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2
Examination of the Dimensions of Biological Age.生物年龄维度的检验
Front Genet. 2019 Mar 26;10:263. doi: 10.3389/fgene.2019.00263. eCollection 2019.
3
An epigenetic biomarker of aging for lifespan and healthspan.一种用于寿命和健康寿命的衰老表观遗传生物标志物。
Aging (Albany NY). 2018 Apr 18;10(4):573-591. doi: 10.18632/aging.101414.
4
DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins.丹麦中年及老年双胞胎的DNA甲基化与全因死亡率
Genes (Basel). 2018 Feb 8;9(2):78. doi: 10.3390/genes9020078.
5
Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins.中年同卵双胞胎认知功能的全表观基因组关联研究
Front Aging Neurosci. 2017 Dec 12;9:413. doi: 10.3389/fnagi.2017.00413. eCollection 2017.
6
Unifying aging and frailty through complex dynamical networks.通过复杂动态网络统一衰老和脆弱。
Exp Gerontol. 2018 Jul 1;107:126-129. doi: 10.1016/j.exger.2017.08.027. Epub 2017 Aug 25.
7
Methylation of the ribosomal RNA gene promoter is associated with aging and age-related decline.核糖体 RNA 基因启动子的甲基化与衰老和与年龄相关的衰退有关。
Aging Cell. 2017 Oct;16(5):966-975. doi: 10.1111/acel.12603. Epub 2017 Jun 17.
8
Biological Aging and the Human Gut Microbiota.生物衰老与人类肠道微生物群
J Gerontol A Biol Sci Med Sci. 2017 Oct 12;72(11):1474-1482. doi: 10.1093/gerona/glx042.
9
The frailty index outperforms DNA methylation age and its derivatives as an indicator of biological age.衰弱指数在作为生物年龄指标方面优于 DNA 甲基化年龄及其衍生指标。
Geroscience. 2017 Feb;39(1):83-92. doi: 10.1007/s11357-017-9960-3. Epub 2017 Jan 14.
10
Heterogeneity of Human Aging and Its Assessment.人类衰老的异质性及其评估
J Gerontol A Biol Sci Med Sci. 2017 Jul 1;72(7):877-884. doi: 10.1093/gerona/glw089.

特征选择算法可提高衰弱指数作为生物年龄衡量指标的准确性。

Feature Selection Algorithms Enhance the Accuracy of Frailty Indexes as Measures of Biological Age.

机构信息

Tulane Center for Aging and Department of Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana, USA.

Department of Medicine, Louisiana State University Health Sciences Center, New Orleans, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2021 Jul 13;76(8):1347-1355. doi: 10.1093/gerona/glab018.

DOI:10.1093/gerona/glab018
PMID:33471059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8277082/
Abstract

Biological age captures some of the variance in life expectancy for which chronological age is not accountable, and it quantifies the heterogeneity in the presentation of the aging phenotype in various individuals. Among the many quantitative measures of biological age, the mathematically uncomplicated frailty/deficit index is simply the proportion of the total health deficits in various health items surveyed in different individuals. We used 3 different statistical methods that are popular in machine learning to select 17-28 health items that together are highly predictive of survival/mortality, from independent study cohorts. From the selected sets, we calculated frailty indexes and Klemera-Doubal's biological age estimates, and then compared their mortality prediction performance using Cox proportional hazards regression models. Our results indicate that the frailty index outperforms age and Klemera-Doubal's biological age estimates, especially among the oldest old who are most prone to biological aging-caused mortality. We also showed that a DNA methylation index, which was generated by applying the frailty/deficit index calculation method to 38 CpG sites that were selected using the same machine learning algorithms, can predict mortality even better than the best performing frailty index constructed from health, function, and blood chemistry.

摘要

生物年龄可以捕捉到一些与预期寿命相关的、无法用年龄解释的差异,它量化了不同个体中衰老表型的异质性。在许多生物年龄的定量衡量标准中,数学上简单的脆弱/缺陷指数只是在不同个体中调查的各种健康项目的总健康缺陷的比例。我们使用了机器学习中流行的 3 种不同的统计方法,从独立的研究队列中选择了 17-28 项健康项目,这些项目共同高度预测了生存/死亡率。从选定的集合中,我们计算了脆弱性指数和 Klemera-Doubal 的生物年龄估计值,然后使用 Cox 比例风险回归模型比较了它们的死亡率预测性能。我们的结果表明,脆弱性指数优于年龄和 Klemera-Doubal 的生物年龄估计值,尤其是在最容易受到生物老化导致死亡的最年长的老年人中。我们还表明,通过应用脆弱/缺陷指数计算方法生成的 DNA 甲基化指数,使用相同的机器学习算法选择的 38 个 CpG 位点,可以更好地预测死亡率,甚至比从健康、功能和血液化学构建的表现最好的脆弱性指数更好。