A novel framework to build saliva-based DNA methylation biomarkers: Quantifying systemic chronic inflammation as a case study

IF 7.8 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Aging Cell Pub Date : 2025-01-30 DOI:10.1111/acel.14444
Lisa J. Schmunk, Toby P. Call, Daniel L. McCartney, Hira Javaid, Waylon J. Hastings, Vanja Jovicevic, Dragoljub Kojadinović, Natacha Tomkinson, Eliska Zlamalova, Kirsty C. McGee, Jack Sullivan, Archie Campbell, Andrew M. McIntosh, Veronika Óvári, Karl Wishart, Christian E. Behrens, Emma Stone, Miloš Gavrilov, Rob Thompson, Hurdle bio-infrastructure team, Thomas Jackson, Janet M. Lord, Thomas M. Stubbs, Riccardo E. Marioni, Daniel E. Martin-Herranz
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Abstract

Accessible and non-invasive biomarkers that measure human ageing processes and the risk of developing age-related disease are paramount in preventative healthcare. Here, we describe a novel framework to train saliva-based DNA methylation (DNAm) biomarkers that are reproducible and biologically interpretable. By leveraging a reliability dataset with replicates across tissues, we demonstrate that it is possible to transfer knowledge from blood DNAm to saliva DNAm data using DNAm proxies of blood proteins (EpiScores). We apply these methods to create a new saliva-based epigenetic clock (InflammAge) that quantifies systemic chronic inflammation (SCI) in humans. Using a large blood DNAm human cohort with linked electronic health records and over 18,000 individuals (Generation Scotland), we demonstrate that InflammAge significantly associates with all-cause mortality, disease outcomes, lifestyle factors, and immunosenescence; in many cases outperforming the widely used SCI biomarker C-reactive protein (CRP). We propose that our biomarker discovery framework and InflammAge will be useful to improve understanding of the molecular mechanisms underpinning human ageing and to assess the impact of gero-protective interventions.

Abstract Image

构建基于唾液的DNA甲基化生物标志物的新框架:量化全身性慢性炎症作为案例研究。
测量人类衰老过程和发展与年龄相关疾病风险的可获取和非侵入性生物标志物在预防性医疗保健中至关重要。在这里,我们描述了一个新的框架来训练基于唾液的DNA甲基化(DNAm)生物标志物,这些生物标志物是可重复的和生物可解释的。通过利用跨组织复制的可靠性数据集,我们证明可以使用血液蛋白的DNAm代理(EpiScores)将知识从血液DNAm转移到唾液DNAm数据。我们应用这些方法来创建一个新的基于唾液的表观遗传时钟(炎症),量化人类的系统性慢性炎症(SCI)。通过使用具有相关电子健康记录的大型血液DNAm人类队列和超过18,000个人(苏格兰一代),我们证明了炎症与全因死亡率、疾病结局、生活方式因素和免疫衰老显著相关;在许多情况下优于广泛使用的SCI生物标志物c反应蛋白(CRP)。我们提出,我们的生物标志物发现框架和炎症将有助于提高对人类衰老分子机制的理解,并评估老年保护干预措施的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
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