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强化人乳细胞对I期坏死性小肠结肠炎早产儿粪便代谢组和肠道微生物群的影响:一项初步研究

Impacts of Enriched Human Milk Cells on Fecal Metabolome and Gut Microbiome of Premature Infants with Stage I Necrotizing Enterocolitis: A Pilot Study.

作者信息

Hong Luyang, Zhang Lan, Zhou Qi, Li Shujuan, Han Junyan, Jiang Siyuan, Han Xiao, Yang Yi, Hong Shangyu, Cao Yun

机构信息

Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, 200032, China.

NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, 200032, China.

出版信息

Mol Nutr Food Res. 2022 Jan;66(1):e2100342. doi: 10.1002/mnfr.202100342. Epub 2021 Dec 3.

DOI:10.1002/mnfr.202100342
PMID:34788490
Abstract

SCOPE

Necrotizing enterocolitis (NEC) is a leading cause of morbidity and mortality in preterm infants, occurring more often in formula-fed infants than in breastfed infants. Recent animal studies have shown that cells in fresh breast milk survive in the newborns' digestive tract. However, no clinical studies have been conducted on the effects of human milk cells, and their biological roles in the infants' intestines remain unexplored.

METHODS AND RESULTS

Twenty premature infants are enrolled. Cells from fresh milk of their own mothers are enriched and fed to infants with Bell's Stage I NEC once a day for 7 days since the onset of NEC. Fecal samples are collected at enrollment and 2 weeks later. Fecal sphingolipids are observed to be enriched in NEC patients and positively correlated with calprotectin levels. After intervention with enriched human milk cells, inflammation-associated sphingolipids and microbiome profiles are altered and resembled those of the controls.

CONCLUSION

These preliminary findings reveal the potential impacts of enriched human milk cells on premature infants with Bell's Stage I NEC and provide insight into the roles of fecal sphingolipid metabolism in the neonates' intestinal inflammation. However, the limited sample size of the study indicates the need for further investigation.

摘要

范围

坏死性小肠结肠炎(NEC)是早产儿发病和死亡的主要原因,配方奶喂养的婴儿比母乳喂养的婴儿更常发生。最近的动物研究表明,新鲜母乳中的细胞可在新生儿消化道内存活。然而,尚未有关于人乳细胞作用的临床研究,其在婴儿肠道中的生物学作用仍未得到探索。

方法与结果

招募了20名早产儿。收集其母亲新鲜母乳中的细胞并进行富集,自坏死性小肠结肠炎发病起,每天一次喂食给处于贝尔I期坏死性小肠结肠炎的婴儿,持续7天。在入组时和2周后采集粪便样本。观察到坏死性小肠结肠炎患者粪便中的鞘脂含量增加,且与钙卫蛋白水平呈正相关。用富集的人乳细胞进行干预后,与炎症相关的鞘脂和微生物群谱发生改变,与对照组相似。

结论

这些初步研究结果揭示了富集的人乳细胞对处于贝尔I期坏死性小肠结肠炎的早产儿的潜在影响,并深入了解了粪便鞘脂代谢在新生儿肠道炎症中的作用。然而,该研究样本量有限,表明需要进一步研究。

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