无循环DNA与心肌梗死:从诊断前景到临床转化

IF 2.1 Q3 PERIPHERAL VASCULAR DISEASE
Jeff Clyde G. Corpuz
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引用次数: 0

摘要

这篇文章回应了Rafiei等人关于游离循环DNA (cfDNA)作为早期检测心肌梗死(MI)的生物标志物的综述。CfDNA显示出快速诊断和实时监测的潜力,但主要障碍仍然存在。缺乏标准化的检测方法,急诊护理的效用不确定,以及高昂的费用,有可能推迟采用和扩大卫生不公平现象,特别是在低收入和中等收入国家。关键优先事项包括协调实验室方案,开发护理点平台,以及将cfDNA整合到心脏肌钙蛋白和心电图(ECG)的诊断算法中。研究应侧重于包括不同人群的大型长期队列,并测试将cfDNA与microrna和DNA甲基化谱结合起来的多标记策略。确保可负担性和可获得性对于将cfDNA从实验承诺转化为常规心血管实践至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating-free DNA and myocardial infarction: From diagnostic promise to clinical translation
This correspondence responds to the review by Rafiei et al. on circulating-free DNA (cfDNA) as a biomarker for early detection of myocardial infarction (MI). CfDNA shows potential for rapid diagnosis and real-time monitoring, but major barriers remain. Lack of standardized testing methods, uncertain utility in emergency care, and high costs risk delaying adoption and widening health inequities, particularly in low- and middle-income countries (LMICs). Key priorities include harmonizing laboratory protocols, developing point-of-care platforms, and integrating cfDNA into diagnostic algorithms with cardiac troponins and electrocardiograms (ECG). Research should focus on large, long-term cohorts that include diverse populations, and test multi-marker strategies combining cfDNA with microRNAs and DNA methylation profiles. Ensuring affordability and accessibility will be critical to translate cfDNA from experimental promise to routine cardiovascular practice.
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