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Circulating microRNAs as potential biomarkers for the early diagnosis of acute myocardial infarction: Promises and challenges

机译:循环microRNA作为急性心肌梗死早期诊断的潜在生物标志物:前景与挑战

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摘要

We read with great interest the letter of Lippi et al., who recently performed a meta-analysis of different circulating microRNAs (miRs), e.g. miR-1, -133, -208, -499 and -663b, describing their sensitivity and specificity in diagnosis of acute myocardial infarction (AMI). In fact, the increased cell-free miRs may not only be a product of plasma membrane disruption following cell death, but also a consequence of an active release from living cells exposed to ischemic condition, thereby it can be hypothesized that circulating cardiac miRs may be earlier biomarkers of myocardial necrosis.A rapid and efficient assessment of AMI is essential because of the reduced mortality rate and prognostic benefit following timely interventions. Nevertheless, early diagnostic evaluation of patients suspected of having AMI remains a challenge, especially when electrocardiogram (ECG) is nondiagnostic. Currently, definitive diagnosis of AMI is mainly based on the elevated biomarkers of damaged cardiomyocytes, cardiac troponin T and I (cTnT and cTnl) or creatinine kinase-MB isoenzyme (CK-MB) if cTn is unavailable, in the context of clinical and ECG findings.
机译:我们非常感兴趣地阅读了Lippi等人的信,他最近对不同的循环microRNA(miRs)(例如miR-1,-133,-208,-499和-663b,描述了它们在诊断急性心肌梗塞(AMI)中的敏感性和特异性。实际上,增加的无细胞miRs可能不仅是细胞死亡后质膜破坏的产物,而且是暴露于缺血状态的活细胞主动释放的结果,因此可以假设循环的心脏miRs可能是心肌坏死的早期生物标志物。快速有效地评估AMI是必不可少的,因为及时采取干预措施可降低死亡率和预后。尽管如此,对怀疑患有AMI的患者进行早期诊断评估仍然是一个挑战,尤其是在心电图(ECG)无法诊断的情况下。目前,对于AMI的明确诊断主要是基于受损的心肌细胞,心肌肌钙蛋白T和I(cTnT和cTnl)或肌酐激酶-MB同工酶(CK-MB)的升高的生物标志物(在临床和ECG的背景下)。发现。

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