Molecular prevention of chronic non-communicable diseases: How close are we?

T. Pekmezović
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Abstract

Chronic non-communicable diseases (CNDs) are a leading cause of death worldwide; preterm mortality in people younger than 70 years accounts for 40% of the total of 38 million deaths due to CNDs. Heterogeneity and complexity of CNDs cause shifting the prevention focus towards the molecular level in order to contribute to the global decrease of disease burden. Given that fact, the aims of molecular prevention are determination of crucial genetic, epigenetic and environmental factors that influence different responses to agents, as well as those that modify responses to agent exposure and tendency of development of chronic diseases. Also, it is important to mention the recognition of new pathways of pharmacologic modulation. Although basic postulates of molecular preventions are still at their beginning, the fact that significant results in the field of clarifying CNDs etiology and early pathogenesis, risk assessment and modeling, as well as targeting of agents with high preventable efficacy have already been achieved, it is clear that there is a possibility to decrease CNDs burden in the earliest phases of its natural course. Accordingly, it is important to change the belief that a person without clinical symptoms and signs of disease is necessarily healthy. On the other hand, there is a need to balance the risks and health; molecular prevention has its own place in that interspace. Studies investigating the effects of potential preventive measures at molecular level have clearly determined high-risk cohorts, outcomes and other design elements, similarly to clinical studies. There is an intensive development of new research fields, like nutrigenomics which investigates the impact of diet on metabolic pathways and homeostasis, that is, their regulation in early stages of diseases associated with nutrition, as well as the level of susceptibility of person with certain genotype to those diseases. The investigations in the fields of molecular prevention may contribute to new biomarkers development or help the setting of strategies for CNDs molecular prevention and nanotherapy. In other words, they represent the marker of genomics applying in population sciences.
慢性非传染性疾病的分子预防:我们离目标还有多远?
慢性非传染性疾病(CNDs)是全世界的一个主要死亡原因;70岁以下人群的早产死亡率占由心血管疾病导致的3800万死亡总数的40%。CNDs的异质性和复杂性导致预防重点转向分子水平,以促进全球疾病负担的减少。鉴于这一事实,分子预防的目的是确定影响对病原体的不同反应的关键遗传、表观遗传和环境因素,以及那些改变对病原体接触的反应和慢性疾病发展趋势的因素。此外,重要的是要提到认识新的途径的药理调节。尽管分子预防的基本假设仍处于起步阶段,但在阐明CNDs的病因和早期发病机制、风险评估和建模以及靶向具有高预防功效的药物方面已经取得了重大成果,显然有可能在其自然过程的早期阶段减轻CNDs的负担。因此,重要的是要改变没有临床症状和疾病迹象的人一定是健康的信念。另一方面,有必要平衡风险和健康;分子预防在这个空间中占有一席之地。与临床研究类似,在分子水平上调查潜在预防措施效果的研究明确确定了高危人群、结局和其他设计要素。新的研究领域正在密集发展,如营养基因组学,它研究饮食对代谢途径和体内平衡的影响,即它们在与营养有关的疾病的早期阶段的调节,以及具有某些基因型的人对这些疾病的易感性水平。分子预防领域的研究可能有助于开发新的生物标志物或帮助制定CNDs分子预防和纳米治疗策略。换句话说,它们代表了基因组学在人口科学中应用的标志。
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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