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新生儿晚发型败血症的病例对照研究中的尿代谢组学。

Urine metabolomics in neonates with late-onset sepsis in a case-control study.

机构信息

1st Department of Neonatology, School of Medicine, Aristotle University of Thessaloniki, Greece.

School of Chemistry, Aristotle University of Thessaloniki, Greece.

出版信息

Sci Rep. 2017 Apr 4;7:45506. doi: 10.1038/srep45506.

Abstract

Although late-onset sepsis (LOS) is a major cause of neonatal morbidity and mortality, biomarkers evaluated in LOS lack high diagnostic accuracy. In this prospective, case-control, pilot study, we aimed to determine the metabolic profile of neonates with LOS. Urine samples were collected at the day of initial LOS evaluation, the 3 and 10 day, thereafter, from 16 septic neonates (9 confirmed and 7 possible LOS cases) and 16 non-septic ones (controls) at respective time points. Urine metabolic profiles were assessed using non-targeted nuclear magnetic resonance spectroscopy and targeted liquid chromatography-tandem mass spectrometry analysis. Multivariate statistical models with data from either analytical approach showed clear separation between the metabolic profiles of septic neonates (both possible and confirmed) and the controls. Metabolic changes appeared to be related to disease progression. Overall, neonates with confirmed or possible LOS exhibited comparable metabolic profiles indicating similar metabolic alternations upon the onset of clinical manifestations. This methodology therefore enabled the discrimination of neonates with LOS from non-septic individuals, providing potential for further research toward the discovery of LOS-related biomarkers.

摘要

虽然晚发性败血症(LOS)是导致新生儿发病率和死亡率的主要原因,但在 LOS 中评估的生物标志物缺乏高诊断准确性。在这项前瞻性病例对照的初步研究中,我们旨在确定 LOS 新生儿的代谢特征。在初始 LOS 评估当天、第 3 天和第 10 天,分别从 16 例败血症新生儿(9 例确诊和 7 例可能的 LOS 病例)和 16 例非败血症新生儿(对照组)中采集尿液样本。使用非靶向核磁共振波谱和靶向液相色谱-串联质谱分析评估尿液代谢特征。使用两种分析方法的数据进行的多变量统计模型显示,败血症新生儿(包括确诊和可能的 LOS 病例)与对照组之间的代谢谱明显分离。代谢变化似乎与疾病进展有关。总体而言,确诊或可能的 LOS 新生儿表现出相似的代谢特征,表明在临床表现出现时发生类似的代谢改变。因此,该方法能够将 LOS 新生儿与非败血症个体区分开来,为进一步研究 LOS 相关生物标志物提供了潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c90/5379623/6fe949b0dec3/srep45506-f1.jpg

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