Advanced Technology Center for Aging Research and Geriatric Mouse Clinic, IRCCS INRCA, 60121, Ancona, Italy.
Scientific Direction, IRCCS INRCA, 60124, Ancona, Italy.
Geroscience. 2023 Dec;45(6):3267-3305. doi: 10.1007/s11357-023-00960-w. Epub 2023 Oct 4.
Senescent cells may have a prominent role in driving inflammation and frailty. The impact of cellular senescence on frailty varies depending on the assessment tool used, as it is influenced by the criteria or items predominantly affected by senescent cells and the varying weights assigned to these items across different health domains. To address this challenge, we undertook a thorough review of all available studies involving gain- or loss-of-function experiments as well as interventions targeting senescent cells, focusing our attention on those studies that examined outcomes based on the individual frailty phenotype criteria or specific items used to calculate two humans (35 and 70 items) and one mouse (31 items) frailty indexes. Based on the calculation of a simple "evidence score," we found that the burden of senescent cells related to musculoskeletal and cerebral health has the strongest causal link to frailty. We deem that insight into these mechanisms may not only contribute to clarifying the role of cellular senescence in frailty but could additionally provide multiple therapeutic opportunities to help the future development of a desirable personalized therapy in these extremely heterogeneous patients.
衰老细胞可能在驱动炎症和虚弱方面起着重要作用。细胞衰老对虚弱的影响因所使用的评估工具而异,因为它受到衰老细胞主要影响的标准或项目以及不同健康领域对这些项目的权重分配的影响。为了应对这一挑战,我们对所有涉及获得或丧失功能实验以及针对衰老细胞的干预措施的研究进行了全面审查,重点关注那些根据个体虚弱表型标准或用于计算两个人类(35 项和 70 项)和一只老鼠(31 项)虚弱指数的特定项目来检查结果的研究。基于简单的“证据评分”的计算,我们发现与肌肉骨骼和大脑健康相关的衰老细胞负担与虚弱之间存在最强的因果关系。我们认为,深入了解这些机制不仅有助于阐明细胞衰老在虚弱中的作用,而且还可能为治疗提供多种机会,以帮助未来在这些极其异质的患者中开发理想的个体化治疗方法。