the interpretation of ML methods and tailoring their inferences for specific patient populations and cell types can amplify the utility of these technologies in age prediction. By harnessing insights from machine learning, we are well-positioned to effectively adapt, customize and personalize interventions aimed at aging.
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