鉴定心肾代谢性疾病DNA甲基化标志物的新方法及应用。

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY
Epigenomics Pub Date : 2025-10-01 Epub Date: 2025-08-12 DOI:10.1080/17501911.2025.2540273
Chang Liu, Alexandra Young, Nanzha Abi, Junyu Chen, Matheus Fernandes Gyorfy, Yanping Li, Sophia Sun, Jin J Zhou, Yan V Sun
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引用次数: 0

摘要

心肾代谢性疾病是一项重大的公共卫生挑战,在全球发病率和死亡率负担中占很大比例。这些疾病有共同的风险因素,包括遗传易感性、环境暴露和生活方式影响,这些因素共同推动疾病的发展和进展。表观遗传修饰,特别是DNA甲基化(DNAm),通过在不改变DNA序列的情况下调节基因表达,在这些危险因素和疾病表型之间充当关键的介质和生物标志物。全表观基因组关联研究已经确定了与CKM疾病和相关表型相关的dna标记,强调了炎症、代谢功能障碍和衰老相关过程中的共享途径和疾病特异性表观遗传特征。纵向研究进一步证明了DNAm随时间变化的动态性质,为疾病轨迹提供了见解。此外,整合多种表观遗传标记的甲基化风险评分在改善疾病预测和风险分层方面表现出超越传统临床因素的希望。为了综合目前的证据,我们在PubMed上进行了一项有针对性的文献检索,检索2014年至今发表的英语、同行评议的文章。未来的研究利用大规模、表型良好的队列、先进的统计方法和创新的研究设计,对于发现新的生物标志物、完善风险预测模型和开发靶向表观遗传疗法来减轻全球负担至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel approaches and applications in identifying DNA methylation markers of cardio-kidney-metabolic disease.

Cardio-kidney-metabolic (CKM) diseases represent a major public health challenge, accounting for a large proportion of global burden of morbidity and mortality. These conditions share risk factors, including genetic predisposition, environmental exposures, and lifestyle influences, which collectively drive disease development and progression. Epigenetic modifications, particularly DNA methylation (DNAm), serve as key mediators and biomarkers between these risk factors and disease phenotypes by regulating gene expression without altering the DNA sequence. Epigenome-wide association studies have identified DNAm markers associated with CKM diseases and related phenotypes, highlighting both shared pathways and disease-specific epigenetic signatures in inflammation, metabolic dysfunction, and aging-related processes. Longitudinal studies further demonstrate the dynamic nature of DNAm changes over time, offering insights into disease trajectories. Additionally, methylation risk scores integrating multiple epigenetic markers show promise in improving disease prediction and risk stratification beyond traditional clinical factors. To synthesize the current evidence, we conducted a targeted literature search in PubMed for English-language, peer-reviewed articles published between 2014 and the present. Future research leveraging large, well-phenotyped cohorts, advanced statistical methods, and innovative study designs will be critical for uncovering novel biomarkers, refining risk prediction models, and developing targeted epigenetic therapies to mitigate the global burden.

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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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