• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Emerging Biomarkers for Prediction and Early Diagnosis of Necrotizing Enterocolitis in the Era of Metabolomics and Proteomics.代谢组学和蛋白质组学时代坏死性小肠结肠炎预测与早期诊断的新兴生物标志物
Front Pediatr. 2020 Dec 8;8:602255. doi: 10.3389/fped.2020.602255. eCollection 2020.
2
Metabolomics in necrotizing enterocolitis: the state of the art.代谢组学在坏死性小肠结肠炎中的研究进展。
Expert Rev Mol Diagn. 2016 Oct;16(10):1053-1058. doi: 10.1080/14737159.2016.1211933. Epub 2016 Jul 22.
3
Urinary I-FABP, L-FABP, TFF-3, and SAA Can Diagnose and Predict the Disease Course in Necrotizing Enterocolitis at the Early Stage of Disease.尿 I-FABP、L-FABP、TFF-3 和 SAA 可在疾病早期诊断和预测坏死性小肠结肠炎的病程。
J Immunol Res. 2020 Mar 3;2020:3074313. doi: 10.1155/2020/3074313. eCollection 2020.
4
Targeted LC-MS/MS for the evaluation of proteomics biomarkers in the blood of neonates with necrotizing enterocolitis and late-onset sepsis.靶向 LC-MS/MS 法评估坏死性小肠结肠炎和晚发性败血症新生儿血液中的蛋白质组学生物标志物。
Anal Bioanal Chem. 2018 Nov;410(27):7163-7175. doi: 10.1007/s00216-018-1320-3. Epub 2018 Aug 23.
5
A pilot case-control study of urine metabolomics in preterm neonates with necrotizing enterocolitis.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。
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.
6
Elevated levels of circulating cell-free DNA and neutrophil proteins are associated with neonatal sepsis and necrotizing enterocolitis in immature mice, pigs and infants.循环中游离DNA和中性粒细胞蛋白水平升高与未成熟小鼠、猪和婴儿的新生儿败血症及坏死性小肠结肠炎有关。
Innate Immun. 2017 Aug;23(6):524-536. doi: 10.1177/1753425917719995. Epub 2017 Jul 17.
7
[Analysis of clinical characteristics of necrotizing enterocolitis in term infants].[足月儿坏死性小肠结肠炎的临床特征分析]
Zhonghua Yi Xue Za Zhi. 2016 Jun 14;96(22):1766-72. doi: 10.3760/cma.j.issn.0376-2491.2016.22.012.
8
Translational Metabolomics of Head Injury: Exploring Dysfunctional Cerebral Metabolism with Ex Vivo NMR Spectroscopy-Based Metabolite Quantification头部损伤的转化代谢组学:基于体外核磁共振波谱的代谢物定量分析探索脑代谢功能障碍
9
Necrotizing enterocolitis: a clinical review on diagnostic biomarkers and the role of the intestinal microbiota.坏死性小肠结肠炎:诊断生物标志物及肠道微生物组作用的临床综述
Inflamm Bowel Dis. 2015 Feb;21(2):436-44. doi: 10.1097/MIB.0000000000000184.
10
Biomarkers of necrotizing enterocolitis: a review of literature.坏死性小肠结肠炎的生物标志物:文献综述
J Matern Fetal Neonatal Med. 2018 Nov;31(22):3051-3064. doi: 10.1080/14767058.2017.1361925. Epub 2017 Aug 9.

