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Published on: January 28, 2020
Longitudinal determinants of peak aerobic performance in children with cystic fibrosis
Peter H C Klijn1, Janjaap van der Net, Jan L Kimpen
1Departments of Pediatric Physical Therapy, Wilhelmina Children's Hospital, University Medical Center Utrecht, 3508 AB Utrecht, The Netherlands.
Insights
In children with cystic fibrosis (CF), changes in lung function and nutritional status longitudinally impact peak aerobic capacity (peak oxygen uptake). Exercise and nutrition interventions may improve long-term outcomes.
Area of Science:
- Pediatric Pulmonology
- Exercise Physiology
- Nutritional Science
Background:
- Cross-sectional studies link nutritional status and lung function to peak aerobic capacity in cystic fibrosis (CF).
- Longitudinal relationships between these factors in pediatric CF populations require further investigation.
Purpose of the Study:
- To determine the longitudinal relationship between changes in nutritional status, lung function, and peak aerobic capacity (peak oxygen uptake [O(2)peak]) in children with CF.
- To identify key predictors of changes in O(2)peak over a two-year period.
Main Methods:
- Assessed fat-free mass (FFM), lung function (FEV(1)), and O(2)peak in 65 children with CF at baseline and after 2 years.
- Utilized skinfold thickness for FFM calculation and age-appropriate incremental exercise testing for O(2)peak.
- Measured lung function prior to exercise testing.
Main Results:
- Observed significant increases in absolute FFM, FEV(1), and O(2)peak over two years.
- Noted decreases in predicted FEV(1) and O(2)peak values.
- Change in O(2)peak correlated most strongly with change in FEV(1) (r=0.619) and secondarily with change in FFM (r=0.506).
- FEV(1) and FFM changes explained 47% of the variation in O(2)peak changes.
Conclusions:
- Longitudinal changes in peak oxygen uptake in children with CF are associated with concurrent changes in lung function and, to a lesser extent, nutritional status.
- Exercise training and nutritional interventions are recommended to potentially enhance long-term clinical outcomes in pediatric CF patients.
Background:
Several cross-sectional studies in patients with cystic fibrosis (CF) have shown that nutritional status and lung function are important determinants of peak aerobic capacity (peak oxygen uptake [O(2)peak]). In order to account for individual changes, the aim of this study was to determine the longitudinal relationship of changes in nutritional status, lung function, and O(2)peak in children with CF.
Design And Methods:
Fat-free mass (FFM), lung function, and O(2)peak were assessed in 65 children with CF at baseline (mean +/- SD age, 10.5 +/- 2.9 years; mean FEV(1), 92.6 +/- 20.5%) and again 2 years later. FFM was calculated using skinfold thickness, and O(2)peak was measured using an incremental treadmill test for children < 12 years old or an incremental cycle ergometry test for children > or =12 years old. Lung function was measured before the exercise test.
Results:
Over the 2-year study period, an increase was found for absolute values of FFM (6.1 kg, p < 0.001), FEV(1) (229 mL, p < 0.001), and O(2)peak (240 mL, p < 0.001), while a decrease was found for predicted values of FEV(1) (- 8.9%, p < 0.001) and O(2)peak (- 4.4%, p < 0.05). DeltaO(2)peak over the 2-year period best correlated with DeltaFEV(1) (r = 0.619, p < 0.001) and to a lesser degree with DeltaFFM (r = 0.506, p < 0.001). Multiple regression analysis demonstrated that DeltaFEV(1) and DeltaFFM explained 47% of the variation of the DeltaO(2)peak over the 2-year period.
Conclusions:
Our results show that longitudinal changes in O(2)peak are associated with changes in lung function and to a lesser extent with changes in nutritional status in children with CF. Special consideration should be given to exercise training and nutritional intervention, which might improve long-term clinical outcome in children with CF.
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