Department of Trauma Surgery, University Hospital Munich, Ludwig-Maximilians-University, Munich, Germany.
Division of Respiratory Medicine and Thoracic Oncology, Department of Internal Medicine V, University of Munich (LMU), Munich, Germany.
Shock. 2020 Jan;53(1):63-70. doi: 10.1097/SHK.0000000000001344.
A declining selenium (Se) status constitutes a characteristic of critical illness and may affect disease course and survival. The dynamics of trauma-induced changes in biomarkers of Se status are poorly characterized, and an association with multiple organ failure (MOF) and mortality can be hypothesized. It was the aim of this study to investigate Se and selenoprotein P (SELENOP) concentrations in major trauma patients during the early posttraumatic period.
Twenty-four patients after major trauma (ISS ≥16) were included at our level one trauma center. Se supplementation ever during the 90-day observation period was defined as an exclusion criterion. Serum samples were drawn within less than 60 min after trauma, and after 6 h, 12 h, 24 h, 48 h, and 72 h. Serum Se was analyzed by X-ray fluorescence and SELENOP concentrations by ELISA. The data were correlated to clinical parameters, occurrence of MOF defined by MOF and APACHE II score, lung injury defined by Horowitz index and clinical outcome (90-days survival).
Serum Se and SELENOP concentrations of the trauma patients were significantly below the average of healthy European subjects (mean ±SD; Se, 41.2±8.1 vs. 84.7±23.3 μg/L, P < 0.001; SePP, 1.5±0.3 vs. 4.3±1.0 mg/L, P < 0.001). A strong deficit was present already at the first time point (Se; 33.6±10.5 μg/L, SELENOP: 1.4±0.5 mg/L). The clinical scores collectively showed an inverse relation between health status and Se biomarkers. Patients who did not survive the 90-day observation period exhibited significantly lower initial post-trauma Se status than the surviving patients (mean±SD; Se, 24.7±7.2 vs. 39.2±8.4 μg/L, P<0.05; SePP, 1.1±0.4 vs. 1.6±0.4 mg/L, P<0.05).
Very low Se and SELENOP concentrations occur fast after major trauma and are associated with poor survival odds. These findings support the notion that early Se substitution may constitute a meaningful adjuvant treatment strategy in trauma patients.
硒(Se)状态下降是危重病的特征之一,可能影响疾病进程和生存。创伤后生物标志物硒状态变化的动态特征描述不足,并且可以假设其与多器官衰竭(MOF)和死亡率相关。本研究旨在调查严重创伤患者创伤后早期的 Se 和硒蛋白 P(SELENOP)浓度。
在我们的一级创伤中心纳入了 24 名严重创伤患者(ISS≥16)。在 90 天观察期内接受过 Se 补充治疗的患者被排除在外。创伤后不到 60 分钟内抽取血清样本,然后在 6、12、24、48 和 72 小时抽取。采用 X 射线荧光法分析血清 Se,采用 ELISA 法分析 SELENOP 浓度。将数据与临床参数、MOF 的发生(MOF 和 APACHE II 评分)、肺损伤(Horowitz 指数)和临床结局(90 天生存率)相关联。
创伤患者的血清 Se 和 SELENOP 浓度明显低于欧洲健康人群的平均水平(平均值±标准差;Se,41.2±8.1 vs. 84.7±23.3μg/L,P<0.001;SELENOP,1.5±0.3 vs. 4.3±1.0mg/L,P<0.001)。首次检测时就出现了严重不足(Se,33.6±10.5μg/L;SELENOP,1.4±0.5mg/L)。临床评分总体上显示健康状况与 Se 生物标志物呈负相关。在 90 天观察期内未存活的患者与存活的患者相比,初始创伤后 Se 状态明显更低(平均值±标准差;Se,24.7±7.2 vs. 39.2±8.4μg/L,P<0.05;SELENOP,1.1±0.4 vs. 1.6±0.4mg/L,P<0.05)。
严重创伤后 Se 和 SELENOP 浓度迅速下降,与生存几率较差相关。这些发现支持早期 Se 替代可能是创伤患者有意义的辅助治疗策略的观点。