引用本文的文献

1
Integrated analysis of serum metabolomics and fecal microbiome in infants with necrotizing enterocolitis.坏死性小肠结肠炎患儿血清代谢组学与粪便微生物组的综合分析
Front Microbiol. 2025 Jun 5;16:1584041. doi: 10.3389/fmicb.2025.1584041. eCollection 2025.
2
The predictive value of maternal and neonatal inflammatory biomarkers for necrotizing enterocolitis.孕产妇和新生儿炎症生物标志物对坏死性小肠结肠炎的预测价值。
Eur J Pediatr. 2025 Apr 28;184(5):316. doi: 10.1007/s00431-025-06146-0.
3
Cell-based therapies in preclinical models of necrotizing enterocolitis: a systematic review and meta-analysis.坏死性小肠结肠炎临床前模型中的细胞疗法:系统评价与荟萃分析。
Stem Cells Transl Med. 2025 Feb 11;14(2). doi: 10.1093/stcltm/szae102.
4
Applications of Metabolomics and Lipidomics in the Neonatal Intensive Care Unit.代谢组学和脂质组学在新生儿重症监护病房的应用
Neoreviews. 2025 Feb 1;26(2):e100-e114. doi: 10.1542/neo.26-2-011.
5
Integrated Analysis of Gut Microbiota and Metabolites in a Rat Necrotizing Enterocolitis Model.大鼠坏死性小肠结肠炎模型中肠道微生物群与代谢物的综合分析
Turk J Gastroenterol. 2025 Jan 20;36(5):312-320. doi: 10.5152/tjg.2025.24451.
6
Digging deeper into necrotizing enterocolitis: bridging clinical, microbial, and molecular perspectives.深入探究坏死性小肠结肠炎:连接临床、微生物和分子层面的观点
Gut Microbes. 2025 Dec;17(1):2451071. doi: 10.1080/19490976.2025.2451071. Epub 2025 Jan 18.
7
Insight of Intestinal Fatty Acid Binding Protein as a Potential Biomarker in the Biology of Epithelial Damage of Gastrointestinal Membrane.肠道脂肪酸结合蛋白作为胃肠膜上皮损伤生物学中潜在生物标志物的见解
Curr Protein Pept Sci. 2025;26(5):321-333. doi: 10.2174/0113892037311290240930054913.
8
Necrotizing Enterocolitis Detection in Premature Infants Using Broadband Optical Spectroscopy.利用宽带光学光谱法检测早产儿坏死性小肠结肠炎
J Biophotonics. 2025 Jan;18(1):e202400273. doi: 10.1002/jbio.202400273. Epub 2024 Nov 11.
9
Metabolomic analysis to predict the onset and severity of necrotizing enterocolitis.代谢组学分析预测坏死性小肠结肠炎的发病和严重程度。
BMC Gastroenterol. 2024 Oct 26;24(1):380. doi: 10.1186/s12876-024-03453-y.
10
Struggling to Understand the NEC Spectrum-Could the Integration of Metabolomics, Clinical-Laboratory Data, and Other Emerging Technologies Help Diagnosis?难以理解坏死性小肠结肠炎的谱系——代谢组学、临床实验室数据及其他新兴技术的整合能否有助于诊断?
Metabolites. 2024 Sep 26;14(10):521. doi: 10.3390/metabo14100521.

本文引用的文献

1
Increased Expression of microRNA-141-3p Improves Necrotizing Enterocolitis of Neonates Through Targeting MNX1.微小RNA-141-3p表达增加通过靶向MNX1改善新生儿坏死性小肠结肠炎。
Front Pediatr. 2020 Jul 28;8:385. doi: 10.3389/fped.2020.00385. eCollection 2020.
2
Global incidence of Necrotizing Enterocolitis: a systematic review and Meta-analysis.坏死性小肠结肠炎的全球发病率:一项系统评价和Meta分析
BMC Pediatr. 2020 Jul 13;20(1):344. doi: 10.1186/s12887-020-02231-5.
3
Association of Histological and Clinical Chorioamnionitis With Neonatal Sepsis Among Preterm Infants: A Systematic Review, Meta-Analysis, and Meta-Regression.组织学和临床绒毛膜羊膜炎与早产儿新生儿败血症的关系:系统评价、荟萃分析和荟萃回归。
Front Immunol. 2020 Jun 5;11:972. doi: 10.3389/fimmu.2020.00972. eCollection 2020.
4
Immediate Post-operative Enterocyte Injury, as Determined by Increased Circulating Intestinal Fatty Acid Binding Protein, Is Associated With Subsequent Development of Necrotizing Enterocolitis After Infant Cardiothoracic Surgery.通过循环中肠脂肪酸结合蛋白增加来确定的术后即刻肠上皮细胞损伤,与婴儿心胸外科手术后坏死性小肠结肠炎的后续发生相关。
Front Pediatr. 2020 May 27;8:267. doi: 10.3389/fped.2020.00267. eCollection 2020.
5
Dysregulated Mucosal Immunity and Associated Pathogeneses in Preterm Neonates.早产儿黏膜免疫失调及其相关发病机制。
Front Immunol. 2020 May 15;11:899. doi: 10.3389/fimmu.2020.00899. eCollection 2020.
6
Incidence, Treatment, and Outcome Trends of Necrotizing Enterocolitis in Preterm Infants: A Multicenter Cohort Study.早产儿坏死性小肠结肠炎的发病率、治疗及转归趋势:一项多中心队列研究
Front Pediatr. 2020 May 13;8:188. doi: 10.3389/fped.2020.00188. eCollection 2020.
7
Risk Factors for Necrotizing Enterocolitis in Infants With Patent Arterial Duct. A Retrospective Matched Paired Analysis.动脉导管未闭婴儿坏死性小肠结肠炎的危险因素。一项回顾性配对分析。
Front Pediatr. 2020 Apr 28;8:179. doi: 10.3389/fped.2020.00179. eCollection 2020.
8
Progressive Metabolic Dysfunction and Nutritional Variability Precedes Necrotizing Enterocolitis.进行性代谢功能障碍和营养变化先于坏死性小肠结肠炎。
Nutrients. 2020 Apr 30;12(5):1275. doi: 10.3390/nu12051275.
9
The Urinary Metabolome of Healthy Newborns.健康新生儿的尿液代谢组
Metabolites. 2020 Apr 23;10(4):165. doi: 10.3390/metabo10040165.
10
Postnatal Gut Immunity and Microbiota Development Is Minimally Affected by Prenatal Inflammation in Preterm Pigs.早产儿产前炎症对肠道免疫和微生物群发育的影响较小。
Front Immunol. 2020 Mar 19;11:420. doi: 10.3389/fimmu.2020.00420. eCollection 2020.

