Long-term exercise capacity in paediatric cystic fibrosis: a modern era perspective

René Gaupmann1, Laura Stöger1, Klara Schmidthaler1

  • 1Department of Paediatrics, Division of Paediatric Pulmonology, Allergy and Endocrinology, Medical University of Vienna, Vienna, Austria.

ERJ Open Research
|July 9, 2025
PubMed

Insights

Cardiopulmonary fitness in cystic fibrosis (CF) is impaired during adolescence. However, treatment with elexacaftor, tezacaftor, and ivacaftor (ETI) significantly improves peak oxygen uptake in young people with CF.

Area of Science:

  • Cardiology
  • Pulmonology
  • Pediatrics

Background:

  • Cardiopulmonary fitness is vital for individuals with cystic fibrosis (CF).
  • Limited data exist on fitness evolution in young CF patients, especially with new therapies.
  • Recent advances include elexacaftor, tezacaftor, and ivacaftor (ETI) and the COVID-19 pandemic.

Purpose of the Study:

  • To investigate longitudinal trends in exercise test outcomes in young people with CF.
  • To assess the influence of ETI and the COVID-19 pandemic on these trends.

Main Methods:

  • Retrospective observational study of 70 young people with CF (12-20 years).
  • Analysis of 177 cardiopulmonary exercise tests (CPETs) from 2010-2024.
  • Longitudinal trends in peak oxygen uptake (V'O2peak), maximal workload, and ventilation analyzed using mixed models.

Main Results:

  • ETI-naive CF patients showed lower V'O2peak than reference data.
  • Initiation of ETI significantly improved V'O2peak.
  • Ventilation and maximal workload were not significantly affected by ETI.
  • COVID-19 pandemic coincided with a steeper V'O2peak decline in ETI-naive patients, but did not negate ETI's positive impact.

Conclusions:

  • Cardiopulmonary fitness progression is impaired in adolescents with CF.
  • ETI therapy positively impacts the longitudinal trajectory of V'O2peak in young CF patients.
Abstract

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