• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

认知不确定性挑战了衰老时钟预测年轻化效果的可靠性。

Epistemic uncertainty challenges aging clock reliability in predicting rejuvenation effects.

机构信息

Skolkovo Institute of Science and Technology, Moscow, Russia.

Artificial Intelligence Research Institute, Moscow, Russia.

出版信息

Aging Cell. 2024 Nov;23(11):e14283. doi: 10.1111/acel.14283. Epub 2024 Jul 28.

DOI:10.1111/acel.14283
PMID:39072888
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11561706/
Abstract

Epigenetic aging clocks have been widely used to validate rejuvenation effects during cellular reprogramming. However, these predictions are unverifiable because the true biological age of reprogrammed cells remains unknown. We present an analytical framework to consider rejuvenation predictions from the uncertainty perspective. Our analysis reveals that the DNA methylation profiles across reprogramming are poorly represented in the aging data used to train clock models, thus introducing high epistemic uncertainty in age estimations. Moreover, predictions of different published clocks are inconsistent, with some even suggesting zero or negative rejuvenation. While not questioning the possibility of age reversal, we show that the high clock uncertainty challenges the reliability of rejuvenation effects observed during in vitro reprogramming before pluripotency and throughout embryogenesis. Conversely, our method reveals a significant age increase after in vivo reprogramming. We recommend including uncertainty estimation in future aging clock models to avoid the risk of misinterpreting the results of biological age prediction.

摘要

表观遗传衰老时钟已被广泛用于验证细胞重编程过程中的年轻化效果。然而,这些预测是无法验证的,因为重编程细胞的真实生物学年龄仍然未知。我们提出了一个分析框架,从不确定性的角度来考虑年轻化预测。我们的分析表明,在用于训练时钟模型的衰老数据中,重编程过程中的 DNA 甲基化图谱代表性很差,因此在年龄估计中引入了高度的认知不确定性。此外,不同已发表时钟的预测结果不一致,有些甚至表明零或负年轻化。虽然我们不质疑年龄逆转的可能性,但我们表明,高时钟不确定性挑战了体外重编程过程中在多能性之前和整个胚胎发生过程中观察到的年轻化效果的可靠性。相反,我们的方法显示体内重编程后年龄显著增加。我们建议在未来的衰老时钟模型中纳入不确定性估计,以避免错误解释生物年龄预测结果的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/6f30d79afef5/ACEL-23-e14283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/200e4cc6b5b7/ACEL-23-e14283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/99a64bc0f4fc/ACEL-23-e14283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/b46ce3b04985/ACEL-23-e14283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/68a1327520f8/ACEL-23-e14283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/6f30d79afef5/ACEL-23-e14283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/200e4cc6b5b7/ACEL-23-e14283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/99a64bc0f4fc/ACEL-23-e14283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/b46ce3b04985/ACEL-23-e14283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/68a1327520f8/ACEL-23-e14283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d9/11561706/6f30d79afef5/ACEL-23-e14283-g005.jpg

相似文献

1
Epistemic uncertainty challenges aging clock reliability in predicting rejuvenation effects.认知不确定性挑战了衰老时钟预测年轻化效果的可靠性。
Aging Cell. 2024 Nov;23(11):e14283. doi: 10.1111/acel.14283. Epub 2024 Jul 28.
2
Cellular reprogramming and epigenetic rejuvenation.细胞重编程和表观遗传再年轻化。
Clin Epigenetics. 2021 Sep 6;13(1):170. doi: 10.1186/s13148-021-01158-7.
3
Unveiling epigenetic regulation in cancer, aging, and rejuvenation with in vivo reprogramming technology.利用体内重编程技术揭示癌症、衰老和 rejuvenation 中的表观遗传调控。
Cancer Sci. 2018 Sep;109(9):2641-2650. doi: 10.1111/cas.13731. Epub 2018 Aug 15.
4
Mechanisms of cellular rejuvenation.细胞再生活跃的机制。
FEBS Lett. 2019 Dec;593(23):3381-3392. doi: 10.1002/1873-3468.13483. Epub 2019 Jun 24.
5
Epigenetic Age Reversal by Cell-Extrinsic and Cell-Intrinsic Means.通过细胞外源性和细胞内源性方式实现表观遗传年龄逆转。
Rejuvenation Res. 2019 Oct;22(5):439-446. doi: 10.1089/rej.2019.2271.
6
Epigenetic rejuvenation by partial reprogramming.部分重编程的表观遗传年轻化。
Bioessays. 2023 Apr;45(4):e2200208. doi: 10.1002/bies.202200208. Epub 2023 Mar 4.
7
Epigenetic reprogramming as a key to reverse ageing and increase longevity.表观遗传重编程作为逆转衰老和延长寿命的关键。
Ageing Res Rev. 2024 Mar;95:102204. doi: 10.1016/j.arr.2024.102204. Epub 2024 Jan 23.
8
Aging and rejuvenation - a modular epigenome model.衰老与 rejuvenation-模块化表观基因组模型。
Aging (Albany NY). 2021 Feb 24;13(4):4734-4746. doi: 10.18632/aging.202712.
9
Meiosis as a mechanism for epigenetic reprogramming and cellular rejuvenation.减数分裂作为表观遗传重编程和细胞 rejuvenation 的一种机制。
Development. 2024 Oct 15;151(20). doi: 10.1242/dev.203046. Epub 2024 Oct 14.
10
Transient non-integrative expression of nuclear reprogramming factors promotes multifaceted amelioration of aging in human cells.瞬时非整合性表达核重编程因子促进人细胞衰老的多方面改善。
Nat Commun. 2020 Mar 24;11(1):1545. doi: 10.1038/s41467-020-15174-3.

