Mitochondrial medicine: "from bench to bedside" 3PM-guided concept.

IF 5.9 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
The EPMA journal Pub Date : 2025-04-15 eCollection Date: 2025-06-01 DOI:10.1007/s13167-025-00409-4
Qianwen Shao, Marie Louise Ndzie Noah, Olga Golubnitschaja, Xianquan Zhan
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引用次数: 0

Abstract

Mitochondria are the primary sites for aerobic respiration and play a vital role in maintaining physiologic function at the cellular and organismal levels. Physiologic mitochondrial homeostasis, functions, health, and any kind of mitochondrial impairments are associated with systemic effects that are linked to the human health and pathologies. Contextually, mitochondria are acting as a natural vital biosensor in humans controlling status of physical and mental health in a holistic manner. So far, no any disorder is known as happening to humans independently from a compromised mitochondrial health as the cause (primary mitochondrial dysfunction) or a target of collateral damage (secondary mitochondrial injury). This certainty makes mitochondrial medicine be the superior instrument to reach highly ambitious objectives of predictive, preventive, and personalized medicine (PPPM/3PM). 3PM effectively implements the paradigm change from the economically ineffective reactive medical services to a predictive approach, targeted prevention and treatments tailored to individualized patient profiles in primary (protection against health-to-disease transition) and secondary (protection against disease progression) healthcare. Mitochondrial DNA (mtDNA) properties differ significantly from those of nuclear DNA (nDNA). For example, mtDNA as the cell-free DNA molecule is much more stable compared to nDNA, which makes mtDNA be an attractive diagnostic target circulating in human body fluids such as blood and tear fluid. Further, genetic variations in mtDNA contribute to substantial individual differences in disease susceptibility and treatment response. To this end, the current gene editing technologies, such as clustered regularly interspaced short palindromic repeats (CRISPR)/Cas, are still immature in mtDNA modification, and cannot be effectively applied in clinical practice posing a challenge for mtDNA-based therapies. In contrast, comprehensive multiomics technologies offer new insights into mitochondrial homeostasis, health, and functions, which enables to develop more effective multi-level diagnostics and targeted treatment strategies. This review article highlights health- and disease-relevant mitochondrial particularities and assesses involvement of mitochondrial medicine into implementing the 3PM objectives. By discussing the interrelationship between 3PM and mitochondrial medicine, we aim to provide a foundation for advancing early and predictive diagnostics, cost-effective targeted prevention in primary and secondary care, and exemplify personalized treatments creating proof-of-concept approaches for 3PM-guided clinical applications.

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线粒体医学:“从实验室到病床”的3pm指导概念。
线粒体是有氧呼吸的主要部位,在维持细胞和有机体水平的生理功能方面起着至关重要的作用。生理性线粒体稳态、功能、健康和任何种类的线粒体损伤都与与人类健康和病理相关的全身效应有关。在此背景下,线粒体作为一种天然的重要生物传感器,在人类整体控制身体和心理健康状态。到目前为止,还没有一种疾病是独立于线粒体健康受损的原因(原发性线粒体功能障碍)或附带损伤的目标(继发性线粒体损伤)而发生在人类身上的。这种确定性使线粒体医学成为实现预测、预防和个性化医疗(PPPM/3PM)这一雄心勃勃的目标的优越工具。3PM有效地实现了从经济上无效的反应性医疗服务到预测性方法的范式转变,在初级(防止健康向疾病过渡)和二级(防止疾病进展)医疗保健中针对个性化患者的针对性预防和治疗。线粒体DNA (mtDNA)的性质与核DNA (nDNA)有很大的不同。例如,作为游离DNA分子的mtDNA比nDNA稳定得多,这使得mtDNA成为血液和泪液等体液中循环的有吸引力的诊断靶点。此外,mtDNA的遗传变异有助于疾病易感性和治疗反应的实质性个体差异。因此,目前的基因编辑技术,如聚集规律间隔短回文重复序列(CRISPR)/Cas,在mtDNA修饰方面还不成熟,无法有效应用于临床实践,这对基于mtDNA的治疗提出了挑战。相比之下,综合多组学技术为线粒体稳态、健康和功能提供了新的见解,从而能够开发更有效的多层次诊断和靶向治疗策略。这篇综述文章强调了与健康和疾病相关的线粒体特殊性,并评估了线粒体医学在实现3PM目标中的作用。通过讨论3PM与线粒体医学之间的相互关系,我们的目标是为推进早期和预测性诊断,在初级和二级医疗中具有成本效益的针对性预防提供基础,并举例说明个性化治疗,为3PM指导的临床应用创造概念验证方法。
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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CiteScore
12.50
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