揭示dna甲基化年龄加速对糖尿病和糖尿病前期死亡风险的影响:来自美国NHANES项目的见解。

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
Shuang Wu, Ziyi Zhong, Yimeng Wang, Jingyang Wang, Siqi Lyu, Hongyu Liu, Yang Chen
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引用次数: 0

摘要

背景:糖尿病是全球第九大死亡原因,dna甲基化年龄加速(DNAmAA)与寿命密切相关。然而,DNAmAA对糖尿病和糖尿病前期特定人群长期预后的影响尚未得到全面研究。方法:这项回顾性队列研究利用1999-2002年国家健康与营养调查(NHANES)的数据,包括20岁或以上诊断为糖尿病或糖尿病前期的参与者。DNAmAA定义为表观遗传年龄与实足年龄之差。包括多代DNAmAA测量。采用Cox比例风险回归模型估计DNAmAAs与全因死亡率、心血管死亡率和非心血管死亡率之间的关系。结果:共纳入1199名受试者,平均年龄64.20(0.46)岁;男性621例(51.8%)。在糖尿病和糖尿病前期组中,实足年龄和所有dna甲基化年龄之间观察到显著的相关性。在平均14.13(5.90)年的随访中,记录了662例死亡。AgeAccelGrim2与死亡率的相关性最强。AgeAccelGrim2每增加5个单位与全因死亡率(HR 1.35, 95% CI 1.23-1.49)、心血管死亡率(HR 1.50, 95% CI 1.25-1.80)和非心血管死亡率(HR 1.30, 95% CI 1.16-1.46)升高相关。这些关联在糖尿病和糖尿病前期患者中仍然显著。中介分析显示,AgeAccelGrim2在糖尿病和糖尿病前期人群中显著调节健康相关暴露(包括氧化平衡评分、生活简单7评分和虚弱评分)与全因死亡率之间的关联。结论:AgeAccelGrim2可作为糖尿病和糖尿病前期人群特异性死亡风险的有价值的生物标志物,在个性化管理策略和风险分层方面具有潜在的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the impact of DNA-methylation age acceleration on mortality risk in diabetes and pre-diabetes: insights from the US NHANES program.

Background: Diabetes ranks as the ninth leading cause of death globally, and DNA-methylation age acceleration (DNAmAA) is closely linked to lifespan. However, the impact of DNAmAA on long-term outcomes in specific populations with diabetes and pre-diabetes has not yet been comprehensively studied.

Methods: This retrospective cohort study utilized data from the National Health and Nutrition Examination Survey (NHANES) 1999-2002, including participants aged 20 years or older diagnosed with diabetes or pre-diabetes. DNAmAA was defined as the difference between epigenetic age and chronological age. Multiple generations of DNAmAA measures were included. Cox proportional hazards regression models were employed to estimate the associations between DNAmAAs and all-cause, cardiovascular, and non-cardiovascular mortality.

Results: A total of 1,199 participants were included, with a mean age of 64.20 (0.46) years; 621 (51.8%) were male. Significant correlations were observed between chronological age and all DNA-methylation ages in both diabetes and pre-diabetes groups. Over a mean follow-up of 14.13 (5.90) years, 662 deaths were recorded. AgeAccelGrim2 exhibited the strongest association with mortality. Each 5-unit increase in AgeAccelGrim2 was associated with an elevated risk of all-cause mortality (HR 1.35, 95% CI 1.23-1.49), cardiovascular mortality (HR 1.50, 95% CI 1.25-1.80), and non-cardiovascular mortality (HR 1.30, 95% CI 1.16-1.46). These associations remained significant in participants with diabetes and pre-diabetes. Mediation analysis revealed that AgeAccelGrim2 significantly mediates the association between health-related exposures (including the Oxidative Balance Score, Life's Simple 7 score, and frailty score) and all-cause mortality in diabetes and pre-diabetes populations.

Conclusions: AgeAccelGrim2 could serve as a valuable biomarker for mortality risk specific to populations with diabetes and pre-diabetes, offering potential applications in personalized management strategies and risk stratification.

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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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