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表观遗传年龄介导生活必需 8 要素与心血管疾病和死亡率的关联。

Epigenetic Age Mediates the Association of Life's Essential 8 With Cardiovascular Disease and Mortality.

机构信息

Population Sciences Branch, Division of Intramural Research, National Heart, Lung, and Blood Institute National Institutes of Health Bethesda MD.

Framingham Heart Study Framingham MA.

出版信息

J Am Heart Assoc. 2024 Jun 4;13(11):e032743. doi: 10.1161/JAHA.123.032743. Epub 2024 May 29.

Abstract

BACKGROUND

Life's Essential 8 (LE8) is an enhanced metric for cardiovascular health. The interrelations among LE8, biomarkers of aging, and disease risks are unclear.

METHODS AND RESULTS

LE8 score was calculated for 5682 Framingham Heart Study participants. We implemented 4 DNA methylation-based epigenetic age biomarkers, with older epigenetic age hypothesized to represent faster biological aging, and examined whether these biomarkers mediated the associations between the LE8 score and cardiovascular disease (CVD), CVD-specific mortality, and all-cause mortality. We found that a 1 SD increase in the LE8 score was associated with a 35% (95% CI, 27-41; =1.8E-15) lower risk of incident CVD, a 36% (95% CI, 24-47; =7E-7) lower risk of CVD-specific mortality, and a 29% (95% CI, 22-35; =7E-15) lower risk of all-cause mortality. These associations were partly mediated by epigenetic age biomarkers, particularly the GrimAge and the DunedinPACE scores. The potential mediation effects by epigenetic age biomarkers tended to be more profound in participants with higher genetic risk for older epigenetic age, compared with those with lower genetic risk. For example, in participants with higher GrimAge polygenic scores (greater than median), the mean proportion of mediation was 39%, 39%, and 78% for the association of the LE8 score with incident CVD, CVD-specific mortality, and all-cause mortality, respectively. No significant mediation was observed in participants with lower GrimAge polygenic score.

CONCLUSIONS

DNA methylation-based epigenetic age scores mediate the associations between the LE8 score and incident CVD, CVD-specific mortality, and all-cause mortality, particularly in individuals with higher genetic predisposition for older epigenetic age.

摘要

背景

生命基础 8(LE8)是一种增强的心血管健康指标。LE8 与衰老生物标志物和疾病风险之间的相互关系尚不清楚。

方法和结果

为 5682 名弗雷明汉心脏研究参与者计算了 LE8 评分。我们实施了 4 种基于 DNA 甲基化的表观遗传年龄生物标志物,假设较老的表观遗传年龄代表更快的生物衰老,并研究了这些生物标志物是否介导了 LE8 评分与心血管疾病(CVD)、CVD 特异性死亡率和全因死亡率之间的关联。我们发现,LE8 评分增加 1 个标准差与 CVD 事件风险降低 35%(95%CI,27-41;=1.8E-15)、CVD 特异性死亡率降低 36%(95%CI,24-47;=7E-7)和全因死亡率降低 29%(95%CI,22-35;=7E-15)相关。这些关联部分通过表观遗传年龄生物标志物介导,特别是 GrimAge 和 DunedinPACE 评分。与遗传上具有较老表观遗传年龄较低风险的参与者相比,具有较高遗传上具有较老表观遗传年龄较高风险的参与者中,表观遗传年龄生物标志物的潜在中介作用更为明显。例如,在具有较高 GrimAge 多基因评分(大于中位数)的参与者中,LE8 评分与 CVD 事件、CVD 特异性死亡率和全因死亡率相关的平均中介比例分别为 39%、39%和 78%。在具有较低 GrimAge 多基因评分的参与者中,未观察到显著的中介作用。

结论

基于 DNA 甲基化的表观遗传年龄评分介导了 LE8 评分与 CVD 事件、CVD 特异性死亡率和全因死亡率之间的关联,尤其是在遗传上具有较老表观遗传年龄较高倾向的个体中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/410c/11255626/faeb2c62f5e7/JAH3-13-e032743-g002.jpg

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