Environmental Epigenetics and Its Impacts on Disease Susceptibility: A Comprehensive Review

Taiwo Temitope Ogunjobi, T. Gbayisomore, Patrica Okwuchi Nneji, O. Olofin, Emmanuel Niyi Olowe, Chimaobi Divine Gigam-Ozuzu, Jolayemi Ibidunni Afolabi, Ngozi Benedette Okwuokei, Victor Abiodun Boluwaji, Taiwo Paul Ojeniran, I. O. Ogini, Seth Olorunmijuwomlo Adesope, T. D. Yissa, Cyril Arinze Eji
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Abstract

Environmental epigenetics, an emerging field, investigates the interplay between environmental factors and epigenetic changes, shaping an individual's disease vulnerability. This review highlights the associations among genetics, environment, and health. Environmental epigenetics significantly impacts disease susceptibility through mechanisms like non-coding RNAs, histone modifications, and DNA methylation, responding to external stimuli and dynamically interacting with genes. Lifelong epigenetic imprints, influenced by the prenatal environment, early experiences, diet, chemical exposures, and lifestyle, dictate health trajectories across the lifespan, elevating the risk of various illnesses, including cancer, cardiovascular, metabolic, and neurological conditions. Major findings demonstrate how antenatal environmental factors—like mother's diet, food and stress level—shape fetal epigenetic programming and impact health consequences in the future. Furthermore, it has been demonstrated that environmental pollutants and dietary nutrients can modify epigenetic markers, highlighting the crucial role that lifestyle decisions have in reducing the risk of disease. Significantly, the notion that epigenetic alterations may be passed down through generations raises the possibility that environmental exposures may have an impact on health consequences for future generations. Environmental epigenetics revolutionizes our understanding of gene-environment interactions and their role in disease etiology. The study concludes by highlighting the revolutionary implications of environmental epigenetics for comprehending the etiology of disease and customizing public health approaches, and by promoting the incorporation of both genetic and environmental components within public health frameworks. The knowledge acquired calls for an evolution of paradigms in medicine toward customized care utilizing epigenetic biomarkers and calls for more studies to improve therapies that lessen the harmful epigenetic consequences of exposure to the environment.
环境表观遗传学及其对疾病易感性的影响:全面回顾
环境表观遗传学是一个新兴领域,研究环境因素与表观遗传变化之间的相互作用,从而影响个人的疾病易感性。本综述强调了遗传、环境和健康之间的关联。环境表观遗传学通过非编码 RNA、组蛋白修饰和 DNA 甲基化等机制对疾病易感性产生重大影响,对外界刺激做出反应,并与基因发生动态交互作用。受产前环境、早期经历、饮食、化学接触和生活方式影响的终生表观遗传印记决定了整个生命周期的健康轨迹,增加了罹患各种疾病的风险,包括癌症、心血管疾病、代谢疾病和神经系统疾病。主要研究结果表明,产前环境因素(如母亲的饮食、食物和压力水平)如何塑造胎儿的表观遗传程序并影响未来的健康后果。此外,研究还表明,环境污染物和膳食营养成分可改变表观遗传标记,这凸显了生活方式决定在降低疾病风险方面的关键作用。重要的是,表观遗传学改变可能会代代相传,这就提出了环境暴露可能会对后代健康产生影响的可能性。环境表观遗传学彻底改变了我们对基因与环境相互作用及其在疾病病因学中作用的认识。本研究最后强调了环境表观遗传学对理解疾病病因学和定制公共卫生方法的革命性影响,并推动将遗传和环境因素纳入公共卫生框架。所获得的知识要求医学范式向利用表观遗传生物标志物进行定制化护理的方向发展,并要求开展更多研究,以改进疗法,减轻暴露于环境中对表观遗传造成的有害影响。
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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