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在人类中,由氧化应激引起的 RNA 与 DNA 损伤对死亡率的特异性预测。

Specific prediction of mortality by oxidative stress-induced damage to RNA vs. DNA in humans.

机构信息

Psychiatric Center Copenhagen, Mental Health Services, Copenhagen, Denmark.

Institute of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Aging Cell. 2023 Jun;22(6):e13839. doi: 10.1111/acel.13839. Epub 2023 May 15.

Abstract

Modifications of nucleic acids (DNA and RNA) from oxidative stress is a potential driver of aging per se and of mortality in age-associated medical disorders such as type 2 diabetes (T2D). In a human cohort, we found a strong prediction of all-cause mortality by a marker of systemic oxidation of RNA in patients with T2D (n = 2672) and in nondiabetic control subjects (n = 4079). The finding persisted after the adjustment of established modifiers of oxidative stress (including BMI, smoking, and glycated hemoglobin). In contrast, systemic levels of DNA damage from oxidation, which traditionally has been causally linked to both T2D and aging, failed to predict mortality. Strikingly, these findings were subsequently replicated in an independent general population study (n = 3649). The data demonstrate a specific importance of RNA damage from oxidation in T2D and general aging.

摘要

氧化应激导致的核酸(DNA 和 RNA)修饰本身是衰老的潜在驱动因素,也是与年龄相关的医学疾病(如 2 型糖尿病(T2D))中死亡率的潜在驱动因素。在一项人类队列研究中,我们发现 T2D 患者(n=2672)和非糖尿病对照受试者(n=4079)的 RNA 系统氧化标志物强烈预测了全因死亡率。在调整了氧化应激的既定修饰物(包括 BMI、吸烟和糖化血红蛋白)后,这一发现仍然存在。相比之下,传统上与 T2D 和衰老均有关联的氧化导致的 DNA 损伤的系统水平未能预测死亡率。令人惊讶的是,这些发现随后在一项独立的一般人群研究中得到了复制(n=3649)。这些数据表明氧化导致的 RNA 损伤在 T2D 和一般衰老中具有特殊的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/041e/10265158/0fb51f7f030b/ACEL-22-e13839-g004.jpg

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