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The Future of Bronchopulmonary Dysplasia: Emerging Pathophysiological Concepts and Potential New Avenues of Treatment

机译:支气管肺发育不良的未来:新兴的病理生理学概念和潜在的新治疗途径

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摘要

Yearly more than 15 million babies are born premature (<37 weeks gestational age), accounting for more than 1 in 10 births worldwide. Lung injury caused by maternal chorioamnionitis or preeclampsia, postnatal ventilation, hyperoxia, or inflammation can lead to the development of bronchopulmonary dysplasia (BPD), one of the most common adverse outcomes in these preterm neonates. BPD patients have an arrest in alveolar and microvascular development and more frequently develop asthma and early-onset emphysema as they age. Understanding how the alveoli develop, and repair, and regenerate after injury is critical for the development of therapies, as unfortunately there is still no cure for BPD. In this review, we aim to provide an overview of emerging new concepts in the understanding of perinatal lung development and injury from a molecular and cellular point of view and how this is paving the way for new therapeutic options to prevent or treat BPD, as well as a reflection on current treatment procedures.
机译:每年有超过1500万婴儿早产(小于37周),占全球十分之一的婴儿。由母亲绒毛膜羊膜炎或先兆子痫,产后通气,高氧血症或炎症引起的肺损伤可导致支气管肺发育不良(BPD)的发展,这是这些早产新生儿中最常见的不良后果之一。 BPD患者的肺泡和微血管发育停滞,并且随着年龄的增长更容易发生哮喘和早发性肺气肿。了解损伤后肺泡如何发育,修复和再生对于治疗的发展至关重要,因为不幸的是,目前尚无法治愈BPD。在这篇综述中,我们旨在从分子和细胞的角度概述围产期肺发育和损伤的新概念,以及如何为预防或治疗BPD的新治疗方法铺平道路。反映当前的治疗程序。

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