Effects of hyperoxia on oxygen uptake kinetics in cystic fibrosis patients as determined by pseudo-random binary sequence exercise

• Published in: European journal of applied physiology Vol. 79; no. 2; pp. 192 - 196
• Main Authors: KUSENBACH, G, WIECHING, R, BARKER, M, HOFFMANN, U, ESSFELD, D
• Format: Journal Article
• Language: English
• Published: Berlin Springer 1999
• Subjects: Adolescent; Adult; Biological and medical sciences; Child; Cystic Fibrosis - physiopathology; Exercise - physiology; Female; Gastroenterology. Liver. Pancreas. Abdomen; Humans; Hyperoxia - blood; Kinetics; Male; Medical sciences; Other diseases. Semiology; Oxygen Consumption - physiology; Pulmonary Gas Exchange - physiology; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Physical exercise; Human; Oxygen; Respiratory disease; Hyperoxia; Digestive diseases; Metabolic diseases; Cystic fibrosis; Kinetics; Uptake; Genetic disease; Pancreatic disease
• DOI: 10.1007/s004210050494
• ISSN: 0301-5548; 1439-6319

Patients with cystic fibrosis (CF) have been shown to exhibit impaired oxygen uptake (VO2) kinetics independent of their physical fitness. This study investigated whether oxygen supplementation improves VO2 kinetics in CF as determined by cycle ergometry at submaximal exercise intensities using a pseudo-random binary sequence exercise test i.e. a simultaneous application of different frequencies of sinusoidal work. The subjects were 9 CF patients and 13 healthy controls (HC) and they exercised while breathing humidified and heated air with a fractional concentration of oxygen in inspired air (F(I)O2) of either 0.21 or 0.40. With a F(I)O2 of 0.21 the respiratory exchange ratio (R) was higher in CF than in HC both at rest (0.91 vs 0.81) and during exercise (0.97 vs 0.89). Oxygen saturation (SO2) was slightly lower in CF. but remained above 90% during exercise (92.7% vs 95.2%). Spectrum analysis revealed that in CF, the amplitude ratio (AR) between V02 and exercise intensity was lower over a wide frequency range (P < 0.05). In addition, CF showed a larger negative phase shift (PS) at lower frequencies (P < 0.005). With a F(I)O2 of 0.40, SO2 increased to about 97% in both groups; while R remained higher in CF (0.92) compared to HC (0.81). In the control group, the O2 supplement raised AR but the VO, kinetics of the CF patients were not significantly affected. In HC the enhanced AR during oxygen supplementation would suggest a cardiopulmonary limitation of VO2 at the onset of submaximal exercise. In CF patients low AR and PS would indicate an attenuated VO2 response attributable to an impaired oxygen utilization in the muscles because the oxygen supplement normalised SO2 but failed to improve R and VO2 kinetics.