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早期血浆单核细胞趋化蛋白-1可预测创伤患者脓毒症的发生:一项前瞻性观察研究。

Early plasma monocyte chemoattractant protein 1 predicts the development of sepsis in trauma patients: A prospective observational study.

作者信息

Wang Yuchang, Liu Qinxin, Liu Tao, Zheng Qiang, Xu Xi'e, Liu Xinghua, Gao Wei, Li Zhanfei, Bai Xiangjun

机构信息

Department of Traumatic Surgery, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.

出版信息

Medicine (Baltimore). 2018 Apr;97(14):e0356. doi: 10.1097/MD.0000000000010356.

Abstract

Monocyte chemoattractant protein 1 (MCP-1) is an initiating cytokine of the inflammatory cascade. Extracellular MCP-1 exhibits pro-inflammatory characteristic and plays a central pathogenic role in critical illness. The purpose of the study was to identify the association between plasma MCP-1 levels and the development of sepsis after severe trauma.The plasma levels of MCP-1 in severe trauma patients were measured by a quantitative enzyme-linked immune sorbent assay and the dynamic release patterns were recorded at three time points during seven days post-trauma. The related factors of prognosis were compared between sepsis and non-sepsis groups and analyzed using multivariate logistic regression analysis. We also used receiver operating characteristic (ROC) curves to assess the values of different variables in predicting sepsis.A total of 72 patients who met criteria indicative of severe trauma (72.22% of male; mean age, 49.40 ± 14.29 years) were enrolled. Plasma MCP-1 concentrations significantly increased on post-trauma day 1 and that this increase was significantly correlated with the Injury Severity Score (ISS) and interleukin-6 (IL-6). Multivariate logistic regression analysis showed that early MCP-1, ISS, and IL-6 were independent risk factors for sepsis in severe trauma patients. Incorporation of the early MCP-1 into the ISS can increase the discriminative performance for predicting development of sepsis.Early plasma MCP-1 concentrations can be used to assess the severity of trauma and is correlated with the development of sepsis after severe trauma. The addition of the early MCP-1 levels to the ISS significantly improves its ability to predict development of sepsis.

摘要

单核细胞趋化蛋白1(MCP-1)是炎症级联反应的起始细胞因子。细胞外MCP-1具有促炎特性,在危重病中起核心致病作用。本研究的目的是确定血浆MCP-1水平与严重创伤后脓毒症发生之间的关联。通过定量酶联免疫吸附测定法测量严重创伤患者血浆中MCP-1的水平,并记录创伤后7天内三个时间点的动态释放模式。比较脓毒症组和非脓毒症组的预后相关因素,并使用多因素逻辑回归分析进行分析。我们还使用受试者工作特征(ROC)曲线评估不同变量在预测脓毒症中的价值。

共纳入72例符合严重创伤标准的患者(男性占72.22%;平均年龄49.40±14.29岁)。创伤后第1天血浆MCP-1浓度显著升高,且这种升高与损伤严重程度评分(ISS)和白细胞介素-6(IL-6)显著相关。多因素逻辑回归分析表明,早期MCP-1、ISS和IL-6是严重创伤患者发生脓毒症的独立危险因素。将早期MCP-1纳入ISS可提高预测脓毒症发生的判别性能。

早期血浆MCP-1浓度可用于评估创伤严重程度,且与严重创伤后脓毒症的发生相关。将早期MCP-1水平加入ISS可显著提高其预测脓毒症发生的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/997d/5902265/0a5c6ccc141a/medi-97-e0356-g002.jpg

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