Looking beyond bronchopulmonary dysplasia: prematurity-associated lung disease and its phenotypes

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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Publication Details

Journal
The Lancet Respiratory Medicine
Published
2025-11-27
DOI
https://doi.org/10.1016/s2213-2600(25)00372-8
Citations
1
Primary Topic
Neonatal Respiratory Health Research
Type
article
Field-Weighted Citation Impact
1.52
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article

Looking beyond bronchopulmonary dysplasia: prematurity-associated lung disease and its phenotypes

Sailesh Kotecha, Christopher W. Course, Andrew Bush
1 citations
The Lancet Respiratory Medicine
Neonatal Respiratory Health Research
1.52
article

Looking beyond bronchopulmonary dysplasia: prematurity-associated lung disease and its phenotypes

Sailesh Kotecha, Christopher W. Course, Andrew Bush
article en
1 citations

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.

The Lancet Respiratory MedicineVol. 14(1)
Imperial College London (GB), Royal College of Paediatrics and Child Health (GB), Cardiff University (GB)
Openalex Percentile: Top 12%
Neonatal Respiratory Health Research
1.52
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