探讨早产儿坏死性小肠结肠炎的复杂病理生理学。

IF 34.5 1区 医学 Q1 PATHOLOGY
Bo Li,Mina Yeganeh,Dorothy Lee,Sinobol Chusilp,Felicia Balsamo,Niloofar Ganji,Chen-Yi Wang,Andrea Zito,George Biouss,Agostino Pierro
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引用次数: 0

摘要

坏死性小肠结肠炎(NEC)是早产儿最常见的胃肠道急症,晚期死亡率为30-50%。尽管经过数十年的研究,其多因素病理生理机制仍未完全了解。本文综述了NEC研究的最新进展,并提出了其发病机制的综合理论框架。我们研究了关键的影响因素,包括肠血管发育、粘膜免疫、肠道再生、肠神经系统和肠道微生物群,强调了早产如何破坏这些过程并使新生儿易患NEC。此外,我们提出了一个NEC发病机制的序列模型,假设早产儿肠道微循环受损会影响血液流动,从而导致局部缺血。这会引发上皮屏障功能障碍,加剧炎症反应,损害肠道再生,破坏肠神经系统功能,共同推动NEC的进展。通过整合实验和临床研究结果,我们提供了早产儿NEC发病的全面视角,并确定了未来研究和治疗干预的潜在途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the Complex Pathophysiology of Necrotizing Enterocolitis in Preterm Neonates.
Necrotizing enterocolitis (NEC) is the most common gastrointestinal emergency in preterm neonates, with a mortality rate of 30-50% in advanced cases. Despite decades of research, its multifactorial pathophysiology remains incompletely understood. This review summarizes recent advances in NEC research and proposes an integrative theoretical framework for its pathogenesis. We examine key contributing factors, including intestinal vascular development, mucosal immunity, intestinal regeneration, the enteric nervous system, and the gut microbiome, highlighting how prematurity disrupts these processes and predisposes neonates to NEC. Furthermore, we propose a sequential model of NEC pathogenesis, hypothesizing that impaired intestinal microcirculation in preterm neonates compromises blood flow in response to enteral feeding, leading to localized ischemia. This initiates epithelial barrier dysfunction, exacerbates inflammatory responses, impairs intestinal regeneration, and disrupts enteric nervous system function, collectively driving NEC progression. By integrating experimental and clinical findings, we provide a comprehensive perspective on NEC initiation in preterm neonates and identify potential avenues for future research and therapeutic interventions.
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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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