Early-life serum protein profiles associated with bronchopulmonary dysplasia in extremely preterm infants.

Respir ResSep 18, 2026 (epub)
Clinical ResearchPediatricsPulmonologyOpen access

Susanna Klevebro, Mohit B Panwar, Dirk Wackernagel et al.

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In 30 seconds

This multicenter randomized controlled trial studied early serum protein profiles in 176 extremely preterm infants (<28 weeks gestational age) to identify associations with bronchopulmonary dysplasia (BPD). The analysis revealed that 108 proteins exhibited distinct trajectories in infants with BPD, highlighting potential immune-related mechanisms involved in its pathogenesis.

Key findings

  • 108 out of 538 analyzed proteins showed distinct trajectories in infants with BPD.
  • Lower levels of Secretoglobin family 3A member 1 (SCGB3A1) and higher intercellular adhesion molecule 1 (ICAM-1) were associated with BPD.
  • Novel findings included lower levels of Leukocyte differentiation antigen CD84 in BPD infants.

Why it matters

Understanding the early serum protein profiles associated with BPD can help identify potential biomarkers and therapeutic targets. This knowledge may inform strategies to mitigate inflammation and improve outcomes in extremely preterm infants.

Source

Published in Respir Res. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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