Sahni Mitali, Bhandari Vineet
Pediatrix Medical Group, Sunrise Children's Hospital, Las Vegas, NV, USA.
University of Nevada, Las Vegas, NV, USA.
Mol Cell Pediatr. 2021 Dec 11;8(1):21. doi: 10.1186/s40348-021-00129-5.
Bronchopulmonary dysplasia (BPD) continues to be one of the most common complications of prematurity, despite significant advancement in neonatology over the last couple of decades. The new BPD is characterized histopathologically by impaired lung alveolarization and dysregulated vascularization. With the increased survival of extremely preterm infants, the risk for the development of BPD remains high, emphasizing the continued need to understand the patho-mechanisms that play a role in the development of this disease. This brief review summarizes recent advances in our understanding of the maldevelopment of the premature lung, highlighting recent research in pathways of oxidative stress-related lung injury, the role of placental insufficiency, growth factor signaling, the extracellular matrix, and microRNAs.
尽管在过去几十年新生儿学取得了显著进展,但支气管肺发育不良(BPD)仍然是早产最常见的并发症之一。新的BPD在组织病理学上的特征是肺泡化受损和血管生成失调。随着极早产儿存活率的提高,BPD发生的风险仍然很高,这突出表明持续需要了解在该疾病发生过程中起作用的病理机制。本简要综述总结了我们对早产肺发育异常认识的最新进展,重点介绍了氧化应激相关肺损伤途径、胎盘功能不全的作用、生长因子信号传导、细胞外基质和微小RNA的最新研究。