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早产儿发病前严重坏死性小肠结肠炎的粪便胺代谢产物分析:一项前瞻性病例对照研究。

Fecal amine metabolite analysis before onset of severe necrotizing enterocolitis in preterm infants: a prospective case-control study.

机构信息

Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands.

Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Sci Rep. 2022 Jul 19;12(1):12310. doi: 10.1038/s41598-022-16351-8.

Abstract

Infants developing necrotizing enterocolitis (NEC) have a different metabolomic profile compared to controls. The potential of specific metabolomics, i.e. amino acids and amino alcohols (AAA), as early diagnostic biomarkers for NEC is largely unexplored. In this multicenter prospective case-control study, longitudinally collected fecal samples from preterm infants (born <30 weeks of gestation) from 1-3 days before diagnosis of severe NEC (Bell's stage IIIA/IIIB), were analyzed by targeted high-performance liquid chromatography (HPLC). Control samples were collected from gestational and postnatal age-matched infants. Thirty-one NEC cases (15 NEC IIIA;16 NEC IIIB) with 1:1 matched controls were included. Preclinical samples of infants with NEC were characterized by five increased essential amino acids-isoleucine, leucine, methionine, phenylalanine and valine. Lysine and ethanolamine ratios were lower prior to NEC, compared to control samples. A multivariate model was rendered based on isoleucine, lysine, ethanolamine, tryptophan and ornithine, modestly discriminating cases from controls (AUC 0.67; p < 0.001). Targeted HPLC pointed to several specific AAA alterations in samples collected 1-3 days before NEC onset, compared to controls. Whether this reflects metabolic alterations and has a role in early biomarker development for NEC, has yet to be elucidated.

摘要

与对照相比,发生坏死性小肠结肠炎 (NEC) 的婴儿具有不同的代谢组学特征。特定代谢组学(即氨基酸和氨基醇 (AAA))作为 NEC 早期诊断生物标志物的潜力在很大程度上尚未得到探索。在这项多中心前瞻性病例对照研究中,对 1-3 天前诊断为严重 NEC(Bell 分期 IIIA/IIIB)的早产儿(<30 周胎龄)的纵向收集粪便样本进行了分析,采用靶向高效液相色谱法 (HPLC)。对照样本取自胎龄和出生后年龄匹配的婴儿。共纳入 31 例 NEC 病例(15 例 NEC IIIA;16 例 NEC IIIB),与 1:1 匹配的对照。与对照样本相比,NEC 患儿的临床前样本特征为五种必需氨基酸增加,即异亮氨酸、亮氨酸、蛋氨酸、苯丙氨酸和缬氨酸。在发生 NEC 之前,赖氨酸和乙醇胺的比值较低,与对照样本相比。根据异亮氨酸、赖氨酸、乙醇胺、色氨酸和鸟氨酸构建了一个多变量模型,适度地区分了病例和对照(AUC 0.67;p<0.001)。与对照相比,在 NEC 发作前 1-3 天采集的样本中,靶向 HPLC 指出了几种特定的 AAA 改变。这是否反映了代谢改变,以及在 NEC 的早期生物标志物开发中是否具有作用,还有待阐明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03a2/9296556/ca2535711670/41598_2022_16351_Fig1_HTML.jpg

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