Todd S Rob, Kao Lillian S, Catania Anna, Mercer David W, Adams Sasha D, Moore Frederick A
Department of Surgery, Weill Medical College of Cornell University, Houston, Texas 77030, USA.
J Trauma. 2009 Feb;66(2):465-9. doi: 10.1097/TA.0b013e31818b1e04.
Alpha-melanocyte stimulating hormone (alpha-MSH) is a neuropeptide which modulates inflammation. Prior studies have documented decreased alpha-MSH concentrations in patients with acute traumatic brain injury and subarachnoid hemorrhage. We hypothesized that alpha-MSH levels would be decreased in critically injured patients and that this would correlate with poor outcome.
We performed a retrospective review of prospectively collected data more than 12 months ending December 2005. alpha-MSH concentrations were measured in major torso trauma patients (excluding severe head injuries) who underwent standardized shock resuscitation. alpha-MSH concentrations were measured every 4 hours for the first 24 hours of intensive care unit admission and daily thereafter for hospital days 2 to 5. Controls were similarly aged, healthy volunteers. Outcomes measured included lengths of stay, infectious morbidity, and the incidence of multiple organ failure (MOF) and mortality.
Fifty-one trauma patients were studied with a median age of 33 (22-54) years. Seventy-five percent were male and 82% sustained blunt trauma. The median Injury Severity Score was 25 (16-34). Eighteen percent of the patients developed MOF, 18% died, and 24% developed MOF and died. The mean initial (first value on the first day) alpha-MSH concentration was significantly lower than in controls (15.9 pg/mL +/- 7.6 pg/mL vs. 26.1 pg/mL +/- 7.4 pg/mL, p = 0.0008) and did not change significantly during the 5-day study period. On univariate and adjusted multivariate analyses, initial alpha-MSH concentrations did not predict either MOF or mortality.
The current study is the first to document significantly decreased alpha-MSH concentrations in critically injured trauma patients as compared with controls. Furthermore, alpha-MSH concentrations remained so throughout the study period.
α-黑素细胞刺激素(α-MSH)是一种调节炎症的神经肽。先前的研究已证明急性创伤性脑损伤和蛛网膜下腔出血患者的α-MSH浓度降低。我们假设严重受伤患者的α-MSH水平会降低,且这与不良预后相关。
我们对截至2005年12月的12个月以上前瞻性收集的数据进行了回顾性分析。对接受标准化休克复苏的主要躯干创伤患者(不包括严重头部损伤)测量α-MSH浓度。在重症监护病房入院的头24小时内每4小时测量一次α-MSH浓度,此后在住院第2至5天每天测量一次。对照组为年龄相仿的健康志愿者。测量的结果包括住院时间、感染发病率、多器官功能衰竭(MOF)发生率和死亡率。
研究了51例创伤患者,中位年龄为33(22 - 54)岁。75%为男性,82%为钝性创伤。中位损伤严重度评分为25(16 - 34)。18%的患者发生MOF,18%死亡,24%发生MOF并死亡。平均初始(第一天的第一个值)α-MSH浓度显著低于对照组(15.9 pg/mL±7.6 pg/mL对26.1 pg/mL±7.4 pg/mL,p = 0.0008),且在为期5天的研究期间无显著变化。在单变量和校正多变量分析中,初始α-MSH浓度均不能预测MOF或死亡率。
本研究首次证明与对照组相比,严重受伤的创伤患者的α-MSH浓度显著降低。此外,在整个研究期间α-MSH浓度一直如此。