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粪便挥发性代谢组学预测早产儿革兰氏阴性迟发性败血症:一项全国性病例对照研究。

Fecal Volatile Metabolomics Predict Gram-Negative Late-Onset Sepsis in Preterm Infants: A Nationwide Case-Control Study.

作者信息

Frerichs Nina M, El Manouni El Hassani Sofia, Deianova Nancy, van Weissenbruch Mirjam M, van Kaam Anton H, Vijlbrief Daniel C, van Goudoever Johannes B, Hulzebos Christian V, Kramer Boris W, d'Haens Esther J, Cossey Veerle, de Boode Willem P, de Jonge Wouter J, Wicaksono Alfian N, Covington James A, Benninga Marc A, de Boer Nanne K H, Niemarkt Hendrik J, de Meij Tim G J

机构信息

Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.

Department of Neonatology, Amsterdam Reproduction and Development Research Institute, Emma Children's Hospital, 1105 AZ Amsterdam, The Netherlands.

出版信息

Microorganisms. 2023 Feb 24;11(3):572. doi: 10.3390/microorganisms11030572.

Abstract

Early detection of late-onset sepsis (LOS) in preterm infants is crucial since timely treatment initiation is a key prognostic factor. We hypothesized that fecal volatile organic compounds (VOCs), reflecting microbiota composition and function, could serve as a non-invasive biomarker for preclinical pathogen-specific LOS detection. Fecal samples and clinical data of all preterm infants (≤30 weeks' gestation) admitted at nine neonatal intensive care units in the Netherlands and Belgium were collected daily. Samples from one to three days before LOS onset were analyzed by gas chromatography-ion mobility spectrometry (GC-IMS), a technique based on pattern recognition, and gas chromatography-time of flight-mass spectrometry (GC-TOF-MS), to identify unique metabolites. Fecal VOC profiles and metabolites from infants with LOS were compared with matched controls. Samples from 121 LOS infants and 121 matched controls were analyzed using GC-IMS, and from 34 LOS infants and 34 matched controls using GC-TOF-MS. Differences in fecal VOCs were most profound one and two days preceding LOS (Area Under Curve; -value: 0.73; = 0.02, 0.83; < 0.002, respectively) and two and three days before gram-negative LOS (0.81; < 0.001, 0.85; < 0.001, respectively). GC-TOF-MS identified pathogen-specific discriminative metabolites for LOS. This study underlines the potential for VOCs as a non-invasive preclinical diagnostic LOS biomarker.

摘要

早产婴儿晚发性败血症(LOS)的早期检测至关重要,因为及时开始治疗是关键的预后因素。我们假设,反映微生物群组成和功能的粪便挥发性有机化合物(VOCs)可作为临床前病原体特异性LOS检测的非侵入性生物标志物。每天收集荷兰和比利时九个新生儿重症监护病房收治的所有早产婴儿(孕周≤30周)的粪便样本和临床数据。在LOS发作前1至3天的样本通过气相色谱-离子迁移谱(GC-IMS,一种基于模式识别的技术)和气相色谱-飞行时间质谱(GC-TOF-MS)进行分析,以识别独特的代谢物。将LOS婴儿的粪便VOC谱和代谢物与匹配的对照组进行比较。使用GC-IMS分析了121名LOS婴儿和121名匹配对照组的样本,使用GC-TOF-MS分析了34名LOS婴儿和34名匹配对照组的样本。粪便VOCs的差异在LOS前1天和2天最为显著(曲线下面积;P值:分别为0.73;P = 0.02,0.83;P < 0.002),在革兰氏阴性LOS前2天和3天也最为显著(分别为0.81;P < 0.001,0.85;P < 0.001)。GC-TOF-MS确定了LOS的病原体特异性鉴别代谢物。本研究强调了VOCs作为LOS非侵入性临床前诊断生物标志物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e193/10054547/4ec15da87966/microorganisms-11-00572-g001.jpg

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