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美国成年人的表观遗传年龄加速与死亡风险预测

Epigenetic age acceleration and mortality risk prediction in U.S. adults.

作者信息

Mendy Angelico, Mersha Tesfaye B

机构信息

Division of Epidemiology, Department of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH.

Division of Asthma Research, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH.

出版信息

medRxiv. 2024 Aug 29:2024.08.21.24312373. doi: 10.1101/2024.08.21.24312373.

Abstract

BACKGROUND

Epigenetic clocks have emerged as novel measures of biological age and potential predictors of mortality. We aimed to test whether epigenetic age acceleration (EAA) estimated using different epigenetic clocks predict long-term overall, cardiovascular or cancer mortality.

METHODS

We analyzed data from 2,105 participants to the 1999-2002 National Health and Nutrition Examination Survey aged ≥50 years old who were followed for mortality through 2019. EAAs was calculated from the residuals of Horvath, Hannum, SkinBlood, Pheno, Zhang, Lin, Weidner, Vidal-Bralo and Grim epigenetic clocks regressed on chronological age. Using cox proportional hazards regression, we estimated the hazard ratio (HR) and 95% confidence interval (CI) for the association of EAA (per 5-year) and the DunedinPoAm pace of aging (per 10% increase) with overall, cardiovascular and cancer mortality, adjusting for covariates and white blood cell composition.

RESULTS

During a median follow-up of 17.5 years, 998 deaths occurred, including 272 from cardiovascular disease and 209 from cancer. Overall mortality was most significantly predicted by Grim EAA ( < 0.0001; HR: 1.50, 95% CI: 1.32-1.71) followed by Hannum ( = 0.001; HR: 1.16, 95% CI: 1.07-1.27), Pheno ( = 0.001; HR: 1.13, 95% CI: 1.05-1.21), Horvath ( = 0.007; HR: 1.13, 95% CI: 1.04-1.22) and Vidal-Bralo ( = 0.008; HR: 1.13, 95% CI: 1.03-1.23) EAAs. Grim EAA predicted cardiovascular mortality ( < 0.0001; HR: 1.55, 95% CI: 1.29-1.86), whereas Hannum ( = 0.006; HR: 1.24, 95% CI: 1.07-1.44), Horvath ( = 0.02; HR: 1.18, 95% CI: 1.02-1.35) and Grim ( = 0.049; HR: 1.37, 95% CI: 1.00-1.87) EAAs predicted cancer mortality. DunedinPoAm pace of aging was associated with overall ( = 0.003; HR: 1.23, 95% CI: 1.08-1.38) and cardiovascular ( = 0.04; HR: 1.25, 95% CI: 1.01-1.55) mortality.

CONCLUSIONS

In a U.S. representative sample, Horvath, Hannum, Pheno, Vidal-Bralo and Grim EAA all predicted overall mortality but only Grim EAA predicted cardiovascular mortality and Horvath, Hannum or Grim EAA predicted cancer mortality. Pace of aging predicted overall and cardiovascular mortality.

摘要

背景

表观遗传时钟已成为衡量生物年龄的新指标和死亡率的潜在预测因子。我们旨在测试使用不同表观遗传时钟估计的表观遗传年龄加速(EAA)是否能预测长期总体、心血管或癌症死亡率。

方法

我们分析了来自1999 - 2002年国家健康与营养检查调查中2105名年龄≥50岁参与者的数据,这些参与者随访至2019年以获取死亡率信息。EAA是根据霍瓦斯(Horvath)、汉纳姆(Hannum)、皮肤血液(SkinBlood)、表型(Pheno)、张(Zhang)、林(Lin)、魏德纳(Weidner)、维达尔 - 布拉洛(Vidal - Bralo)和格里姆(Grim)表观遗传时钟与实足年龄回归后的残差计算得出。使用Cox比例风险回归,我们估计了EAA(每5年)和达尼丁多领域衰老加速量表(DunedinPoAm)衰老速度(每增加10%)与总体、心血管和癌症死亡率之间关联的风险比(HR)和95%置信区间(CI),并对协变量和白细胞组成进行了调整。

结果

在中位随访17.5年期间,发生了998例死亡,其中272例死于心血管疾病,209例死于癌症。总体死亡率最显著地由格里姆EAA预测(<0.0⺁01;HR:1.50,95%CI:1.32 - 1.71),其次是汉纳姆(=0.001;HR:1.16,95%CI:1.0⺁ - 1.27)、表型(=0.001;HR:1.13,95%CI:1.05 - 1.21)、霍瓦斯(=0.007;HR:1.13,95%CI:1.04 - 1.22)和维达尔 - 布拉洛(=0.008;HR:1.13,95%CI:1.03 - 1.23)EAA。格里姆EAA预测心血管死亡率(<0.0⺁01;HR:1.55,95%CI:1.29 - 1.86),而汉纳姆(=0.006;HR:1.24,95%CI:1.0⺁ - 1.44)、霍瓦斯(=0.02;HR:1.18,95%CI:1.02 - 1.35)和格里姆(=0.049;HR:1.37,95%CI:1.00 - 1.87)EAA预测癌症死亡率。达尼丁多领域衰老加速量表的衰老速度与总体(=0.003;HR:1.23,95%CI:1.08 - 1.38)和心血管(=0.04;HR:1.25,95%CI:1.01 - 1.55)死亡率相关。

结论

在美国代表性样本中,霍瓦斯、汉纳姆、表型、维达尔 - 布拉洛和格里姆EAA均能预测总体死亡率,但只有格里姆EAA能预测心血管死亡率;霍瓦斯、汉纳姆或格里姆EAA能预测癌症死亡率。衰老速度能预测总体和心血管死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b12/11370508/c1b20d92640c/nihpp-2024.08.21.24312373v2-f0001.jpg

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