与生活方式、疾病和死亡率相关的器官特异性蛋白质组衰老模式

IF 7.1 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-10-08 DOI:10.1111/acel.70251
Qi Wang, Jingting Huang, Qida He, Mengtong Sun, Michael P Snyder, Linyan Li
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引用次数: 0

摘要

衰老在不同器官中以异质方式发生,导致慢性疾病和死亡的风险不同。生物年龄更全面地反映了衰老过程,是疾病风险和寿命的一个更强的预测指标。血浆蛋白质组学的最新进展使器官特异性衰老时钟的发展成为可能,揭示了不同的衰老轨迹及其临床意义。我们对11个器官使用了基于蛋白质的老化估计器,并使用弹性网正则化将其应用于血浆数据。通过全现象关联研究(PheWAS)对86种生活方式和环境因素、657种疾病以及全因死亡率进行了综合分析。我们的研究结果表明,器官衰老受生活方式因素和基线健康状况的影响,突出了其动态和可改变的性质。此外,器官老化加速与疾病发病率升高和全因死亡风险增加有关,特别是在生命早期发生时。我们的大规模生活方式图谱和PheWAS为器官衰老的可改变驱动因素提供了可操作的见解,推进了疾病预防和长寿的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Organ-Specific Proteomic Aging in Relation to Lifestyle, Diseases, and Mortality.

Aging occurs in a heterogeneous manner across different organs, leading to varying risks of chronic diseases and mortality. Biological age offers a more comprehensive reflection of the aging process and is a stronger predictor of disease risk and lifespan. Recent advances in plasma proteomics have enabled the development of organ-specific aging clocks, revealing the distinct aging trajectories and their clinical implications. We used protein-based aging estimators for 11 organs, applying them to plasma data using elastic net regularization. A comprehensive analysis of associations was conducted with 86 lifestyle and environmental factors, 657 diseases through phenome-wide association studies (PheWAS), and all-cause mortality. Our findings revealed that organ aging is influenced by lifestyle factors and baseline health conditions, highlighting its dynamic and modifiable nature. Additionally, accelerated organ aging is associated with a higher incidence of disease and an increased risk of all-cause mortality, particularly when it occurs earlier in life. Our large-scale lifestyle atlas and PheWAS offer actionable insights into the modifiable drivers of organ aging, advancing strategies for disease prevention and longevity.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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