Roadmap for translating results from the micronucleus assay into clinical practice: From observational studies to randomized controlled trials

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Reviews in Mutation Research Pub Date : 2021-07-01 DOI:10.1016/j.mrrev.2021.108390
Stefano Bonassi , Michael Fenech
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引用次数: 3

Abstract

According to the definition delivred by the WHO, a biomarker, independently from its role that may be indicative of exposure, response or effect, is inevitably linked to a clinical outcome or to a disease. The presence of a continuum from early biological events to therapy, and prognosis is the unifying mechanism that justifies this conclusion. Traditionally, the technical and inter-individual variability of the assays, together with the long duration between early pathogenetic events and the disease, prevented clinical applications to these biomarkers. These limitations became less important with the emerging of personalized preventive medicine because of the focus on disease prediction and prevention, and the recommended use of all data concerning measurable patient's features. Several papers have been published on the best validation procedures for translating biomarkers to real life. The history of cholesterol concentration is extensively discussed as a reliable example of a biomarker that - after a long and controversial validation process - is currently used in clinical practice. The frequency of micronucleated cells is a reliable biomarker for the pathogenesis of cancer and other non-communicable diseases, and the link with clinical outcomes is substantiated by epidemiological evidence and strong mechanistic basis. Available literature concerning the use of the micronucleus assay in clinical studies is discussed, and a suitable three-levels road-map driving this biomarker towards clinical practice is presented. Under the perspective of personalized medicine, the use of the micronucleus assays can play a decisive role in addressing preventive and therapeutic strategies of chronic diseases. In many cases the MN assay is either currently used in clinical practice or classified as adequate to consider translation into practice. The roadmap to clinical validation of the micronucleus assay finds inspiration from the history of biomarkers such as cholesterol, which clearly showed that the evidence from prospective studies or RCTs is critical to achieve the required level of trust from the healthcare profession. (307 words)

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将微核检测结果转化为临床实践的路线图:从观察性研究到随机对照试验
根据世卫组织提供的定义,生物标志物,独立于其可能指示暴露、反应或影响的作用,不可避免地与临床结果或疾病联系在一起。从早期生物事件到治疗和预后的连续统一体的存在是证明这一结论的统一机制。传统上,检测的技术和个体间差异,以及早期发病事件和疾病之间的长时间,阻碍了这些生物标志物的临床应用。随着个性化预防医学的出现,这些限制变得不那么重要了,因为重点是疾病预测和预防,并建议使用所有有关可测量患者特征的数据。已经发表了几篇关于将生物标志物转化为现实生活的最佳验证程序的论文。胆固醇浓度的历史被广泛讨论,作为一种生物标志物的可靠例子,经过漫长而有争议的验证过程,目前已用于临床实践。微核细胞的频率是癌症和其他非传染性疾病发病机制的可靠生物标志物,其与临床结果的联系得到流行病学证据和强有力的机制基础的证实。关于在临床研究中使用微核测定的现有文献进行了讨论,并提出了一个合适的三级路线图,推动这种生物标志物走向临床实践。在个性化医疗的视角下,微核检测的应用可以在制定慢性病的预防和治疗策略方面发挥决定性作用。在许多情况下,锰含量测定要么目前用于临床实践,要么被归类为足以考虑转化为实践。微核检测的临床验证路线图从胆固醇等生物标志物的历史中获得灵感,这清楚地表明,前瞻性研究或随机对照试验的证据对于获得医疗保健专业人员所需的信任水平至关重要。(307字)
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来源期刊
CiteScore
12.20
自引率
1.90%
发文量
22
审稿时长
15.7 weeks
期刊介绍: The subject areas of Reviews in Mutation Research encompass the entire spectrum of the science of mutation research and its applications, with particular emphasis on the relationship between mutation and disease. Thus this section will cover advances in human genome research (including evolving technologies for mutation detection and functional genomics) with applications in clinical genetics, gene therapy and health risk assessment for environmental agents of concern.
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