NIHR Surgical Reconstruction and Microbiology Research Centre, Institute of Inflammation and Ageing, Birmingham University Medical School, Birmingham, B15 2TT UK.
NIHR Surgical Reconstruction and Microbiology Research Centre, Institute of Inflammation and Ageing, Birmingham University Medical School, Birmingham, B15 2TT UK ; Healing Foundation Centre for Burns Research, Queen Elizabeth Hospital, Birmingham, B15 2WB UK.
Burns Trauma. 2016 Sep 21;4:33. doi: 10.1186/s41038-016-0059-3. eCollection 2016.
As secondary complications remain a significant cause of morbidity and mortality amongst hospitalised trauma patients, the need to develop novel approaches by which to identify patients at risk of adverse outcome is becoming increasingly important. Centred on the idea that patients who experience "poor" outcome post trauma elicit a response to injury that is distinct from those who experience "good" outcome, tailored therapeutics is an emerging concept aimed at improving current treatment regimens by promoting patient-specific therapies. Making use of recent advancements in the fields of genomics, proteomics and metabolomics, numerous groups have undertaken a systems-based approach to analysing the acute immune and inflammatory response to major traumatic and thermal injury in an attempt to uncover a single or combination of biomarkers that can identify patients at risk of adverse outcome. Early results are encouraging, with all three approaches capable of discriminating patients with "good" outcome from those who develop nosocomial infections, sepsis and multiple organ failure, with differences apparent in blood samples acquired as early as 2 h post injury. In particular, genomic data is proving to be highly informative, identifying patients at risk of "poor" outcome with a higher degree of sensitivity and specificity than statistical models built upon data obtained from existing anatomical and physiological scoring systems. Here, focussing predominantly upon human-based research, we provide an overview of the findings of studies that have investigated the immune and inflammatory response to major traumatic and thermal injury at the genomic, protein and metabolite level, and consider both the diagnostic and prognostic potential of these approaches.
由于继发性并发症仍然是住院创伤患者发病率和死亡率的一个重要原因,因此开发新的方法来识别有不良预后风险的患者变得越来越重要。基于这样一种观点,即经历“不良”创伤后结果的患者会引起与经历“良好”创伤后结果的患者不同的反应,针对特定患者的治疗是一种新兴的概念,旨在通过促进针对特定患者的治疗来改善当前的治疗方案。利用基因组学、蛋白质组学和代谢组学领域的最新进展,许多研究小组采用了基于系统的方法来分析严重创伤和热损伤后的急性免疫和炎症反应,试图发现一种或多种能够识别有不良预后风险的患者的生物标志物。早期结果令人鼓舞,所有三种方法都能够区分具有“良好”预后的患者和发生医院感染、败血症和多器官衰竭的患者,在受伤后 2 小时即可从血液样本中观察到差异。特别是,基因组数据被证明具有高度的信息性,能够识别出有“不良”预后风险的患者,其敏感性和特异性均高于基于现有解剖学和生理学评分系统获得的数据构建的统计模型。在这里,我们主要关注基于人类的研究,概述了研究人员在基因组、蛋白质和代谢物水平上对严重创伤和热损伤后的免疫和炎症反应进行的研究结果,并考虑了这些方法的诊断和预后潜力。