针对表观遗传上较老的个体进行老年保护试验:使用DNA甲基化时钟。

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY Biogerontology Pub Date : 2024-06-01 Epub Date: 2023-11-16 DOI:10.1007/s10522-023-10077-4
Elena Sandalova, Andrea B Maier
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引用次数: 0

摘要

实足年龄是年龄相关疾病发生的最重要的危险因素。衰老的速度决定了这种风险的大小,可以用生物年龄来表达。用老年保护剂瞄准人类衰老的基本途径有可能降低生物年龄,从而延长健康期,即一个人在健康状态下度过的生命周期。应根据正在处理的老龄化机制和老年保护器对主要结果的预期影响来选择老年人保护干预措施的目标人群。衰老的生物标志物,如DNA甲基化年龄,可用于选择人群进行老年保护干预,并作为替代结果。在这里,使用DNA甲基化时钟来选择目标人群进行老年保护干预的探索。
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Targeting the epigenetically older individuals for geroprotective trials: the use of DNA methylation clocks.

Chronological age is the most important risk factor for the incidence of age-related diseases. The pace of ageing determines the magnitude of that risk and can be expressed as biological age. Targeting fundamental pathways of human aging with geroprotectors has the potential to lower the biological age and therewith prolong the healthspan, the period of life one spends in good health. Target populations for geroprotective interventions should be chosen based on the ageing mechanisms being addressed and the expected effect of the geroprotector on the primary outcome. Biomarkers of ageing, such as DNA methylation age, can be used to select populations for geroprotective interventions and as a surrogate outcome. Here, the use of DNA methylation clocks for selecting target populations for geroprotective intervention is explored.

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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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