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Published on: May 8, 2017
Lung inflammation and simulated airway resistance in infants with cystic fibrosis
Emily M DeBoer1, Julia S Kimbell2, Kaci Pickett3
1University of Colorado Anschutz Medical Campus, Aurora, CO, United States; Breathing Institute at Children's Hospital Colorado, Aurora, CO, United States.
Insights
Infants with cystic fibrosis (CF) show higher airway resistance than controls, as measured by computational fluid dynamics (CFD). This increased resistance may link to early airway inflammation in CF patients.
Area of Science:
- Pulmonary Medicine
- Medical Imaging
- Computational Biology
Background:
- Cystic fibrosis (CF) primarily affects small airways, but central airway involvement is also observed.
- Early detection of airway abnormalities in infants with CF is crucial for timely intervention.
- Computational fluid dynamics (CFD) offers a non-invasive method to assess airway function.
Purpose of the Study:
- To investigate if infants with CF exhibit higher central airway resistance compared to healthy controls using CFD.
- To determine the association between early airway inflammation and central airway resistance in infants with CF.
Main Methods:
- Central airway models were constructed from CT scans of 18 infants with CF and 7 controls.
- Computational fluid dynamics (CFD) simulations were used to estimate central airway resistance.
- Airway resistance was correlated with inflammatory markers from bronchoalveolar lavage (BAL) fluid.
Main Results:
- Airway resistance was significantly higher in CF infants compared to controls, even when models were simplified.
- Increased airway resistance in CF infants was associated with inflammatory markers detected approximately 8 months prior to CFD analysis.
- No association was found between airway resistance and inflammatory markers obtained concurrently.
Conclusions:
- Infants with CF demonstrate elevated central airway resistance, measurable via CFD modeling.
- Early airway inflammation may be a contributing factor to increased airway resistance in infants with CF.
- CFD modeling shows promise for assessing early airway changes in pediatric CF.
Abstract:
Cystic fibrosis (CF) is characterized by small airway disease; but central airways may also be affected. We hypothesized that airway resistance estimated from computational fluid dynamic (CFD) methodology in infants with CF was higher than controls and that early airway inflammation in infants with CF is associated with airway resistance. Central airway models with a median of 51 bronchial outlets per model (interquartile range 46,56) were created from chest computed tomography scans of 18 infants with CF and 7 controls. Steady state airflow into the trachea was simulated to estimate central airway resistance in each model. Airway resistance was increased in the full airway models of infants with CF versus controls and in models trimmed to 33 bronchi. Airway resistance was associated with markers of inflammation in bronchoalveolar lavage fluid obtained approximately 8 months earlier but not with markers obtained at the same time. In conclusion, airway resistance estimated by CFD modeling is increased in infants with CF compared to controls and may be related to early airway inflammation.
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