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The value of circulating long non‐coding RNA maternally expressed gene 3 as a predictor of higher acute respiratory distress syndrome risk and 28‐day mortality in sepsis patients

机译:循环长期非编码RNA母体表达基因3的值作为急性呼吸困难综合征风险和脓毒症患者28天死亡率的预测因子

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Objective This study was to evaluate the potential of long non‐coding RNA maternally expressed gene 3 (lncRNA MEG3) in predicting acute respiratory distress syndrome (ARDS) risk and its correlation with prognosis in sepsis patients. Methods The plasma samples were obtained from 112 sepsis patients within 24?hours after admission and 100 healthy controls (HCs) at enrollment. The lncRNA MEG3 expression in plasma samples was determined by RT‐qPCR. In sepsis patients, ARDS occurrence was assessed based on Berlin definition of ARDS and 28‐day mortality risk was evaluated. Results LncRNA MEG3 expression was increased in sepsis patients compared with HCs. During 28‐day duration, 30 sepsis patients occurred ARDS and 82 sepsis patients did not occur ARDS. LncRNA MEG3 expression was elevated in ARDS sepsis patients compared with non‐ARDS sepsis patients, then the following receiver‐operating characteristic (ROC) curve analysis disclosed that lncRNA MEG3 predicted ARDS risk (area under the curve (AUC)?=?0.775), which was further validated as an independent risk factor by multivariate logistic regression. Furthermore, lncRNA MEG3 was positively correlated with chronic obstructive pulmonary disease, respiratory infection, acute physiology and chronic health evaluation II score, sequential organ failure assessment score, white blood cell, and C‐reactive protein, while negatively correlated with albumin in sepsis patients. Additionally, lncRNA MEG3 was elevated in 28‐day deaths compared with 28‐day survivors, and it predicted 28‐day mortality risk in sepsis patients (AUC?=?0.708) by ROC curve analysis. Conclusion LncRNA MEG3 might represent as a valuable biomarker for individualizing prevention strategies against ARDS and improving prognosis in sepsis.
机译:目的本研究是评估长期非编码RNA母体表达基因3(LNCRNA MEG3)的潜力在预测急性呼吸窘迫综合征(ARDS)风险及其与败血症患者预后的相关性。方法在入院后24小时内从112例脓毒症患者获得等离子体样品,并在注册时的100小时患者(HCS)。通过RT-QPCR测定血浆样品中的LNCRNA MEG3表达。在败血症患者中,基于ARDS的柏林定义和28天的死亡率进行评估ARDS发生。结果与HCS相比,败血症患者中LNCRNA MEG3表达增加。在28天的持续时间内,30例脓毒症患者发生ARDS和82例脓毒症患者没有发生ARDS。与非ARDS败血症患者相比,在ARDS Sepsis患者中升高了LNCRNA MEG3表达,然后以下接收器操作特征(ROC)曲线分析公开了LNCRNA MEG3预测的ARDS风险(曲线下的面积(AUC)?=?0.775),通过多变量逻辑回归进一步验证为独立的危险因素。此外,LNCRNA MEG3与慢性阻塞性肺疾病,呼吸道感染,急性生理学和慢性健康评估II评分,顺序器官衰竭评估评分,白细胞和C反应蛋白,同时与败血症患者中白蛋白与白蛋白相关的呈正相关。此外,与28天的幸存者相比,LNCRNA Meg3升高,患者升高,它通过ROC曲线分析预测了脓毒症患者的28天死亡率风险(AUC?= 0.708)。结论LNCRNA MEG3可能代表作为益智ARDS的预防策略和改善败血症预后的珍贵生物标志物。

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