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MicroRNA‐146b correlates with decreased acute respiratory distress syndrome risk, reduced disease severity, and lower 28‐day mortality in sepsis patients

机译:microRNA-146B与急性呼吸困难综合征风险,降低疾病严重程度和脓毒症患者的较低死亡率降低相关

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Objective This study aimed to investigate the predictive value of microRNA‐146b (miR‐146b) on acute respiratory distress syndrome (ARDS) risk, and the correlation of miR‐146b with disease severity and 28‐day mortality in sepsis patients. Methods A total of 104 sepsis patients and 100 healthy controls (HCs) were consecutively enrolled, and miR‐146b relative expression in their plasma samples was detected by reverse transcription‐quantitative polymerase chain reaction. In sepsis patients, disease severity was assessed using Acute Physiology and Chronic Health Evaluation II (APACHE II) score and Sequential Organ Failure Assessment (SOFA) score. ARDS occurrence and 28‐day mortality were recorded. Results MiR‐146b was decreased in sepsis patients compared to HCs. ARDS occurred in 30 (28.8%) sepsis patients, and miR‐146b was reduced in ARDS sepsis patients compared to non‐ARDS sepsis patients. Meanwhile, miR‐146b distinguished ARDS sepsis patients from non‐ARDS sepsis patients (area under the curve (AUC): 0.728, 95% confidence interval (CI): 0.627‐0.829). Subsequent multivariate logistic regression showed that miR‐146b, age, smoke, respiratory infection, and serum creatinine predicted ARDS risk independently, and their combination well‐discriminated ARDS sepsis patients from non‐ARDS sepsis patients (AUC: 0.863, 95% CI: 0.792‐0.934). Additionally, miR‐146b was negatively correlated with serum creatinine, white blood cell, C‐reactive protein, APACHE II score, and SOFA score, while positively correlated with albumin. Regarding prognosis, miR‐146b was decreased in 28‐day sepsis deaths compared to 28‐day sepsis survivors, and it discriminated 28‐day sepsis deaths from 28‐day sepsis survivors (AUC: 0.785, 95% CI: 0.680‐0.890). Conclusion MiR‐146b might serve as a potential biomarker for ARDS prevention and prognostic reflection in sepsis.
机译:目的本研究旨在探讨MicroRNA-146B(miR-146b)对急性呼吸窘迫综合征(ARDS)风险的预测值,以及MiR-146B在脓毒症患者中疾病严重程度和28天死亡率的相关性。方法通过逆转录定量聚合酶链反应,共纳入总共104名脓血病患者和100名健康对照(HCS),并检测其等离子体样品中的相对表达。在败血症患者中,使用急性生理学和慢性健康评估II(Apache II)评分和顺序器官失败评估(沙发)得分评估疾病严重程度。记录了ARDS发生和28天的死亡率。结果与HCS相比,败血症患者MIR-146B减少。 ARDS发生在30名(28.8%)败血症患者中,与非ARDS败血症患者相比,ARDS脓毒症患者的MIR-146B减少。同时,MIR-146B尊称来自非ARDS脓毒症患者的ARDS SEPSIS患者(曲线下的面积(AUC):0.728,95%置信区间(CI):0.627-0.829)。随后的多变量逻辑回归显示,MIR-146B,年龄,烟雾,呼吸道感染和血清肌酐独立预测ARA风险,其组合来自非ARDS SEPSIS患者(AUC:0.863,95%CI:0.792 -0.934)。另外,miR-146b与血清肌酐,白细胞,c反应蛋白,apacheII得分和沙发评分负相关,而与白蛋白呈正相关。关于预后,与28天的败血症幸存者相比,28天的脓毒症死亡人员减少了MiR-146B,从28天的败血症幸存者(AUC:0.785,95%CI:0.680-0.890)歧视了28天的败血症死亡。结论MIR-146B可以作为脓毒症中ARDS预防和预后反射的潜在生物标志物。

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