Exploring the Epigenetic Mechanisms Underlying Chronic Diseases: A Comprehensive Review.

IF 4.1 4区 医学 Q2 GENETICS & HEREDITY
Afaf Aldahish, Rajalakshimi Vasudevan, Shaima Y Al Qasim, Malath Saeed Alshahrani, Lujain Khalid Almohsen, Salma Mohammed Alghanoom, Arwa Ali AlQahtani, Wajan Khalid Alshahrani
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Abstract

Epigenetics, the study of heritable changes in gene expression without changes to the DNA sequence, has emerged as an important regulator of disease risk and development. Epigenetic alterations, such as DNA methylation, histone modifications, and non-coding RNAs, act as molecular bridges between genetic predisposition and environmental factors. Understanding these changes is critical for determining the pathophysiology of chronic illnesses. This article looks at the involvement of epigenetic mechanisms in chronic diseases such as cardiovascular disease, obesity, depression, Alzheimer's disease, and diabetes mellitus. The emphasis is on recent epigenetic discoveries, their implications for disease risk assessment, and the prospect of epigenetic-based therapeutics in precision medicine. Epigenome-Wide Association Studies (EWAS) and next-generation sequencing technologies have revealed disease-specific epigenetic patterns, underlining their potential as biomarkers for early detection and risk stratification. Epigenetic changes affect important molecular pathways that control metabolic regulation, neuroplasticity, inflammatory response, and cellular homeostasis. Epigenetic modification-targeting therapies, such as DNA methylation inhibitors, histone deacetylase inhibitors, and RNA-based treatments, have shown promise in preclinical and early clinical trials. Epigenetic research offers a transformational framework for understanding the intricate interplay of genetic and environmental variables in chronic illness etiology. Epigenetic alterations are reversible, which opens up new possibilities for therapeutic intervention and individualized therapy. Future research should concentrate on improving epigenetic biomarkers, determining causal links in disease progression, and incorporating epigenetic findings into clinical practice. The advancement of epigenetic medicines has the potential to transform disease prevention, treatment, and global health policies.

慢性疾病的表观遗传机制研究综述
表观遗传学,研究基因表达的可遗传变化而不改变DNA序列,已成为疾病风险和发展的重要调节因子。表观遗传改变,如DNA甲基化、组蛋白修饰和非编码rna,是遗传易感性和环境因素之间的分子桥梁。了解这些变化对于确定慢性疾病的病理生理学至关重要。本文着眼于慢性疾病的表观遗传机制,如心血管疾病、肥胖、抑郁症、阿尔茨海默病和糖尿病。重点是最近的表观遗传学发现,它们对疾病风险评估的影响,以及精准医学中基于表观遗传学的治疗方法的前景。全表观基因组关联研究(EWAS)和下一代测序技术揭示了疾病特异性表观遗传模式,强调了它们作为早期检测和风险分层的生物标志物的潜力。表观遗传变化影响控制代谢调节、神经可塑性、炎症反应和细胞稳态的重要分子途径。表观遗传修饰靶向治疗,如DNA甲基化抑制剂、组蛋白去乙酰化酶抑制剂和基于rna的治疗,在临床前和早期临床试验中显示出前景。表观遗传学研究为理解慢性疾病病因中遗传和环境变量的复杂相互作用提供了一个转型框架。表观遗传改变是可逆的,这为治疗干预和个性化治疗开辟了新的可能性。未来的研究应集中于改善表观遗传生物标志物,确定疾病进展的因果关系,并将表观遗传研究结果纳入临床实践。表观遗传药物的进步有可能改变疾病的预防、治疗和全球卫生政策。
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来源期刊
Current gene therapy
Current gene therapy 医学-遗传学
CiteScore
6.70
自引率
2.80%
发文量
46
期刊介绍: Current Gene Therapy is a bi-monthly peer-reviewed journal aimed at academic and industrial scientists with an interest in major topics concerning basic research and clinical applications of gene and cell therapy of diseases. Cell therapy manuscripts can also include application in diseases when cells have been genetically modified. Current Gene Therapy publishes full-length/mini reviews and original research on the latest developments in gene transfer and gene expression analysis, vector development, cellular genetic engineering, animal models and human clinical applications of gene and cell therapy for the treatment of diseases. Current Gene Therapy publishes reviews and original research containing experimental data on gene and cell therapy. The journal also includes manuscripts on technological advances, ethical and regulatory considerations of gene and cell therapy. Reviews should provide the reader with a comprehensive assessment of any area of experimental biology applied to molecular medicine that is not only of significance within a particular field of gene therapy and cell therapy but also of interest to investigators in other fields. Authors are encouraged to provide their own assessment and vision for future advances. Reviews are also welcome on late breaking discoveries on which substantial literature has not yet been amassed. Such reviews provide a forum for sharply focused topics of recent experimental investigations in gene therapy primarily to make these results accessible to both clinical and basic researchers. Manuscripts containing experimental data should be original data, not previously published.
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