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Updated: Jan 22, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
G Rocha1, F Flor de Lima1,2, A Paula Machado3
1Department of Neonatology, Centro Hospitalar São João, Porto, Portugal.
Insights
Small for gestational age (SGA) infants are significantly more likely to develop bronchopulmonary dysplasia (BPD). This study confirms SGA as an independent risk factor for BPD in preterm infants.
Area of Science:
- Neonatalogy
- Perinatal Medicine
- Pediatric Pulmonology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant concern in preterm infants.
- Previous studies have yielded mixed results on the association between low birth weight and BPD.
- This study aimed to clarify the link between low birth weight and BPD in a Portuguese cohort.
Purpose of the Study:
- To investigate the association between small for gestational age (SGA) and the development of bronchopulmonary dysplasia (BPD).
- To identify risk factors for BPD in preterm infants.
Main Methods:
- Prospective cohort study of preterm infants (24-30 weeks gestation) recruited from 11 Portuguese neonatal centers.
- Infants classified as SGA if birthweight was below the 10th percentile using Fenton's growth charts.
- BPD defined as oxygen dependency at 36 weeks corrected age; statistical analysis using logistic regression.
Main Results:
- Out of 494 infants, 8.0% were SGA.
- SGA infants had higher rates of BPD, periventricular leukomalacia, sepsis, and pneumonia.
- Multivariate analysis showed SGA is a significant independent risk factor for BPD (OR=5.2, p=0.01).
Conclusions:
- Small for gestational age is confirmed as an independent risk factor for bronchopulmonary dysplasia.
- Findings support closer monitoring and targeted interventions for SGA preterm infants.
- This research strengthens the evidence base for managing BPD risk in vulnerable neonates.
Introduction:
Several studies assessed the influence of a low birth weight on bronchopulmonary dysplasia (BPD), but not all could find a significant association. Our aim was to assess the association between low birth weight and BPD in preterm infants, prospectively recruited at 11 level III Portuguese neonatal centers.
Methods:
Obstetrical and neonatal data on mothers and preterm infants with gestational ages between 24 and 30 weeks, born during 2015 and 2016 after a surveilled pregnancy, were analyzed. Neonates were considered small for gestational age (SGA) when their birthweight was below the 10th centile of Fenton's growth chats and BPD was defined as the dependency for oxygen therapy until 36 weeks of corrected age. Statistical analysis was performed using IBM SPSS® statistics 23 and a p-value <0.05 was considered statistically significant.
Results:
Out of 614, a total of 494 preterm infants delivered from 410 women were enrolled in the study; 40 (8.0%) infants with SGA criteria. SGA were more often associated with a single pregnancy, had greater use of antenatal corticosteroids, increased prevalence of gestational hypertensive disorders, C-section, rupture of membranes below 18 hours, rate of intubation in the delivery room, use of surfactant treatment, oxygen therapy, mechanical ventilation need, BPD, cystic periventricular leukomalacia, nosocomial sepsis and pneumonia; had lower prevalence of chorioamnionitis, and lower Apgar scores. The multivariate analysis by logistic regression, adjusted for BPD risk factors revealed a significant association between SGA and BPD: OR = 5.2 [CI: 1.46-18.58]; p = 0.01.
Conclusion:
The results of this study increase the scientific evidence that SGA is an independent risk factor for BPD.
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