Department of Pediatrics, Division of Neonatal-Perinatal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Department of Pediatrics, Division of Neonatology, University of California, Davis, Sacramento, CA, USA.
J Perinatol. 2024 Nov;44(11):1552-1559. doi: 10.1038/s41372-024-02026-x. Epub 2024 Jun 6.
Necrotizing enterocolitis (NEC) continues to be a leading cause of morbidity and mortality in preterm infants. As modern medicine significantly improves the survival of extremely premature infants, the persistence of NEC underscores our limited understanding of its pathogenesis. Due to early delivery, a preterm infant's exposure to amniotic fluid (AF) is abruptly truncated. Replete with bioactive molecules, AF plays an important role in fetal intestinal maturation and preparation for contact with the environment, thus its absence during development of the intestine may contribute to increased susceptibility to NEC. Human milk (HM), particularly during the initial phases of lactation, is a cornerstone of neonatal intestinal defense. The concentrations and activities of several bioactive factors in HM parallel those of AF, suggesting continuity of protection. In this review, we discuss the predominant overlapping bioactive components of HM and AF, with an emphasis on those associated with intestinal growth or reduction of NEC.
新生儿坏死性小肠结肠炎(NEC)仍然是早产儿发病和死亡的主要原因。随着现代医学显著提高了极早产儿的存活率,NEC 的持续存在凸显了我们对其发病机制的有限理解。由于早产,早产儿接触羊水(AF)的时间突然中断。羊水富含生物活性分子,在胎儿肠道成熟和为接触环境做准备方面发挥着重要作用,因此在肠道发育过程中缺乏羊水可能会增加患 NEC 的易感性。人乳(HM),特别是在哺乳期的初始阶段,是新生儿肠道防御的基石。HM 中几种生物活性因子的浓度和活性与人 AF 相似,这表明保护作用具有连续性。在这篇综述中,我们讨论了 HM 和 AF 的主要重叠生物活性成分,重点是与肠道生长或减少 NEC 相关的成分。