代谢组学和蛋白质组学时代坏死性小肠结肠炎预测与早期诊断的新兴生物标志物

Emerging Biomarkers for Prediction and Early Diagnosis of Necrotizing Enterocolitis in the Era of Metabolomics and Proteomics.

作者信息

Agakidou Eleni, Agakidis Charalampos, Gika Helen, Sarafidis Kosmas

机构信息

1st Department of Neonatology, Faculty of Medicine, Ippokration General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.

1st Department of Pediatrics, Faculty of Medicine, Ippokration General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.

出版信息

Front Pediatr. 2020 Dec 8;8:602255. doi: 10.3389/fped.2020.602255. eCollection 2020.

DOI:10.3389/fped.2020.602255
PMID:33425815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7793899/
Abstract

Necrotizing Enterocolitis (NEC) is a catastrophic disease affecting predominantly premature infants and is characterized by high mortality and serious long-term consequences. Traditionally, diagnosis of NEC is based on clinical and radiological findings, which, however, are non-specific for NEC, thus confusing differential diagnosis of other conditions such as neonatal sepsis and spontaneous intestinal perforation. In addition, by the time clinical and radiological findings become apparent, NEC has already progressed to an advanced stage. During the last three decades, a lot of research has focused on the discovery of biomarkers, which could accurately predict and make an early diagnosis of NEC. Biomarkers used thus far in clinical practice include acute phase proteins, inflammation mediators, and molecules involved in the immune response. However, none has been proven accurate enough to predict and make an early diagnosis of NEC or discriminate clinical from surgical NEC or other non-NEC gastrointestinal diseases. Complexity of mechanisms involved in NEC pathogenesis, which remains largely poorly elucidated, could partly explain the unsatisfactory diagnostic performance of the existing NEC biomarkers. More recently applied technics can provide important insight into the pathophysiological mechanisms underlying NEC but can also aid the detection of potentially predictive, early diagnostic, and prognostic biomarkers. Progress in omics technology has allowed for the simultaneous measurement of a large number of proteins, metabolic products, lipids, and genes, using serum/plasma, urine, feces, tissues, and other biological specimens. This review is an update of current data on emerging NEC biomarkers detected using proteomics and metabolomics, further discussing limitations and future perspectives in prediction and early diagnosis of NEC.

摘要

坏死性小肠结肠炎(NEC)是一种主要影响早产儿的灾难性疾病,其特点是死亡率高且有严重的长期后果。传统上,NEC的诊断基于临床和影像学表现,然而,这些表现对NEC并不具有特异性,因此混淆了诸如新生儿败血症和自发性肠穿孔等其他病症的鉴别诊断。此外,当临床和影像学表现明显时,NEC已经进展到晚期。在过去三十年中,许多研究都集中在生物标志物的发现上,这些生物标志物可以准确预测并早期诊断NEC。目前临床实践中使用的生物标志物包括急性期蛋白、炎症介质和参与免疫反应的分子。然而,尚未有足够准确的生物标志物能够预测并早期诊断NEC,或区分临床型与外科型NEC或其他非NEC胃肠道疾病。NEC发病机制的复杂性在很大程度上仍未得到充分阐明,这可能部分解释了现有NEC生物标志物诊断性能不尽人意的原因。最近应用的技术可以为NEC潜在的病理生理机制提供重要见解,也有助于检测潜在的预测性、早期诊断性和预后性生物标志物。组学技术的进步使得能够使用血清/血浆、尿液、粪便、组织和其他生物标本同时测量大量蛋白质、代谢产物、脂质和基因。本综述是关于使用蛋白质组学和代谢组学检测到的新兴NEC生物标志物的最新数据更新,进一步讨论了NEC预测和早期诊断中的局限性及未来展望。