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Published on: March 17, 2014
Early airway infection, inflammation, and lung function in cystic fibrosis
G M Nixon1, D S Armstrong, R Carzino
1Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia. gillian.nixon@muhc.mcgill.ca
Insights
In young children with cystic fibrosis (CF), both respiratory symptoms and lower airway infections independently worsen lung function. Airway inflammation did not show a direct link to lung function decline in this study.
Area of Science:
- Pediatric Pulmonology
- Cystic Fibrosis Research
- Respiratory Medicine
Background:
- Cystic Fibrosis (CF) affects multiple organs, particularly the lungs.
- Early detection and monitoring of lung health in infants and young children with CF are crucial.
- Understanding factors influencing lung function in early CF is essential for timely intervention.
Purpose of the Study:
- To investigate the relationship between lower airway infection, inflammation, and respiratory symptoms with lung function in young children with CF.
- To assess the impact of infection and inflammation on lung function parameters.
- To determine if respiratory symptoms correlate with objective measures of infection or inflammation.
Main Methods:
- Prospective study of children under 3 years old with CF diagnosed via newborn screening.
- Bronchial lavage (BL) for infection and inflammation markers (neutrophils, IL-8, elastase) and lung function testing (FEV) under general anesthesia.
- Correlation analysis between infection, inflammation markers, respiratory symptoms (cough), and lung function (FEV0.5, FEV0.75, FEV1).
Main Results:
- Lower airway infection was associated with a 10% reduction in FEV(0.5) in children with CF.
- No significant correlation was found between airway inflammation markers and lung function.
- Daily cough was linked to lower lung function, independent of infection or inflammation status.
Conclusions:
- Respiratory symptoms and lower airway infections independently and additively impact lung function in young children with CF.
- Airway inflammation does not appear to be a primary driver of lung function decline in this age group.
- Further research is required to elucidate the mechanisms of airway obstruction in early-stage CF.
Aims:
To determine the relation between lower airway infection and inflammation, respiratory symptoms, and lung function in infants and young children with cystic fibrosis (CF).
Methods:
A prospective study of children with CF aged younger than 3 years, diagnosed by a newborn screening programme. All were clinically stable and had testing as outpatients. Subjects underwent bronchial lavage (BL) and lung function testing by the raised volume rapid thoracoabdominal compression technique under general anaesthesia. BL fluid was cultured and analysed for neutrophil count, interleukin 8, and neutrophil elastase. Lung function was assessed by forced expiratory volume in 0.5, 0.75, and 1 second.
Results:
Thirty six children with CF were tested on 54 occasions. Lower airway infection shown by BL was associated with a 10% reduction in FEV(0.5) compared with subjects without infection. No relation was identified between airway inflammation and lung function. Daily moist cough within the week before testing was reported on 20/54 occasions, but in only seven (35%) was infection detected. Independent of either infection status or airway inflammation, those with daily cough had lower lung function than those without respiratory symptoms at the time of BL (mean adjusted FEV(0.5) 195 ml and 236 ml respectively).
Conclusions:
In young children with CF, both respiratory symptoms and airway infection have independent, additive effects on lung function, unrelated to airway inflammation. Further studies are needed to understand the mechanisms of airway obstruction in these young patients.
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