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p16Ink4a作为自然衰老过程中生理衰退早期预测指标的作用

The Role of p16Ink4a as an Early Predictor of Physiological Decline during Natural Aging.

作者信息

Tang Lingzi, Hladyshau Siarhei, Ross Allison, Nyrop Kirsten A, Entwistle Amy, Muss Hyman B, Mitin Natalia, Tsygankov Denis

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University SOM, Atlanta, GA 30332.

School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332.

出版信息

medRxiv. 2024 Nov 22:2024.11.21.24317752. doi: 10.1101/2024.11.21.24317752.

DOI:10.1101/2024.11.21.24317752
PMID:39606419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11601678/
Abstract

Cellular senescence is a prominent accomplice of aging. The expression of gene p16ink4a has been established as a biomarker of cellular senescence in humans and animal models. However, it has not been extensively studied in clinical settings in the context of natural aging and the development of age-related diseases. Here, we report the results of a natural aging study that provided an assessment of cellular senescence and a battery of measures of clinical status, quality of life (QOL), and physical performance in 250 community-dwelling participants across age continuum. This report focused on analyzing predictive relationships between cellular senescence and different clinical assessments. Our results suggest that clinical labs and QOL assessments produce distinct groupings of participants, yet both have strong predictive associations with p16ink4a. Furthermore, the highest accuracy of p16ink4a prediction requires subsets of measurements representing diverse aspects of each assessment, pointing towards a system-level role of p16ink4a. Our analysis also led to an assessment-based composite indexes that strongly correlate with p16ink4a expression. Our study underscores p16ink4a's association with both earlier signs of physiological decline (based on clinical labs) and the later onset of health issues limiting the quality of life.

摘要

细胞衰老显然是衰老的一个因素。在人类和动物模型中,基因p16ink4a的表达已被确立为细胞衰老的生物标志物。然而,在自然衰老和年龄相关疾病发展的临床背景下,尚未对其进行广泛研究。在此,我们报告一项自然衰老研究的结果,该研究对250名不同年龄段的社区居民参与者的细胞衰老情况以及一系列临床状况、生活质量(QOL)和身体机能指标进行了评估。本报告重点分析细胞衰老与不同临床评估之间的预测关系。我们的结果表明,临床实验室检查和生活质量评估产生了不同的参与者分组,但两者都与p16ink4a有很强的预测关联。此外,p16ink4a预测的最高准确性需要代表每项评估不同方面的测量子集,这表明p16ink4a具有系统层面的作用。我们的分析还得出了与p16ink4a表达密切相关的基于评估的综合指数。我们的研究强调了p16ink4a与生理衰退的早期迹象(基于临床实验室检查)以及限制生活质量的健康问题的后期出现均有关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/b5ea6575c20e/nihpp-2024.11.21.24317752v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/548a823978c5/nihpp-2024.11.21.24317752v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/1945ec073df2/nihpp-2024.11.21.24317752v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/14127ba9cc8c/nihpp-2024.11.21.24317752v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/6c7922f0643f/nihpp-2024.11.21.24317752v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/aa9d72927220/nihpp-2024.11.21.24317752v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/1369d95858bf/nihpp-2024.11.21.24317752v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/15976c74f873/nihpp-2024.11.21.24317752v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/b5ea6575c20e/nihpp-2024.11.21.24317752v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/548a823978c5/nihpp-2024.11.21.24317752v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/1945ec073df2/nihpp-2024.11.21.24317752v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/14127ba9cc8c/nihpp-2024.11.21.24317752v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/6c7922f0643f/nihpp-2024.11.21.24317752v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/aa9d72927220/nihpp-2024.11.21.24317752v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/1369d95858bf/nihpp-2024.11.21.24317752v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/15976c74f873/nihpp-2024.11.21.24317752v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef8/11601678/b5ea6575c20e/nihpp-2024.11.21.24317752v1-f0008.jpg

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本文引用的文献

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