Ou Hao, Xiao Xianzhong, Jiang Yu, Peng Yue, Yang Mingshi, Gao Min
Translational Medicine Center of Sepsis, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Department of Critical Care Medicine, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Exp Ther Med. 2018 Dec;16(6):4707-4711. doi: 10.3892/etm.2018.6759. Epub 2018 Sep 18.
The expression of microRNA-23b in peripheral blood leukocytes of patients with sepsis was investigated to assess the correlations with leukocyte, E-selectin, ICAM-1 and disease severity. The expression of microRNA-23b in peripheral blood leukocytes from 87 patients with sepsis, 50 patients with systemic inflammatory response syndrome (SIRS) and 50 normal controls were measured by reverse transcription-quantitative PCR (RT-qPCR), and stability of microRNA-23b was evaluated. Enzyme-linked immunosorbent assay (ELISA) was used to detect E-selectin and ICAM-1. Sequential organ failure assessment (SOFA) scoring system was used to assess the severity of sepsis patients. Correlation analysis was performed between microRNA-23b and the total number of white blood cells (WBC), E-selectin, ICAM-1, and SOFA scores. Compared with the normal control group, the expression level of microRNA-23b in the sepsis group was significantly decreased (P<0.05), and WBC and E-selectin were significantly increased (P<0.05). ICAM-1 level in the sepsis and the SIRS groups was significantly higher than that in the control group (P<0.05), and it is also higher in the sepsis group than in the SIRS group. In the sepsis group, the expression level of microRNA-23b in the death group was significantly lower than that in the survivor group (P<0.05), while the level of E-selectin, ICAM-1, and SOFA scores were significantly higher in the death group than in the survivor group (P<0.05), while there was no significant difference in WBC between the groups (P>0.05). The expression level of microRNA-23b in patients with sepsis was significantly negatively correlated with SOFA scores, E-selectin, and ICAM-1 (r=-0.633, -0.585, and -0.439, respectively, P<0.05). The expression of microRNA-23b in peripheral blood of patients with sepsis is related to the manifestation of the inflammatory state, and can be used to judge the severity and prognosis of patients with this disease.
研究脓毒症患者外周血白细胞中微小RNA-23b的表达,以评估其与白细胞、E选择素、细胞间黏附分子-1(ICAM-1)及疾病严重程度的相关性。采用逆转录定量聚合酶链反应(RT-qPCR)检测87例脓毒症患者、50例全身炎症反应综合征(SIRS)患者及50例正常对照者外周血白细胞中微小RNA-23b的表达,并评估微小RNA-23b的稳定性。采用酶联免疫吸附测定(ELISA)法检测E选择素和ICAM-1。采用序贯器官衰竭评估(SOFA)评分系统评估脓毒症患者的严重程度。对微小RNA-23b与白细胞总数(WBC)、E选择素、ICAM-1及SOFA评分进行相关性分析。与正常对照组相比,脓毒症组微小RNA-23b表达水平显著降低(P<0.05),WBC及E选择素显著升高(P<0.05)。脓毒症组和SIRS组ICAM-1水平显著高于对照组(P<0.05),且脓毒症组高于SIRS组。脓毒症组中,死亡组微小RNA-23b表达水平显著低于存活组(P<0.05),而死亡组E选择素、ICAM-1水平及SOFA评分显著高于存活组(P<0.05),但两组间WBC差异无统计学意义(P>0.05)。脓毒症患者微小RNA-23b表达水平与SOFA评分、E选择素及ICAM-1显著负相关(r分别为-0.633、-0.585和-0.439,P<0.05)。脓毒症患者外周血中微小RNA-23b的表达与炎症状态表现相关,可用于判断该疾病患者的严重程度及预后。