新生儿坏死性小肠结肠炎血液样本中肠细胞DNA甲基化特征的检测。

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY Epigenomics Pub Date : 2025-03-01 Epub Date: 2025-02-02 DOI:10.1080/17501911.2025.2459552
Lauren Frazer, Tianjiao Chu, Patricia Shaw, Camille Boufford, Lucas Tavares Naief, Michaela Ednie, Laken Ritzert, Caitlin P Green, Misty Good, David Peters
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引用次数: 0

摘要

背景:坏死性小肠结肠炎(NEC)是一种通常致命的肠道损伤,主要影响缺乏筛查工具的早产儿。我们对患有和不患有NEC的早产儿外周血样本的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:采集NEC诊断婴儿(n = 15)或早产儿对照组(n = 13)外周血标本。进行有针对性的全基因组分析以确定病例和对照组之间的DNA甲基化差异。结果:NEC病例和对照组在不同的基因组元素上存在广泛差异。手术NEC病例与对照组之间的差异通常与炎症有关。识别细胞类型特异性DNA特征的反褶积分析显示,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减少。结论:我们发现有NEC和没有NEC的早产儿外周血样本的DNA甲基化有显著差异。与对照组相比,NEC婴儿血液中回肠细胞特异性甲基化特征增加,手术病例中甲基化特征明显增加,这为进一步分析肠道DNA甲基化特征作为NEC的生物标志物提供了依据。
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Detection of an intestinal cell DNA methylation signature in blood samples from neonates with necrotizing enterocolitis.

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 (n = 15) or from preterm controls (n = 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.

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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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