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Progress in understanding the pathogenesis of BPD using the baboon and sheep models
1Department of Pediatrics, University of Utah, School of Medicine, Salt Lake City, UT 84158-1289, USA. kurt.albertine@hsc.utah.edu
Insights
Bronchopulmonary dysplasia (BPD) in infants is a common lung disease. Large animal models, like preterm baboons and lambs, offer insights into BPD
Area of Science:
- Neonatal physiology
- Pulmonary medicine
- Chronic lung disease research
Background:
- Bronchopulmonary dysplasia (BPD) is a prevalent chronic lung disease in US infants.
- Increased survival of preterm infants with BPD necessitates understanding long-term pulmonary complications.
- These complications include impaired gas exchange, pulmonary hypertension, and airway resistance.
Purpose of the Study:
- To review insights from large-animal physiological models of neonatal chronic lung disease.
- To enhance understanding of the molecular pathogenic mechanisms underlying BPD.
- To propose an epigenetic hypothesis for BPD pathogenesis and its persistent morbidities.
Main Methods:
- Focus on physiological models using preterm baboons.
- Focus on physiological models using preterm lambs.
- Review of existing literature on neonatal chronic lung disease models.
Main Results:
- Large-animal models provide unique physiological insights into neonatal chronic lung disease.
- These models aid in elucidating the molecular mechanisms driving BPD.
- An epigenetic hypothesis is proposed for BPD development and its sequelae.
Conclusions:
- Preterm baboon and lamb models are valuable for studying BPD.
- These models facilitate a deeper understanding of BPD's molecular pathogenesis.
- Epigenetic mechanisms may play a significant role in BPD and its chronic pulmonary outcomes.
Abstract:
Bronchopulmonary dysplasia (BPD) is among the most common chronic lung diseases in infants in the US. Improved survival of preterm infants who developed BPD is becoming increasingly important because of the high risk for persistent pulmonary morbidities such as poor respiratory gas exchange, pulmonary hypertension, and excess airway expiratory resistance later in life. This review focuses on unique insights provided by the two large-animal, physiological models of neonatal chronic lung disease: preterm baboons and preterm lambs. The models' are valuable because they contribute to better understanding of the underlying molecular pathogenic mechanisms. An epigenetic hypothesis is proposed as a pathogenic mechanism for BPD and its persistent pulmonary morbidities.
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