dna甲基化年龄加速对美国心血管-肾-代谢综合征成人长期死亡率的影响

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of the American Heart Association Pub Date : 2025-04-01 Epub Date: 2025-03-21 DOI:10.1161/JAHA.124.039751
Shuang Wu, Jun Zhu, Siqi Lyu, Juan Wang, Xinghui Shao, Han Zhang, Ziyi Zhong, Hongyu Liu, Lihui Zheng, Yang Chen
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引用次数: 0

摘要

背景:在CKM综合征人群中,DNA甲基化年龄加速(DNAmAA)与心血管-肾-代谢(CKM)综合征分期和长期死亡率之间的关系尚不清楚。方法和结果:该队列研究纳入了1889名来自1999-2002年全国健康与营养调查的参与者,他们具有CKM分期和DNA甲基化年龄数据。DNAmAA作为DNA甲基化年龄对实足年龄回归的残差计算。主要结局为全因死亡率,心血管和非心血管死亡率为次要结局。比例优势模型评估了DNAmAAs与CKM分期之间的关系,Cox比例风险回归模型估计了DNAmAAs与死亡率之间的关系。DNAmAAs与晚期CKM之间存在显著相关性,尤其是GrimAA(比值比[OR], 1.547 [95% CI, 1.316-1.819])。在平均14年的随访中,有1015人死亡。GrimAA每增加5个单位,全因死亡率增加50% (95% CI, 1.39-1.63),心血管死亡率增加77% (95% CI, 1.46-2.15),非心血管死亡率增加42% (95% CI, 1.27-1.59)。以最低GrimAA指数为参照,最高GrimAA指数显示全因死亡率的风险比为1.95 (95% CI, 1.56-2.45),心血管死亡率的风险比为3.06 (95% CI, 2.13-4.40),非心血管死亡率的风险比为1.65 (95% CI, 1.20-2.29)。中介分析表明,GrimAA在各种暴露(包括体力活动、健康饮食指数-2015评分、血红蛋白A1c等)与死亡率之间起中介作用。结论:GrimAA可作为一种有价值的生物标志物,用于评估CKM分期和CKM综合征患者的死亡风险,从而为个性化的治疗策略提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of DNA-Methylation Age Acceleration on Long-Term Mortality Among US Adults With Cardiovascular-Kidney-Metabolic Syndrome.

Background: The association between DNA methylation age acceleration (DNAmAA) and cardiovascular-kidney-metabolic (CKM) syndrome stages and long-term mortality in the population with CKM syndrome remains unclear.

Methods and results: This cohort study included 1889 participants from the National Health and Nutrition Examination Survey (1999-2002) with CKM stages and DNA methylation age data. DNAmAA was calculated as residuals from the regression of DNA methylation age on chronological age. The primary outcome was all-cause mortality, with cardiovascular and noncardiovascular mortality as secondary outcomes. Proportional odds models assessed the associations between DNAmAAs and CKM stages, and Cox proportional hazards regression models estimated the associations between DNAmAAs and mortality. Significant associations were found between DNAmAAs and advanced CKM stages, particularly for GrimAge2Mort acceleration (GrimAA) (odds ratio [OR], 1.547 [95% CI, 1.316-1.819]). Over an average follow-up of 14 years, 1015 deaths occurred. Each 5-unit increase in GrimAA was associated with a 50% increase in all-cause mortality (95% CI, 1.39-1.63), a 77% increase in cardiovascular mortality (95% CI, 1.46-2.15), and a 42% increase in noncardiovascular mortality (95% CI, 1.27-1.59). With the lowest GrimAA tertile as a reference, the highest GrimAA tertile showed hazard ratios of 1.95 (95% CI, 1.56-2.45) for all-cause mortality, 3.06 (95% CI, 2.13-4.40) for cardiovascular mortality, and 1.65 (95% CI, 1.20-2.29) for noncardiovascular mortality. Mediation analysis indicated that GrimAA mediates the association between various exposures (including physical activity, Healthy Eating Index-2015 score, hemoglobin A1c, etc.) and mortality.

Conclusions: GrimAA may serve as a valuable biomarker for assessing CKM stages and mortality risk in individuals with CKM syndrome, thereby informing personalized management strategies.

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来源期刊
Journal of the American Heart Association
Journal of the American Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
9.40
自引率
1.90%
发文量
1749
审稿时长
12 weeks
期刊介绍: As an Open Access journal, JAHA - Journal of the American Heart Association is rapidly and freely available, accelerating the translation of strong science into effective practice. JAHA is an authoritative, peer-reviewed Open Access journal focusing on cardiovascular and cerebrovascular disease. JAHA provides a global forum for basic and clinical research and timely reviews on cardiovascular disease and stroke. As an Open Access journal, its content is free on publication to read, download, and share, accelerating the translation of strong science into effective practice.
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