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Published on: May 4, 2020
The evolving pathophysiology of bronchopulmonary dysplasia
Namasivayam Ambalavanan1, Gail Deutsch2, Gloria Pryhuber3
1Division of Neonatology, Department of Pediatrics, University of Alabama, Birmingham, Alabama, United States.
Insights
Bronchopulmonary dysplasia (BPD) in preterm infants stems from abnormal lung development due to various factors. This review details BPD
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Developmental Biology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant complication in very preterm infants, characterized by impaired lung development.
- The condition arises from a complex interplay of placental dysfunction, oxidative stress, mechanical ventilation, nutritional deficits, and genetic factors affecting the immature lung.
- These insults disrupt normal lung structure and function, impacting alveoli, vasculature, and airways.
Purpose of the Study:
- To provide a comprehensive review of normal lung development processes.
- To elucidate the mechanisms by which these processes are disrupted in BPD.
- To discuss the histological, mechanical, and functional consequences of BPD.
Main Methods:
- This review synthesizes current knowledge on lung development and BPD pathogenesis.
- It integrates findings from molecular and cellular studies of normal and BPD-affected lungs.
- The review discusses established and emerging therapeutic strategies and long-term implications.
Main Results:
- BPD results from multifactorial insults to the developing lung, affecting multiple cell types and signaling pathways.
- Abnormal lung development in BPD leads to lasting deficits in lung structure, mechanics, and gas exchange.
- Recent research highlights specific molecular pathways involved in BPD pathogenesis.
Conclusions:
- Understanding the disrupted pathways in BPD offers insights into its pathogenesis.
- Targeting these pathways presents potential for novel therapeutic interventions.
- Abnormal lung development in BPD has significant long-term consequences for respiratory health into adulthood.
Abstract:
Bronchopulmonary dysplasia (BPD) is the most common morbidity in very preterm infants and is characterized by abnormal development of the lung. The pathophysiology of BPD is primarily due to the effects of placental dysfunction, hyperoxia, ventilator-induced lung injury, poor nutrition, abnormal blood flow, and genomic/epigenomic factors on an immature lung. These adverse factors act on multiple cell types through many interacting signaling pathways. Abnormal development impacts most structures of the lung, including the alveoli, blood vessels, and airways, and frequently results in long-term impairment of lung mechanics and function. In this review, we provide a detailed overview of the processes involved in lung development and function and how these pathways are disrupted in BPD. The resulting effects on lung histology and lung mechanics and gas exchange are described. Insights derived from recent molecular and cellular characterization of lungs derived from normal and BPD-affected infants indicate possible mechanisms of pathogenesis and suggest potential new therapeutic strategies. The long-term implications of abnormal lung development as seen in BPD on later childhood and adult life are discussed.
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