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Looking beyond bronchopulmonary dysplasia: prematurity-associated lung disease and its phenotypes
Christopher William Course1, Andrew Bush2, Sailesh Kotecha1
1Department of Child Health, School of Medicine, Cardiff University, Cardiff, UK.
Insights
Preterm birth is a key factor in chronic respiratory diseases. This study introduces prematurity-associated lung disease (PLD) as a framework to understand diverse lung issues in preterm infants, aiding personalized care.
Area of Science:
- Pulmonology
- Neonatology
- Pediatric Respiratory Medicine
Background:
- Preterm birth is a significant risk factor for chronic respiratory diseases throughout life.
- Historically, focus has been on extremely preterm infants and bronchopulmonary dysplasia (BPD), but other preterm groups also face lung disease risks.
- Factors beyond BPD, including gestational age and intrauterine growth restriction, contribute to lung disease in preterm infants.
Purpose of the Study:
- To introduce prematurity-associated lung disease (PLD) as a unifying concept for pulmonary consequences of preterm birth.
- To highlight diverse PLD phenotypes beyond traditional BPD.
- To establish a foundation for personalized monitoring and targeted therapies for preterm infants with lung disease.
Main Methods:
- Review and synthesis of existing literature on lung disease following preterm birth.
- Identification and characterization of distinct prematurity-associated lung disease phenotypes.
- Analysis of contributing factors and prognostic implications for each phenotype.
Main Results:
- Preterm birth is a determinant of chronic respiratory disease across the lifespan.
- Multiple phenotypes of prematurity-associated lung disease (PLD) exist, including obstructive lung disease, preserved ratio impaired spirometry, and dysanapsis.
- These phenotypes are linked to specific early-life exposures and mechanisms, impacting prognosis differently.
Conclusions:
- PLD provides a comprehensive framework for understanding the spectrum of lung disease in preterm infants.
- Recognizing distinct PLD phenotypes is crucial for developing individualized management strategies.
- Further research into these phenotypes will enable more precise monitoring and therapeutic interventions for affected children.
Abstract:
Preterm birth is increasingly recognised as a determinant of chronic respiratory disease across the life course. In this Series on prematurity-associated lung disease (PLD), we introduce the concept of PLD as a unifying framework for the diverse pulmonary consequences of preterm birth. Historically, most attention has focused on extremely preterm infants (<28 weeks of gestation) who develop bronchopulmonary dysplasia (BPD), yet not all infants with BPD have long-term morbidity. Conversely, those born very (28-31 weeks), moderate (32-33 weeks), or late (34-36 weeks) preterm also have increased risk for developing lung disease. Multiple factors beyond BPD-including gestational age and intrauterine growth restriction-contribute to PLD development. Recently described PLD phenotypes include prematurity-associated obstructive lung disease, prematurity-associated preserved ratio impaired spirometry, and prematurity-associated dysanapsis. Each phenotype reflects distinct early-life exposures and mechanisms, with differing implications for prognosis. Defining these phenotypes provides a foundation for personalised monitoring and targeted therapeutic strategies.
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