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Published on: January 6, 2015
Inhaled corticosteroids and lower lung function decline in young children with cystic fibrosis
K De Boeck1, F Vermeulen, S Wanyama
1Paediatric Pulmonology, University of Leuven, Leuven, Belgium.
Insights
Inhaled corticosteroid (ICS) use in children with cystic fibrosis (CF) was linked to slower lung function decline. This benefit was most significant in younger children aged 6-12 years.
Area of Science:
- Pulmonology
- Pediatrics
- Pharmacology
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting lung function.
- Previous studies suggested inhaled corticosteroids (ICS) may slow lung function decline in CF patients.
- The impact of ICS on lung function in Belgian CF patients required further investigation.
Purpose of the Study:
- To evaluate the effect of inhaled corticosteroid (ICS) treatment on lung function decline in Belgian cystic fibrosis (CF) patients.
- To compare lung function changes in CF patients with and without ICS use.
- To identify age-specific effects of ICS on CF lung function.
Main Methods:
- Retrospective analysis of data from Belgian CF patients aged 6 years and older.
- Inclusion criteria: consecutive yearly data on lung function, height, and ICS use.
- Exclusion criteria: data following oral steroid use or lung transplantation.
- Analysis of 2,976 data pairs from 852 subjects, with 44.9% representing years of ICS use.
Main Results:
- Yearly decline in forced expiratory volume in 1 second (FEV₁) was 1.07% lower in patients using ICS (p = 0.001).
- This reduced FEV₁ decline was statistically significant in children aged 6-12 years (2.56% lower, p = 0.0003).
- While overall ICS users had lower baseline FEV₁, this difference was not observed in the 6-12 year age group.
Conclusions:
- Inhaled corticosteroid (ICS) use is associated with a slower rate of lung function decline in children with cystic fibrosis (CF).
- The protective effect of ICS on lung function is particularly pronounced in younger children (6-12 years).
- Findings support previous registry analyses and suggest ICS as a beneficial treatment for lung function in pediatric CF patients.
Abstract:
A recent American registry analysis in cystic fibrosis (CF) children showed less lung function decline after starting inhaled corticosteroid (ICS) use. We therefore examined the influence of ICS treatment on lung function in Belgian CF patients. Data from patients ≥ 6 yrs of age were eligible, provided entries on lung function, height and ICS use were available in two consecutive years. Data after oral steroid use or transplant were excluded. 852 subjects contributed data with 2,976 data pairs analysed, 44.9% concerning years of ICS use. Yearly % predicted decline in forced expiratory volume in 1 s (FEV₁) was 1.07% lower during ICS use (p = 0.001). Subgroup analysis for age revealed that the lower FEV₁ decline rate during ICS use was only statistically significant in children 6-12 yrs of age (2.56%; p = 0.0003). Baseline FEV(1) was lower by 5.89% (p < 0.0001) in ICS users for all age groups combined, but there was no difference in baseline lung function in the children 6-12 yrs of age. In 6-12-yr-old children with CF, baseline lung function was similar in ICS users and nonusers, but annualised FEV₁ decline was 2.56% pred lower in ICS users. Our data therefore support recent American findings.
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