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Updated: Feb 18, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Chorioamnionitis is essential in the evolution of bronchopulmonary dysplasia--the case in favour
Wolfgang Thomas1, Christian P Speer2
1Mutterhaus der Borromaeerinnen, Department of Pediatrics, Feldstr. 6, 54290 Trier, Germany.
Insights
Chorioamnionitis, an infection during pregnancy, significantly increases the risk of bronchopulmonary dysplasia (BPD) in premature infants. This inflammation contributes to both preterm birth and direct lung injury, worsening BPD outcomes.
Area of Science:
- Neonatal Medicine
- Pulmonology
- Obstetrics
Background:
- Bronchopulmonary dysplasia (BPD) is a primary complication in extremely premature infants.
- Multiple factors contribute to BPD pathogenesis, with antenatal inflammation playing a crucial role.
Purpose of the Study:
- To elucidate the role of chorioamnionitis in the development of bronchopulmonary dysplasia.
- To analyze the association between chorioamnionitis and BPD risk in preterm neonates.
Main Methods:
- Review of current evidence and clinical observational studies.
- Analysis of animal models simulating chorioamnionitis and its pulmonary effects.
- Assessment of chorioamnionitis's impact on preterm birth and postnatal complications.
Main Results:
- Chorioamnionitis induces pulmonary inflammation similar to that observed in BPD.
- Chorioamnionitis is linked to both gestation-dependent and independent increases in BPD risk.
- Antenatal inflammation compromises surfactant response and necessitates prolonged mechanical ventilation.
Conclusions:
- Chorioamnionitis is a pivotal factor in BPD development, acting through preterm birth and direct lung injury.
- Early sepsis and mechanical ventilation, exacerbated by chorioamnionitis, are significant postnatal contributors to BPD.
Abstract:
Bronchopulmonary dysplasia (BPD) is a major sequel of extremely premature birth. Multiple ante- and postnatal factors act in concert to injure the immature lung in the pathogenesis of the disease. Among them, chorioamnionitis--according to current evidence--plays a pivotal role. Pulmonary inflammatory processes seen in animal models of chorioamnionitis resemble those seen in premature infants who developed BPD. Chorioamnionitis can doubtlessly induce extremely preterm birth, thus contributing to a gestation-dependent risk of BPD. A gestation-independent association of chorioamnionitis with an increased risk of developing BPD has been demonstrated by a recent systematic review of clinical observational studies. Antenatal inflammation with signs of a systemic fetal response reduces the response to exogenous surfactant in infants with respiratory distress syndrome, leading to a longer need for mechanical ventilation. Moreover, chorioamnionitis increases the risk of early onset sepsis. Both mechanical ventilation and sepsis are, however, major postnatal risk factors for BPD.
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