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The Effects of Hyperoxia on Sea-Level Exercise Performance, Training, and Recovery: A Meta-Analysis

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Abstract

Background

Acute exercise performance can be limited by arterial hypoxemia, such that hyperoxia may be an ergogenic aid by increasing tissue oxygen availability. Hyperoxia during a single bout of exercise performance has been examined using many test modalities, including time trials (TTs), time to exhaustion (TTE), graded exercise tests (GXTs), and dynamic muscle function tests. Hyperoxia has also been used as a long-term training stimulus or a recovery intervention between bouts of exercise. However, due to the methodological differences in fraction of inspired oxygen (FiO2), exercise type, training regime, or recovery protocols, a firm consensus on the effectiveness of hyperoxia as an ergogenic aid for exercise training or recovery remains unclear.

Objectives

The aims of this study were to (1) determine the efficacy of hyperoxia as an ergogenic aid for exercise performance, training stimulus, and recovery before subsequent exercise; and (2) determine if a dose–response exists between FiO2 and exercise performance improvements.

Data Source

The PubMed, Web of Science, and SPORTDiscus databases were searched for original published articles up to and including 8 September 2017, using appropriate first- and second-order search terms.

Study Selection

English-language, peer-reviewed, full-text manuscripts using human participants were reviewed using the process identified in the preferred reporting items for systematic reviews and meta-analyses (PRISMA) statement.

Data Extraction

Data for the following variables were obtained by at least two of the authors: FiO2, wash-in time for gas, exercise performance modality, heart rate, cardiac output, stroke volume, oxygen saturation, arterial and/or capillary lactate, hemoglobin concentration, hematocrit, arterial pH, arterial oxygen content, arterial partial pressure of oxygen and carbon dioxide, consumption of oxygen and carbon dioxide, minute ventilation, tidal volume, respiratory frequency, ratings of perceived exertion of breathing and exercise, and end-tidal oxygen and carbon dioxide partial pressures.

Data Grouping

Data were grouped into type of intervention (acute exercise, recovery, and training), and performance data were grouped into type of exercise (TTs, TTE, GXTs, dynamic muscle function), recovery, and training in hyperoxia.

Data Analysis

Hedges’ g effect sizes and 95% confidence intervals were calculated. Separate Pearson’s correlations were performed comparing the effect size of performance versus FiO2, along with the effect size of arterial content of oxygen, arterial partial pressure of oxygen, and oxygen saturation.

Results

Fifty-one manuscripts were reviewed. The most common FiO2 for acute exercise was 1.00, with GXTs the most investigated exercise modality. Hyperoxia had a large effect improving TTE (g = 0.89), and small-to-moderate effects increasing TTs (g = 0.56), GXTs (g = 0.40), and dynamic muscle function performance (g = 0.28). An FiO2 ≥ 0.30 was sufficient to increase general exercise performance to a small effect or higher; a moderate positive correlation (r = 0.47–0.63) existed between performance improvement of TTs, TTE, and dynamic muscle function tests and FiO2, but not GXTs (r = 0.06). Exercise training and recovery supplemented with hyperoxia trended towards a large and small ergogenic effect, respectively, but the large variability and limited amount of research on these topics prevented a definitive conclusion.

Conclusion

Acute exercise performance is increased with hyperoxia. An FiO2 ≥ 0.30 appears to be beneficial for performance, with a higher FiO2 being correlated to greater performance improvement in TTs, TTE, and dynamic muscle function tests. Exercise training and recovery supplemented with hyperoxic gas appears to have a beneficial effect on subsequent exercise performance, but small sample size and wide disparity in experimental protocols preclude definitive conclusions.

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References

  1. Abbiss CR, Laursen PB. Models to explain fatigue during prolonged endurance cycling. Sports Med. 2005;35:865–98.

    Article  PubMed  Google Scholar 

  2. Dempsey JA, Amann M, Romer LM, et al. Respiratory system determinants of peripheral fatigue and endurance performance. Med Sci Sports Exerc. 2008;40:457–61.

    Article  PubMed  Google Scholar 

  3. Nybo L, Rasmussen P, Sawka MN. Performance in the heat-physiological factors of importance for hyperthermia-induced fatigue. Compr Physiol. 2014;4:657–89.

