Epigenetic Mechanisms in Heart Diseases.

IF 1.3 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Reviews in cardiovascular medicine Pub Date : 2025-07-30 eCollection Date: 2025-07-01 DOI:10.31083/RCM38696
Mustafa Yildiz
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Abstract

Heart diseases (HDs) continue to be among the major diseases that adversely affect human health worldwide, with complex interactions between genetic, environmental, and biochemical factors contributing to their progression. These include coronary heart disease, hypertension, heart failure, vascular calcification, etc. Cardiovascular diseases have been extensively studied in the Framingham Heart Study since 1948, spanning three generations over the past 70 years, and are highly correlated with various factors, including biochemical, environmental, behavioral, and genetic factors. In recent years, epigenetic mechanisms have emerged as crucial regulators of cardiovascular pathology, influencing gene expression without altering the underlying DNA sequence. Moreover, early detection and diagnosis of heart diseases are crucial for improving treatment and prognosis. Recent studies on heart disease have found that the expression of potential candidate genes related to the disease is associated with epigenetic mechanisms. Indeed, abnormal methylation states have been detected in candidate genes that can serve as biomarkers to assess the progression of heart disease. Recent advances in next-generation sequencing techniques have contributed significantly to our understanding of heart diseases, including the role of DNA methylation, adenosine triphosphate (ATP)-dependent chromatin conformation and remodeling, post-translational modifications of histones and non-coding RNAs. Lastly, this review examines the latest discoveries in the epigenetic regulation of heart diseases, highlighting the roles of DNA methyltransferases (DNMTs), histone deacetylases (HDACs), sirtuins (SIRTs), and ten-eleven translocation proteins (TETs). Additionally, this review highlights preclinical therapeutic strategies targeting epigenetic modifiers, offering new avenues for precision medicine in cardiology. Understanding these epigenetic pathways is crucial for developing novel biomarkers and epigenetic-based therapies that aim to reverse maladaptive cardiac remodeling and enhance clinical outcomes.

心脏病的表观遗传机制。
心脏病(hd)仍然是全球范围内对人类健康产生不利影响的主要疾病之一,遗传、环境和生化因素之间的复杂相互作用促进了其发展。这些疾病包括冠心病、高血压、心力衰竭、血管钙化等。弗雷明汉心脏研究(Framingham Heart Study)从1948年开始对心血管疾病进行了广泛的研究,跨越了70多年的三代人,并与多种因素高度相关,包括生化、环境、行为和遗传因素。近年来,表观遗传机制已成为心血管病理的重要调节因子,影响基因表达而不改变潜在的DNA序列。此外,心脏病的早期发现和诊断对于改善治疗和预后至关重要。最近对心脏病的研究发现,与疾病相关的潜在候选基因的表达与表观遗传机制有关。事实上,在候选基因中已经检测到异常甲基化状态,可以作为评估心脏病进展的生物标志物。新一代测序技术的最新进展极大地促进了我们对心脏病的理解,包括DNA甲基化的作用、三磷酸腺苷(ATP)依赖的染色质构象和重塑、组蛋白和非编码rna的翻译后修饰。最后,本文综述了心脏病表观遗传调控的最新发现,重点介绍了DNA甲基转移酶(dnmt)、组蛋白去乙酰化酶(HDACs)、sirtuins (SIRTs)和10 - 11易位蛋白(TETs)的作用。此外,本文综述了针对表观遗传修饰因子的临床前治疗策略,为心脏病学的精准医学提供了新的途径。了解这些表观遗传途径对于开发新的生物标志物和基于表观遗传的治疗方法至关重要,这些疗法旨在逆转适应性不良的心脏重塑和提高临床结果。
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
Reviews in cardiovascular medicine
Reviews in cardiovascular medicine 医学-心血管系统
CiteScore
2.70
自引率
3.70%
发文量
377
审稿时长
1 months
期刊介绍: RCM is an international, peer-reviewed, open access journal. RCM publishes research articles, review papers and short communications on cardiovascular medicine as well as research on cardiovascular disease. We aim to provide a forum for publishing papers which explore the pathogenesis and promote the progression of cardiac and vascular diseases. We also seek to establish an interdisciplinary platform, focusing on translational issues, to facilitate the advancement of research, clinical treatment and diagnostic procedures. Heart surgery, cardiovascular imaging, risk factors and various clinical cardiac & vascular research will be considered.
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