Oh Sang Hoon, Kim Ho-Shik, Park Kyu Nam, Ji Sanghee, Park Ji-Young, Choi Seung Pill, Lim Jee Yong, Kim Han Joon
Department of Emergency Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Department of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Diagnostics (Basel). 2021 Oct 15;11(10):1905. doi: 10.3390/diagnostics11101905.
Early prognostication in cardiac arrest survivors is challenging for physicians. Unlike other prognostic modalities, biomarkers are easily accessible and provide an objective assessment method. We hypothesized that in cardiac arrest patients with targeted temperature management (TTM), early circulating microRNA (miRNA) levels are associated with the 6-month neurological outcome. In the discovery phase, we identified candidate miRNAs associated with cardiac arrest patients who underwent TTM by comparing circulating expression levels in patients and healthy controls. Next, using a larger cohort, we validated the prognostic values of the identified early miRNAs by measuring the serum levels of miRNAs, neuron-specific enolase (NSE), and S100 calcium-binding protein B (S100B) 6 h after cardiac arrest. The validation cohort consisted of 54 patients with TTM. The areas under the curve (AUCs) for poor outcome were 0.85 (95% CI (confidence interval), 0.72-0.93), 0.82 (95% CI, 0.70-0.91), 0.78 (95% CI, 0.64-0.88), and 0.77 (95% CI, 0.63-0.87) for miR-6511b-5p, -125b-1-3p, -122-5p, and -124-3p, respectively. When the cut-off was based on miRNA levels predicting poor outcome with 100% specificity, sensitivities were 67.7% (95% CI, 49.5-82.6), 50.0% (95% CI, 32.4-67.7), 35.3% (95% CI, 19.7-53.5), and 26.5% (95% CI, 12.9-44.4) for the above miRNAs, respectively. The models combining early miRNAs with protein biomarkers demonstrated superior prognostic performance to those of protein biomarkers.
对医生来说,心脏骤停幸存者的早期预后评估具有挑战性。与其他预后评估方法不同,生物标志物易于获取,并提供了一种客观的评估方法。我们假设,在接受目标温度管理(TTM)的心脏骤停患者中,早期循环微RNA(miRNA)水平与6个月时的神经学预后相关。在发现阶段,我们通过比较患者和健康对照的循环表达水平,确定了与接受TTM的心脏骤停患者相关的候选miRNA。接下来,我们使用更大的队列,通过在心脏骤停后6小时测量miRNA、神经元特异性烯醇化酶(NSE)和S100钙结合蛋白B(S100B)的血清水平,验证了所确定的早期miRNA的预后价值。验证队列由54例接受TTM的患者组成。对于miR-6511b-5p、-125b-1-3p、-122-5p和-124-3p,不良预后的曲线下面积(AUC)分别为0.85(95%置信区间(CI),0.72 - 0.93)、0.82(95%CI,0.70 - 0.91)、0.78(95%CI,0.64 - 0.88)和0.77(95%CI,0.63 - 0.87)。当以预测不良预后的miRNA水平为基础,设定具有100%特异性的临界值时,上述miRNA的敏感性分别为67.7%(95%CI,49.5 - 82.6)、50.0%(95%CI,32.4 - 67.7)、35.3%(95%CI,19.7 - 53.5)和26.5%(95%CI,12.9 - 44.4)。将早期miRNA与蛋白质生物标志物相结合的模型,其预后性能优于蛋白质生物标志物模型。