# Arterialized oxygen tension and unfavorable clinical outcomes in pediatric cystic fibrosis

**Authors:** René Gaupmann, Saskia Gruber, Klara Schmidthaler, Bianca Pauger, Brigitte Mersi, Alexandra Graf, Zsolt Szépfalusi, Sabine Renner, Eleonora Dehlink

PMC · DOI: 10.3389/fped.2025.1653323 · Frontiers in Pediatrics · 2025-10-08

## TL;DR

Low oxygen levels in young cystic fibrosis patients predict faster lung function decline and more complications, suggesting a need for early monitoring.

## Contribution

Arterialized oxygen tension at age 5 is shown to predict future lung function decline and CF-related complications beyond spirometry.

## Key findings

- Low pO2 at age 5 correlates with accelerated FEV1 decline in CF patients.
- Early low pO2 increases the risk of allergic bronchopulmonary aspergillosis and other CF-related complications.
- pO2 is inversely related to lung clearance index and positively to FEV1.

## Abstract

Maintaining good lung function is a primary goal in managing Cystic Fibrosis (CF). As spirometry lacks sensitivity for detecting mild lung disease, early progression often remains unrecognized. To overcome this limitation, more sensitive monitoring tools are needed. We evaluated arterialized oxygen tension (pO2) as an easily accessible, and widely applicable surveillance method.

In this retrospective observational single-center cohort study, arterialized gas exchange was assessed in 103 young people with CF (47 females, 56 males, aged 5–18 years). Trends from baseline (age 5 years) to early adulthood and performance relative to annual best pulmonary function (FEV1) and lung clearance index were examined, along with baseline oxygen tension's predictive value on future FEV1 decline and the occurrence of CF-related complications.

pO2 correlated significantly with FEV1 (p < 0.001) and inversely with lung clearance index (p < 0.001). Higher pO₂ was associated with pancreatic sufficiency (p = 0.069) and dual CFTR modulator use (p < 0.05), with no differences by sex or chronic Pseudomonas aeruginosa infection. By age 5, 19.8% of young individuals with CF had pO₂ below 80 mmHg (5th percentile), of whom 73.7% had normal FEV1. A linear mixed model showed a steeper FEV1 decline in those with abnormal pO2 at baseline [estimate = 0.06 (Z-score*year−1), p < 0.001]. Early low pO2 was significantly associated with a higher probability of allergic bronchopulmonary aspergillosis (HR = 7.69, p = 0.016) and a trend towards early CF-related diabetes (HR = 2.78, p = 0.06) and early chronic Pseudomonas aeruginosa infection (HR = 2.38, p = 0.09).

Early abnormal pO2 at age 5 significantly correlated with accelerated FEV1 decline and a greater probability for CF-related complications. Implementing arterialized oxygen tension may offer valuable insights beyond spirometry alone in identifying high-risk patients.

## Linked entities

- **Diseases:** Cystic Fibrosis (MONDO:0009061), allergic bronchopulmonary aspergillosis (MONDO:0015243), CF-related diabetes (MONDO:7770003)

## Full-text entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** CF (MESH:D003550), allergic bronchopulmonary aspergillosis (MESH:D001229), Pseudomonas aeruginosa infection (MESH:D011552), pancreatic sufficiency (MESH:D010195), lung disease (MESH:D008171)
- **Chemicals:** oxygen (MESH:D010100), pO2 (MESH:C093415)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12540158/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12540158/full.md

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Source: https://tomesphere.com/paper/PMC12540158