Han Yan, Li Yong, Jiang Ying
Clin Lab. 2016 Dec 1;62(12):2355-2360. doi: 10.7754/Clin.Lab.2016.160511.
Sepsis induced acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are lifethreatening disorders. Acute Physiology and Chronic Health Evaluation (APACHE) scores and several plasma biological markers have been identified to predict the death or treatment outcome of sepsis induced ALI. Immune related microRNAs also have the potential as biomarkers to monitor this kind of disease.
A total of 44 patients with severe sepsis, 102 patients with sepsis, and 19 healthy volunteers were enrolled in this study. Plasma miR-155 and miR-146a were determined by qRT-PCR. Genotyping analysis of miR146a rs2690164 was performed using PCR-restriction fragment length polymorphism assay.
The relative plasma miR-155 and miR-146a concentrations were significantly increased in severe sepsis and sepsis-induced cases of ALI, compared with control subjects. The AUC of miR-155 and miR-146a for predicting 30-day mortality in ALI patients was 0.782 (95% CI 0.694 - 0.870) and 0.733 (95% CI 0.640 - 0.827), respectively. CC genotype of miR-146a rs2910164 was associated with worse treatment outcome of these patients.
The current study provides evidence that the plasma miR-155 and miR-146a could be novel biomarkers for predicting the mortality and treatment outcome of sever sepsis and sepsis-induced acute lung injury.
脓毒症诱发的急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是危及生命的病症。急性生理与慢性健康状况评估(APACHE)评分及多种血浆生物标志物已被确定可预测脓毒症诱发ALI的死亡或治疗结果。免疫相关的微小RNA也有潜力作为监测此类疾病的生物标志物。
本研究共纳入44例严重脓毒症患者、102例脓毒症患者及19名健康志愿者。采用qRT-PCR测定血浆miR-155和miR-146a。使用PCR-限制性片段长度多态性分析对miR-146a rs2690164进行基因分型分析。
与对照组相比,严重脓毒症及脓毒症诱发ALI患者的血浆miR-155和miR-146a相对浓度显著升高。miR-155和miR-146a预测ALI患者30天死亡率的AUC分别为0.782(95%CI 0.694 - 0.870)和0.733(95%CI 0.640 - 0.827)。miR-146a rs2910164的CC基因型与这些患者较差的治疗结果相关。
本研究提供了证据表明血浆miR-155和miR-146a可能是预测严重脓毒症及脓毒症诱发急性肺损伤死亡率和治疗结果的新型生物标志物。