Nour Zeinab, El-Hamamsy Kariman, Ehsan Iman, Fawaz Lobna, Shaker Olfat, Mossallam Dalia, ElGindy Hala
Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Department of Pediatrics, Faculty of Medicine Cairo University, Egypt.
Rep Biochem Mol Biol. 2022 Jul;11(2):327-335. doi: 10.52547/rbmb.11.2.327.
Sepsis is one of the most common causes of multiorgan failure. Sepsis requires the presence of infection with a resultant systemic inflammatory state. Organ dysfunction occurs from the combination of the two processes. Sepsis is the main cause of mortality at intensive care units, with 30-50% mortality rate for all septic episodes. MicroRNA (miRNA) profile data could be beneficial as a specific diagnostic biomarker for sepsis and systemic inflammatory response syndrome (SIRS).
Expression of miRNAs -122, -181b, -223 and -146a levels were assayed by quantitative real time polymerase chain reaction (qRT-PCR) in a prospective case control study, where forty septic cases were compared to 40 healthy controls of matched age and gender.
miRNAs -122 and -181b were significantly upregulated during early septic conditions, indicating that they could be sensitive and specific biomarkers for diagnosing sepsis. miRNA-223 and miRNA-146a could also represent highly specific and sensitive diagnostic biomarkers, as they were found to be significantly down-regulated. Serum levels of miRNA-223 could be used to predict poor prognosis with 70% sensitivity and 75% specificity, whereas the other three miRNAs could not predict prognosis.
Our study shows that all tested miRNAs can be used for early detection of sepsis, with miRNA-223 being predictive of mortality, hence preventing multi-organ failure and reducing mortality, and predicting poor outcomes, thereby assisting in early categorization of ICU patients for rapid appropriate treatment and medico legal aspects.
脓毒症是多器官功能衰竭最常见的病因之一。脓毒症需要存在感染并伴有全身性炎症状态。器官功能障碍是这两个过程共同作用的结果。脓毒症是重症监护病房死亡的主要原因,所有脓毒症发作的死亡率为30%-50%。微小RNA(miRNA)谱数据作为脓毒症和全身炎症反应综合征(SIRS)的特异性诊断生物标志物可能会有所帮助。
在一项前瞻性病例对照研究中,通过定量实时聚合酶链反应(qRT-PCR)检测了miRNAs -122、-181b、-223和-146a的表达水平,将40例脓毒症患者与40例年龄和性别匹配的健康对照进行了比较。
在脓毒症早期,miRNAs -122和-181b显著上调,表明它们可能是诊断脓毒症的敏感且特异的生物标志物。miRNA-223和miRNA-146a也可能是高度特异和敏感的诊断生物标志物,因为它们被发现显著下调。miRNA-223的血清水平可用于预测不良预后,敏感性为70%,特异性为75%,而其他三种miRNA不能预测预后。
我们的研究表明,所有检测的miRNA均可用于脓毒症的早期检测,其中miRNA-223可预测死亡率,从而预防多器官功能衰竭并降低死亡率,还可预测不良结局,从而有助于对重症监护病房患者进行早期分类,以便进行快速适当的治疗以及处理医疗法律方面问题。