Hao Jinxiang, Xu Junxu, Liang Yong, Chen Yu, Wu Tingshi, Xiao Chengqin
Department of Respiratory, the Third People's Hospital of Haikou, Haikou 571100, Hainan, China. Corresponding author: Hao Jinxiang, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2019 Jun;31(6):694-698. doi: 10.3760/cma.j.issn.2095-4352.2019.06.007.
To investigate the prognostic value of microRNA-122 (miR-122) combined with acute physiology and chronic health evaluation II (APACHE II) score in patient with acute respiratory distress syndrome (ARDS), and to provide evidence for the diagnosis and treatment of ARDS.
ARDS patients admitted to the Third People's Hospital of Haikou City from January 2016 to December 2018 were enrolled. The general data, serum miR-122 expression level and APACHE II score within 24 hours were collected. The patients were divided into survival group and death group according to the survival status of ARDS patients. ARDS patients were divided into low-risk group (< 10 scores), medium-risk group (10-20 scores) and high-risk group (> 20 scores) according to APACHE II score. Predictive values of miR-122 and APACHE II scores on prognosis in ARDS patients were evaluated by the receiver operating characteristic (ROC) curve. The correlation between the serum miR-122 expression and APACHE II score in patients with ARDS was calculated by Pearson correlation analysis.
A total of 142 ARDS patients were selected, 94 male and 48 female; with age (56.80±11.30) years old; 55 deaths and 87 survivors; 67 of high-risk, 48 of medium-risk and 27 of low-risk. The expression of serum miR-122 and APACHE II score in the death group were significantly higher than those in the survival group [miR-122 (2): 0.26±0.12 vs. 0.07±0.03, APACHE II: 31.84±4.25 vs. 15.30±2.60, both P < 0.01]. With the severity increase of the disease, the serum miR-122 expression level, APACHE II score, and mortality rate of ARDS patients gradually elevated, and the difference between the two groups was significant in the low-risk group, medium-risk group, and high-risk group [miR-122 (2): 0.05±0.02, 0.14±0.06, 0.23±0.09; APACHE II: 12.30±2.15, 20.62±3.40, 28.90±3.60; mortality rate: 11.1%, 31.2%, 55.2%, respectively, all P < 0.05]. ROC curve analysis showed that miR-122 and APACHE II score could predict the death of ARDS patients, and the area under the ROC curve (AUC) was 0.835 [95% confidence interval (95%CI) = 0.776-0.893] and 0.790 (95%CI = 0.732-0.854); the predicted value of the miR-122 combined with APACHE II score (AUC = 0.918, 95%CI = 0.857-0.972) was higher than the single miR-122 and APACHE II score (both P < 0.05), with sensitivity and specificity were 91.3% and 86.4% respectively. The correlation analysis showed that the expression of serum miR-122 was positively correlated with APACHE II score in death patient with ARDS (r = 0.825, P < 0.01).
Elevated serum miR-122 expression level is associated with disease severity and prognosis of ARDS patients; miR-122 combination with APACHE II score has a high evaluation value on prognosis of ARDS patients.
探讨微小RNA-122(miR-122)联合急性生理与慢性健康状况评分系统II(APACHE II)对急性呼吸窘迫综合征(ARDS)患者预后的评估价值,为ARDS的诊治提供依据。
选取2016年1月至2018年12月在海口市第三人民医院收治的ARDS患者。收集患者的一般资料、血清miR-122表达水平及入院24小时内的APACHE II评分。根据ARDS患者的生存情况分为生存组和死亡组。根据APACHE II评分将ARDS患者分为低危组(<10分)、中危组(10 - 20分)和高危组(>20分)。采用受试者工作特征(ROC)曲线评估miR-122和APACHE II评分对ARDS患者预后的预测价值。采用Pearson相关分析计算ARDS患者血清miR-122表达与APACHE II评分的相关性。
共纳入142例ARDS患者,男94例,女48例;年龄(56.80±ll.30)岁;死亡55例,存活87例;高危组67例,中危组48例,低危组27例。死亡组血清miR-122表达及APACHE II评分均显著高于生存组[miR-122(2):0.26±0.12比0.07±0.03,APACHE II:31.84±4.25比15.30±2.60,均P<0.01]。随着疾病严重程度增加,ARDS患者血清miR-122表达水平、APACHE II评分及死亡率逐渐升高,低危组、中危组和高危组两组间差异均有统计学意义[miR-122(2):0.05±0.02、0.14±0.06、0.23±0.09;APACHE II:12.30±2.15、20.62±3.40、28.90±3.60;死亡率分别为11.1%、31.2%、55.2%,均P<0.05]。ROC曲线分析显示,miR-122和APACHE II评分均可预测ARDS患者死亡,ROC曲线下面积(AUC)分别为0.835[95%置信区间(95%CI)=0.776 - 0.893]和0.790(95%CI = 0.732 - 0.854);miR-122联合APACHE II评分(AUC = 0.918,95%CI = 0.857 - 0.972)预测价值高于单一miR-122和APACHE II评分(均P<0.05),敏感度和特异度分别为91.3%和86.4%。相关分析显示,ARDS死亡患者血清miR-122表达与APACHE II评分呈正相关(r = 0.825,P<0.()1)。
血清miR-122表达水平升高与ARDS患者疾病严重程度及预后相关;miR-122联合APACHE II评分对ARDS患者预后有较高评估价值。