引用本文的文献

1
First-generation versus next-generation epigenetic aging clocks: Differences in performance and utility.第一代与新一代表观遗传衰老时钟:性能与效用的差异
Biogerontology. 2025 Jun 18;26(4):121. doi: 10.1007/s10522-025-10265-4.
2
A Novel Framework for the Design of Minimized Epigenetic Clocks Using the Analysis of DNA Methylation Heterogeneity.一种基于DNA甲基化异质性分析设计最小化表观遗传时钟的新框架。
Int J Mol Sci. 2025 May 23;26(11):5051. doi: 10.3390/ijms26115051.
3
The COVID-19 legacy: consequences for the human DNA methylome and therapeutic perspectives.

本文引用的文献

1
Aging clocks based on accumulating stochastic variation.基于累积随机变化的衰老时钟。
Nat Aging. 2024 Jun;4(6):871-885. doi: 10.1038/s43587-024-00619-x. Epub 2024 May 9.
2
Nature of epigenetic aging from a single-cell perspective.从单细胞角度看表观遗传衰老的本质。
Nat Aging. 2024 Jun;4(6):854-870. doi: 10.1038/s43587-024-00616-0. Epub 2024 May 9.
3
Quantifying the stochastic component of epigenetic aging.量化表观遗传衰老的随机成分。
新冠疫情的遗留影响:对人类DNA甲基化组的后果及治疗前景。
Geroscience. 2025 Feb;47(1):483-501. doi: 10.1007/s11357-024-01406-7. Epub 2024 Nov 5.
Nat Aging. 2024 Jun;4(6):886-901. doi: 10.1038/s43587-024-00600-8. Epub 2024 May 9.
4
Clarifying the biological and statistical assumptions of cross-sectional biological age predictors: an elaborate illustration using synthetic and real data.厘清横向生物学年龄预测指标的生物学和统计学假设:使用合成与真实数据的详细说明。
BMC Med Res Methodol. 2024 Mar 8;24(1):58. doi: 10.1186/s12874-024-02181-x.
5
In vivo reprogramming leads to premature death linked to hepatic and intestinal failure.体内重编程导致与肝和肠衰竭相关的过早死亡。
Nat Aging. 2023 Dec;3(12):1509-1520. doi: 10.1038/s43587-023-00528-5. Epub 2023 Nov 27.
6
Intersection clock reveals a rejuvenation event during human embryogenesis.交集时钟揭示了人类胚胎发生过程中的一个年轻化事件。
Aging Cell. 2023 Oct;22(10):e13922. doi: 10.1111/acel.13922. Epub 2023 Oct 2.
7
Accurate age prediction from blood using a small set of DNA methylation sites and a cohort-based machine learning algorithm.使用一小部分 DNA 甲基化位点和基于队列的机器学习算法从血液中准确预测年龄。
Cell Rep Methods. 2023 Sep 25;3(9):100567. doi: 10.1016/j.crmeth.2023.100567. Epub 2023 Aug 28.
8
Fail-tests of DNA methylation clocks, and development of a noise barometer for measuring epigenetic pressure of aging and disease.DNA 甲基化钟的失效测试,以及开发一种噪声晴雨表来测量衰老和疾病的表观遗传压力。
Aging (Albany NY). 2023 Sep 12;15(17):8552-8575. doi: 10.18632/aging.205046.
9
Biomarkers of aging for the identification and evaluation of longevity interventions.衰老生物标志物用于鉴定和评估长寿干预措施。
Cell. 2023 Aug 31;186(18):3758-3775. doi: 10.1016/j.cell.2023.08.003.
10
Scientists hone tools to measure aging and rejuvenation interventions.科学家们完善用于测量衰老和年轻化干预措施的工具。
Nat Biotechnol. 2023 Oct;41(10):1359-1361. doi: 10.1038/d41587-023-00008-6.