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表观遗传年龄与脑部健康事件之间的双向关系。

Bidirectional relationship between epigenetic age and brain health events.

作者信息

Rivier Cyprien, Szejko Natalia, Renedo Daniela, Clocchiatti-Tuozzo Santiago, Huo Shufan, de Havenon Adam, Zhao Hongyu, Gill Thomas, Sheth Kevin, Falcone Guido

机构信息

Yale School of Medicine.

Medical University of Warsaw.

出版信息

Res Sq. 2024 Jun 25:rs.3.rs-4378855. doi: 10.21203/rs.3.rs-4378855/v1.

Abstract

Chronological age offers an imperfect estimate of the molecular changes that occur with aging. Epigenetic age, which is derived from DNA methylation data, provides a more nuanced representation of aging-related biological processes. This study examines the bidirectional relationship between epigenetic age and the occurrence of brain health events (stroke, dementia, and late-life depression). Using data from the Health and Retirement Study, we analyzed blood samples from over 4,000 participants to determine how epigenetic age relates to past and future brain health events. Study participants with a prior brain health event prior to blood collection were 4% epigenetically older (beta 0.04, SE 0.01), suggesting that these conditions are associated with faster aging than that captured by chronological age. Furthermore, a one standard deviation increase in epigenetic age was associated with 70% higher odds of experiencing a brain health event in the next four years after blood collection (OR 1.70, 95%CI 1.16-2.50), indicating that epigenetic age is not just a consequence but also a predictor of poor brain health. Both results were replicated through Mendelian Randomization analyses, supporting their causal nature. Our findings support the utilization of epigenetic age as a useful biomarker to evaluate the role of interventions aimed at preventing and promoting recovery after a brain health event.

摘要

实足年龄对衰老过程中发生的分子变化的估计并不完美。基于DNA甲基化数据得出的表观遗传年龄,能更细致地反映与衰老相关的生物学过程。本研究考察了表观遗传年龄与脑健康事件(中风、痴呆和晚年抑郁症)发生之间的双向关系。利用健康与退休研究的数据,我们分析了4000多名参与者的血样,以确定表观遗传年龄与过去和未来脑健康事件之间的关系。在采血前有过脑健康事件的研究参与者,其表观遗传年龄要大4%(β=0.04,标准误=0.01),这表明这些疾病与比实足年龄所反映的更快的衰老有关。此外,表观遗传年龄每增加一个标准差,在采血后的未来四年内发生脑健康事件的几率就会高出70%(比值比=1.70,95%置信区间=1.16 - 2.50),这表明表观遗传年龄不仅是脑健康状况不佳的结果,也是其预测指标。两项结果均通过孟德尔随机化分析得到了验证,支持了它们的因果关系本质。我们的研究结果支持将表观遗传年龄用作一种有用的生物标志物,以评估旨在预防脑健康事件及促进其恢复后康复的干预措施的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ad5/11230493/1c70f35052dc/nihpp-rs4378855v1-f0001.jpg

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