健康衰老
标准化
精密医学
生物年龄
风险分析(工程)
医学
干预(咨询)
表观遗传学
后生
营养基因学
生物信息学
机制(生物学)
微生物群
计算机科学
计算生物学
转化研究
范式转换
个性化医疗
生物
公共卫生
肠道微生物群
老年学
疾病
梅德林
系统生物学
作者
So-Hyun Park,Chang Hwa Jung,Jiyun Ahn
标识
DOI:10.5483/bmbrep.2025-0216
摘要
Aging is a multifactorial and heterogeneous biological process, where chronological age alone does not accurately reflect an individual's functional or physiological state. The emerging discipline of precision geronutrition integrates the principles of geroscience with precision nutrition, aiming to delay the onset of age-related functional decline by modulating fundamental molecular mechanisms, such as nutrient-sensing pathways (mTOR, AMPK, and sirtuins), inflammaging, and oxidative stress. A major barrier to progress has been the absence of validated biomarkers that can quantify biological aging and assess intervention efficacy. Recent advances in biological aging clocks, in particular DNA methylation-based epigenetic clocks, provide powerful tools to objectively measure biological age, and evaluate the impact of nutritional interventions. This review discusses how personalized dietary strategies, guided by multi-omics data (genomic, metabolomic, and microbiome profiles), can decelerate aging trajectories. We propose that individualized daily nutrition, aligned with an individual's unique biological characteristics, represents a targeted and actionable approach to extend healthspan. The integration of dynamic aging clocks into nutritional intervention frameworks will be essential to transition from a diseaseoriented model to a preventive, healthspan-centered paradigm. Future challenges include large-scale clinical validation, standardization of aging biomarkers, cost reduction, and translation into public health and clinical applications. [BMB Reports 2026; 59(1): 51-59].
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