关键词: aging biomarker cell-free DNA epigenetic clock inflamm-aging methylation

Mesh : Humans DNA Methylation Aging / genetics Cell-Free Nucleic Acids / blood genetics Female Inflammation / genetics Male CpG Islands Aged Middle Aged Epigenesis, Genetic Adult Biomarkers / blood Aged, 80 and over

来  源:   DOI:10.1080/17501911.2024.2340958   PDF(Pubmed)

Abstract:
Aim: Liquid biopsies analyzing cell-free DNA (cfDNA) methylation in plasma offer a noninvasive diagnostic for diseases, with the potential of aging biomarkers underexplored. Methods: Utilizing enzymatic methyl-seq (EM-seq), this study assessed cfDNA methylation patterns in aging with blood from 35 healthy individuals. Results: It found aging signatures, including higher cfDNA levels and variations in fragment sizes, plus approximately 2000 age-related differentially methylated CpG sites. A biological age predictive model based on 48 CpG sites showed a strong correlation with chronological age, verified by two datasets. Age-specific epigenetic shifts linked to inflammation were revealed through differentially methylated regions profiling and Olink proteomics. Conclusion: These findings suggest cfDNA methylation as a potential aging biomarker and might exacerbate immunoinflammatory reactivity in older individuals.
Our bodies undergo many changes as we age, some of which might affect our health. To better understand these changes, scientists study something called ‘cell-free DNA\' (cfDNA) in our blood. This cfDNA can give us clues about our health and the risk of diseases like cancer or heart conditions.In our research, we analyzed cfDNA from the blood of 35 people to identify patterns associated with aging. We discovered that approximately 2000 specific spots in our DNA change in a way that\'s linked to aging. These changes might help us figure out someone\'s biological age – essentially, how old their body seems based on various health factors, which can differ from their actual age.We also found that these DNA changes could indicate how aging might make the body\'s defense system – which fights off diseases – react more intensely. Understanding this could be crucial for managing health as we get older.Our study suggests that cfDNA could be a useful marker for aging, offering a new approach to understanding and possibly managing the health effects associated with growing older.
摘要:
目的:分析血浆中无细胞DNA(cfDNA)甲基化的液体活检为疾病提供非侵入性诊断,随着潜在的衰老生物标志物的开发不足。方法:利用酶促甲基-seq(EM-seq),这项研究评估了35名健康个体的血液老化中的cfDNA甲基化模式。结果:它发现了衰老特征,包括更高的cfDNA水平和片段大小的变化,加上大约2000个与年龄相关的差异甲基化CpG位点。基于48个CpG位点的生物年龄预测模型与实际年龄有很强的相关性,由两个数据集验证。通过差异甲基化区域分析和Olink蛋白质组学揭示了与炎症相关的年龄特异性表观遗传变化。结论:这些发现表明cfDNA甲基化是一种潜在的衰老生物标志物,可能会加剧老年人的免疫炎症反应。
随着年龄的增长,我们的身体会发生许多变化,其中一些可能会影响我们的健康。为了更好地理解这些变化,科学家在我们的血液中研究一种叫做“无细胞DNA”(cfDNA)的东西。这种cfDNA可以为我们提供有关健康和癌症或心脏病等疾病风险的线索。在我们的研究中,我们分析了35人血液中的cfDNA,以确定与衰老相关的模式。我们发现,在我们的DNA中大约有2000个特定的斑点以一种与衰老有关的方式发生变化。这些变化可能会帮助我们弄清楚某人的生物年龄-本质上,根据各种健康因素,他们的身体看起来有多大,这可能与他们的实际年龄不同。我们还发现,这些DNA变化可能表明衰老可能使身体的防御系统-抵抗疾病-反应更强烈。随着年龄的增长,了解这一点对于管理健康至关重要。我们的研究表明,cfDNA可能是衰老的有用标记,提供了一种新的方法来理解并可能管理与年龄增长相关的健康影响。
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