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早产儿坏死性小肠结肠炎尿液代谢组学的初步病例对照研究。

A pilot case-control study of urine metabolomics in preterm neonates with necrotizing enterocolitis.

机构信息

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

School of Chemistry, Aristotle University of Thessaloniki, Greece.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jun 1;1117:10-21. doi: 10.1016/j.jchromb.2019.04.019. Epub 2019 Apr 8.

DOI:10.1016/j.jchromb.2019.04.019
PMID:30991202
Abstract

Necrotizing enterocolitis (NEC) is a leading cause of gastrointestinal morbidity and mortality in preterm neonates. The aim of this pilot study was to explore using metabolomics alternations in the urine metabolites related to NEC that could possibly serve as diagnostic biomarkers of the disease. Urine samples were prospectively collected at the day of initial evaluation for NEC from 15 diseased preterm neonates (five Bell's stage I and ten stage II/III) and an equal number of matched controls. Urine metabolic profiles were assessed using non-targeted nuclear magnetic resonance spectroscopy and targeted liquid chromatography-tandem mass spectrometry monitoring 108 metabolites. Multivariate statistical models with data from either analytical approach showed clear separation between the metabolic profiles of neonates with NEC and controls. Twenty-five discriminant metabolites were identified belonging to amino and organic acids, sugars and vitamins. A number of metabolite combinations were found to have an excellent diagnostic performance in detecting neonates developing NEC. Our results show that the metabolic profile of neonates with NEC differs significantly from that of controls, making possible their separation using urine metabolomic analysis. Nevertheless, whether the small set of significant metabolites detected in this investigation could be used as early diagnostic biomarkers of NEC should be validated in larger studies.

摘要

坏死性小肠结肠炎(NEC)是早产儿胃肠道发病率和死亡率的主要原因。本初步研究的目的是探讨与 NEC 相关的尿液代谢物中代谢组学改变是否可作为该疾病的诊断生物标志物。前瞻性地从 15 例患有 NEC 的早产儿(5 例 Bell Ⅰ期和 10 例Ⅱ/Ⅲ期)和相同数量的匹配对照组中,在最初评估的当天收集尿液样本。使用非靶向核磁共振波谱和靶向液相色谱-串联质谱监测 108 种代谢物评估尿液代谢谱。两种分析方法的数据得出的多变量统计模型显示,患有 NEC 的新生儿和对照组之间的代谢谱有明显的分离。确定了 25 种有判别能力的代谢物,属于氨基酸和有机酸、糖和维生素。发现一些代谢物组合在检测即将发生 NEC 的新生儿方面具有出色的诊断性能。我们的结果表明,患有 NEC 的新生儿的代谢谱与对照组有明显差异,因此可以通过尿液代谢组学分析进行分离。然而,本研究中检测到的少量显著代谢物是否可作为 NEC 的早期诊断生物标志物,应在更大的研究中进行验证。

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