年龄-疾病相互作用加速弹性蛋白降解:老年相关疾病的共同特征。

IF 4.1 Q2 GERIATRICS & GERONTOLOGY npj aging Pub Date : 2024-02-27 DOI:10.1038/s41514-024-00143-7
Naomi Shek, Anna-Maria Choy, Chim C Lang, Bruce E Miller, Ruth Tal-Singer, Charlotte E Bolton, Neil C Thomson, James D Chalmers, Matt J Bown, David E Newby, Faisel Khan, Jeffrey T J Huang
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引用次数: 0

摘要

衰老是许多疾病的主要驱动力,但人们对计时年龄、衰老过程和老年相关疾病之间的关系还不完全清楚。超长寿命弹性蛋白的碎裂和损失是衰老和多种老年相关疾病的主要特征,会导致死亡率上升。通过比较健康志愿者的年龄与弹性蛋白周转之间的关系,我们发现年龄-疾病相互作用导致的弹性蛋白加速周转是老年相关疾病的共同特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Accelerated elastin degradation by age-disease interaction: a common feature in age-related diseases.

Aging is a major driving force for many diseases but the relationship between chronological age, the aging process and age-related diseases is not fully understood. Fragmentation and loss of ultra-long-lived elastin are key features in aging and several age-related diseases leading to increased mortality. By comparing the relationship between age and elastin turnover with healthy volunteers, we show that accelerated elastin turnover by age-disease interaction is a common feature of age-related diseases.

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