Abstract
Purpose - To investigate the effects of mild-to-moderate cystic fibrosis (CF) on the pulmonary oxygen uptake (VO2) kinetics of 7 pediatric patients (13.5 +/- 2.8 y) versus 7 healthy matched controls (CON; 13.6 +/- 2.4 y). We hypothesized that CF would slow the VO2 kinetic response at the onset of moderate (MOD) and very heavy (VH) intensity cycling.
Methods - Changes in breath-by-breath VO2, near-infrared spectroscopy-derived muscle deoxygenation ([HHb]) at the m. vastus lateralis and thoracic bioelectrical impedance-derived heart rate, stroke volume index (SVI) and cardiac index (CI) were measured during repeat transitions to MOD (90% of the gas exchange threshold) and VH (Δ60%) intensity cycling exercise.
Results - During MOD, the phase II VO2 [tau] (p=0.84; effect size (ES) = 0.11) and overall mean response time (MRT) (p=0.52; ES=0.11) were not significantly slower in CF versus CON. However, during VH exercise, the phase II VO2 [tau] (p=0.02, ES=1.28) and MRT (p=0.01, ES=1.40) were significantly slower in CF. Cardiac function, central O2 delivery (SVI and CI) and muscle [HHb] kinetics were unaltered in CF. However, the arterial-venous O2 content difference (C(a-)VO2) was reduced during VH at 30 s (p=0.03, ES=0.37), with a trend for reduced levels at 0 s (p=0.07, ES=0.25), 60 s (p=0.05, ES=0.28) and 120 s (p=0.07, ES=0.25) in CF. Furthermore, ΔC(a-)VO2 significantly correlated with the VH phase II VO2 [tau] (r= -0.85; p=0.02) and MRT (r = -0.79; p=0.03) in CF only.
Conclusion - Impairments in muscle oxidative metabolism during constant work rate exercise are intensity-dependent in young people with mild-to-moderate CF. Specifically, VO2 kinetics are slowed during VH but not MOD cycling and appear to be mechanistically linked to impaired muscle O2 extraction and utilization.
Methods - Changes in breath-by-breath VO2, near-infrared spectroscopy-derived muscle deoxygenation ([HHb]) at the m. vastus lateralis and thoracic bioelectrical impedance-derived heart rate, stroke volume index (SVI) and cardiac index (CI) were measured during repeat transitions to MOD (90% of the gas exchange threshold) and VH (Δ60%) intensity cycling exercise.
Results - During MOD, the phase II VO2 [tau] (p=0.84; effect size (ES) = 0.11) and overall mean response time (MRT) (p=0.52; ES=0.11) were not significantly slower in CF versus CON. However, during VH exercise, the phase II VO2 [tau] (p=0.02, ES=1.28) and MRT (p=0.01, ES=1.40) were significantly slower in CF. Cardiac function, central O2 delivery (SVI and CI) and muscle [HHb] kinetics were unaltered in CF. However, the arterial-venous O2 content difference (C(a-)VO2) was reduced during VH at 30 s (p=0.03, ES=0.37), with a trend for reduced levels at 0 s (p=0.07, ES=0.25), 60 s (p=0.05, ES=0.28) and 120 s (p=0.07, ES=0.25) in CF. Furthermore, ΔC(a-)VO2 significantly correlated with the VH phase II VO2 [tau] (r= -0.85; p=0.02) and MRT (r = -0.79; p=0.03) in CF only.
Conclusion - Impairments in muscle oxidative metabolism during constant work rate exercise are intensity-dependent in young people with mild-to-moderate CF. Specifically, VO2 kinetics are slowed during VH but not MOD cycling and appear to be mechanistically linked to impaired muscle O2 extraction and utilization.
Original language | English |
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Pages (from-to) | 2090-2099 |
Journal | Medicine and Science in Sports & Exercise |
Volume | 48 |
Issue number | 11 |
Early online date | 9 Jun 2016 |
DOIs | |
Publication status | Published - Nov 2016 |
Keywords
- oxidative muscle metabolism
- pulmonary disease
- near-infrared spectroscopy
- oxygen delivery
- pediatrics