Machine learning-based risk prediction models for bronchopulmonary dysplasia in preterm infants: a high-altitude

Heng Zhang1, Fei Wang1, Ou Jiang1

  • 1Faculty of Medicine of Kunming University of Science and Technology, Kunming, Yunnan Province, China.

BMJ Paediatrics Open
|July 14, 2025
PubMed

Insights

This study identifies key risk factors for bronchopulmonary dysplasia (BPD) in high-altitude preterm infants. Machine learning models accurately predict BPD, enabling early interventions for better outcomes.

Area of Science:

  • Neonatology
  • Pediatric Respiratory Medicine
  • High-Altitude Physiology

Background:

  • Bronchopulmonary dysplasia (BPD) is a major cause of morbidity in preterm infants.
  • BPD development and severity at high altitudes (>1500m) are poorly understood.
  • This study addresses the knowledge gap by investigating altitude-specific risk factors.

Purpose of the Study:

  • Identify altitude-specific risk factors for BPD in preterm infants.
  • Develop and validate interpretable machine learning models for BPD prediction.
  • Inform early interventions to improve outcomes for high-altitude preterm infants.

Main Methods:

  • Retrospective matched cohort study of 378 preterm infants (<32 weeks gestation) at high altitude (1500m).
  • Collected maternal, perinatal, and postnatal data for 189 BPD cases and 189 controls.
  • Developed and evaluated XGBoost, logistic regression, and random forest models using SHAP analysis for interpretation.

Main Results:

  • Key risk factors for BPD: maternal hypertension, initial oxygen >30%, and lack of breast milk feeding.
  • Severe BPD associated with prolonged ventilation, elevated C-reactive protein, and PDA.
  • XGBoost model achieved AUC 0.89, F1 0.82, MCC 0.73, balanced accuracy 0.85.

Conclusions:

  • First comprehensive analysis of BPD risk factors at high altitude.
  • Validated effective and interpretable machine learning models for BPD prediction.
  • Emphasizes altitude-specific risk assessment and model-guided interventions for vulnerable infants.
Abstract

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