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本文引用的文献

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Methods of identifying surgical Necrotizing Enterocolitis-a systematic review and meta-analysis.识别外科坏死性小肠结肠炎的方法——一项系统评价和荟萃分析
Pediatr Res. 2025 Jan;97(1):45-55. doi: 10.1038/s41390-024-03292-3. Epub 2024 Jun 7.
2
DNA methylation in necrotizing enterocolitis.坏死性小肠结肠炎中的 DNA 甲基化。
Expert Rev Mol Med. 2024 Apr 1;26:e16. doi: 10.1017/erm.2024.16.
3
Integration of gene expression and DNA methylation data across different experiments.整合不同实验中的基因表达和 DNA 甲基化数据。
Nucleic Acids Res. 2023 Aug 25;51(15):7762-7776. doi: 10.1093/nar/gkad566.
4
Identification of serum biomarkers for necrotizing enterocolitis using aptamer-based proteomics.使用基于适配体的蛋白质组学鉴定坏死性小肠结肠炎的血清生物标志物
Front Pediatr. 2023 May 31;11:1184940. doi: 10.3389/fped.2023.1184940. eCollection 2023.
5
Fecal Keratin 8 Is a Noninvasive and Specific Marker for Intestinal Injury in Necrotizing Enterocolitis.粪便角蛋白 8 是坏死性小肠结肠炎肠损伤的一种非侵入性和特异性标志物。
J Immunol Res. 2023 Mar 14;2023:5356646. doi: 10.1155/2023/5356646. eCollection 2023.
6
Epigenetic Immune Cell Counting to Analyze Potential Biomarkers in Preterm Infants: A Proof of Principle in Necrotizing Enterocolitis.基于表观遗传的免疫细胞计数分析早产儿潜在生物标志物:以坏死性小肠结肠炎为例的原理验证。
Int J Mol Sci. 2023 Jan 25;24(3):2372. doi: 10.3390/ijms24032372.
7
Biomarkers of necrotizing enterocolitis in the era of machine learning and omics.基于机器学习和组学的坏死性小肠结肠炎生物标志物。
Semin Perinatol. 2023 Feb;47(1):151693. doi: 10.1016/j.semperi.2022.151693. Epub 2022 Dec 21.
8
A DNA methylation atlas of normal human cell types.正常人类细胞类型的 DNA 甲基化图谱。
Nature. 2023 Jan;613(7943):355-364. doi: 10.1038/s41586-022-05580-6. Epub 2023 Jan 4.
9
Selective hypermethylation is evident in small intestine samples from infants with necrotizing enterocolitis.选择性高甲基化在患有坏死性小肠结肠炎的婴儿的小肠样本中是明显的。
Clin Epigenetics. 2022 Apr 11;14(1):49. doi: 10.1186/s13148-022-01266-y.
10
Evaluation of the Neonatal Sequential Organ Failure Assessment and Mortality Risk in Preterm Infants with Necrotizing Enterocolitis.评估新生儿序贯器官衰竭评估和坏死性小肠结肠炎早产儿的死亡率。
Neonatology. 2022;119(3):334-344. doi: 10.1159/000522560. Epub 2022 Mar 21.

在坏死性小肠结肠炎新生儿血液样本中检测肠道细胞DNA甲基化特征

Detection of an intestinal cell DNA methylation signature in blood samples from neonates with necrotizing enterocolitis.

作者信息

Frazer Lauren, Chu Tianjiao, Shaw Patricia, Boufford Camille, Naief Lucas Tavares, Ednie Michaela, Ritzert Laken, Green Caitlin P, Good Misty, Peters David

机构信息

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Departments of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Epigenomics. 2025 Mar;17(4):235-245. doi: 10.1080/17501911.2025.2459552. Epub 2025 Feb 2.

DOI:10.1080/17501911.2025.2459552
PMID:39894787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11853613/
Abstract

BACKGROUND

Necrotizing enterocolitis (NEC) is an often fatal intestinal injury that primarily affects preterm infants for which screening tools are lacking. We performed a pilot analysis of DNA methylation in peripheral blood samples from preterm infants with and without NEC to identify potential NEC biomarkers.

METHODS

Peripheral blood samples were collected from infants at NEC diagnosis ( = 15) or from preterm controls ( = 13). Targeted genome-wide analysis was performed to identify DNA methylation differences between cases and controls.

RESULTS

Broad differences between NEC cases and controls were identified in distinct genomic elements. Differences between surgical NEC cases and controls were frequently associated with inflammation. Deconvolution analysis to identify cell type-specific DNA signatures revealed increases in ileal, vascular endothelial, and cardiomyocyte cell type proportions and decreases in colonic and neuronal cell type proportions in blood from NEC cases relative to controls.

CONCLUSIONS

We identified marked differences in DNA methylation of peripheral blood samples from preterm infants with and without NEC. Increased ileal cell-specific methylation signatures in the blood of infants with NEC relative to controls, with a marked increase seen in surgical cases, provides rationale for further analysis of intestinal DNA methylation signatures as biomarkers of NEC.

摘要

背景

坏死性小肠结肠炎(NEC)是一种常致命的肠道损伤,主要影响早产儿,目前缺乏筛查工具。我们对患有和未患有NEC的早产儿外周血样本中的DNA甲基化进行了初步分析,以确定潜在的NEC生物标志物。

方法

在NEC诊断时从婴儿(n = 15)或早产对照婴儿(n = 13)中采集外周血样本。进行靶向全基因组分析以确定病例组和对照组之间的DNA甲基化差异。

结果

在不同的基因组元件中发现了NEC病例与对照之间的广泛差异。手术NEC病例与对照之间的差异常与炎症相关。用于识别细胞类型特异性DNA特征的反卷积分析显示,与对照组相比,NEC病例血液中回肠、血管内皮和心肌细胞类型比例增加,结肠和神经元细胞类型比例降低。

结论

我们发现患有和未患有NEC的早产儿外周血样本的DNA甲基化存在显著差异。与对照组相比,患有NEC的婴儿血液中回肠细胞特异性甲基化特征增加,手术病例中尤为明显,这为进一步分析肠道DNA甲基化特征作为NEC生物标志物提供了理论依据。