Ludwig Katelyn R, Hummon Amanda B
Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN, USA.
Mol Biosyst. 2017 Mar 28;13(4):648-664. doi: 10.1039/c6mb00656f.
Sepsis is a serious medical condition that occurs in 30% of patients in intensive care units (ICUs). Early detection of sepsis is key to prevent its progression to severe sepsis and septic shock, which can cause organ failure and death. Diagnostic criteria for sepsis are nonspecific and hinder a timely diagnosis in patients. Therefore, there is currently a large effort to detect biomarkers that can aid physicians in the diagnosis and prognosis of sepsis. Mass spectrometry is often the method of choice to detect metabolomic and proteomic changes that occur during sepsis progression. These "omics" strategies allow for untargeted profiling of thousands of metabolites and proteins from human biological samples obtained from septic patients. Differential expression of or modifications to these metabolites and proteins can provide a more reliable source of diagnostic biomarkers for sepsis. Here, we focus on the current knowledge of biomarkers of sepsis and discuss the various mass spectrometric technologies used in their detection. We consider studies of the metabolome and proteome and summarize information regarding potential biomarkers in both general and neonatal sepsis.
脓毒症是一种严重的病症,在重症监护病房(ICU)的患者中发生率为30%。早期发现脓毒症是预防其进展为严重脓毒症和脓毒性休克的关键,严重脓毒症和脓毒性休克可导致器官衰竭和死亡。脓毒症的诊断标准不具有特异性,会妨碍对患者的及时诊断。因此,目前人们正在大力寻找能够帮助医生进行脓毒症诊断和预后评估的生物标志物。质谱分析通常是检测脓毒症进展过程中发生代谢组和蛋白质组变化的首选方法。这些“组学”策略能够对来自脓毒症患者的人体生物样本中的数千种代谢物和蛋白质进行非靶向分析。这些代谢物和蛋白质的差异表达或修饰可为脓毒症诊断生物标志物提供更可靠的来源。在此,我们聚焦于脓毒症生物标志物的现有知识,并讨论用于检测这些生物标志物的各种质谱技术。我们考量了代谢组和蛋白质组的研究,并总结了有关一般脓毒症和新生儿脓毒症潜在生物标志物的信息。