    Article  PubMed  Google Scholar 

  4. Dempsey JA, Wagner PD. Exercise-induced arterial hypoxemia. J Appl Physiol. 1985;1999(87):1997–2006.

    Google Scholar 

  5. Dempsey JA, Hanson PG, Henderson KS. Exercise-induced arterial hypoxaemia in healthy human subjects at sea level. J Physiol. 1984;355:161.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Nummela A, Hämäläinen I, Rusko H. Effect of hyperoxia on metabolic responses and recovery in intermittent exercise. Scand J Med Sci Sports. 2002;12:309–15.

    Article  CAS  PubMed  Google Scholar 

  7. Amann M, Eldridge MW, Lovering AT, et al. Arterial oxygenation influences central motor output and exercise performance via effects on peripheral locomotor muscle fatigue in humans. J Physiol. 2006;575:937–52.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Sperlich B, Zinner C, Hauser A, et al. The impact of hyperoxia on human performance and recovery. Sports Med. 2017;47:429–38.

    Article  PubMed  Google Scholar 

  9. Richardson RS, Grassi B, Gavin TP, et al. Evidence of O2 supply-dependent VO2 max in the exercise-trained human quadriceps. J Appl Physiol. 1985;1999(86):1048–53.

    Google Scholar 

  10. Casey DP, Joyner MJ, Claus PL, et al. Hyperbaric hyperoxia reduces exercising forearm blood flow in humans. Am J Physiol Heart Circ Physiol. 2011;300:H1892–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Casey DP, Joyner MJ, Claus PL, et al. Vasoconstrictor responsiveness during hyperbaric hyperoxia in contracting human muscle. J Appl Physiol. 1985;2013(114):217–24.

    Google Scholar 

  12. Richardson RS, Leigh JS, Wagner PD, et al. Cellular PO2 as a determinant of maximal mitochondrial O2consumption in trained human skeletal muscle. J Appl Physiol. 1985;1999(87):325–31.

    Google Scholar 

  13. Joyner MJ, Casey DP. Muscle blood flow, hypoxia, and hypoperfusion. J Appl Physiol. 1985;2014(116):852–7.

    Google Scholar 

  14. Stellingwerff T, LeBlanc PJ, Hollidge MG, et al. Hyperoxia decreases muscle glycogenolysis, lactate production, and lactate efflux during steady-state exercise. Am J Physiol Endocrinol Metab. 2006;290:E1180–90.

    Article  CAS  PubMed  Google Scholar 

  15. Pedersen P, Kiens B, Saltin B. Hyperoxia does not increase peak muscle oxygen uptake in small muscle group exercise. Acta Physiol Scand. 1999;166:309–18.

    Article  CAS  PubMed  Google Scholar 

  16. Oussaidene K, Prieur F, Bougault V, et al. Cerebral oxygenation during hyperoxia-induced increase in exercise tolerance for untrained men. Eur J Appl Physiol. 2013;113:2047–56.

    Article  PubMed  Google Scholar 

  17. Nielsen HB, Madsen RP, Secher NH. Cerebral desaturation during exercise reversed by O2 supplementation. Am J Physiol Heart Circ Physiol. 1999;277:H1045–52.

    Article  CAS  Google Scholar 

  18. Smith KJ, Wildfong KW, Hoiland RL, et al. Role of CO2 in the cerebral hyperemic response to incremental normoxic and hyperoxic exercise. J Appl Physiol. 1985;2016(120):843–54.

    Google Scholar 

  19. Nybo L. Hyperthermia and fatigue. J Appl Physiol. 1985;2008(104):871–8.

    Google Scholar 

  20. Bain AR, Nybo L, Ainslie PN. Cerebral vascular control and metabolism in heat stress. Compr Physiol. 2015;5:1345–80.

    Article  PubMed  Google Scholar 

  21. Smith KJ, Wong LE, Eves ND, et al. Regional cerebral blood flow distribution during exercise: influence of oxygen. Respir Physiol Neurobiol. 2012;184:97–105.

    Article  CAS  PubMed  Google Scholar 

  22. Stellingwerff T, Glazier M, Watt MJ, et al. Effects of hyperoxia on skeletal muscle carbohydrate metabolism during transient and steady-state exercise. J Appl Physiol. 1985;2005(98):250–6.

    Google Scholar 

  23. Yokoi Y, Yanagihashi R, Morishita K, et al. Recovery effects of repeated exposures to normobaric hyperoxia on local muscle fatigue. J Strength Cond Res. 2014;28:2173–9.

    Article  PubMed  Google Scholar 

  24. Peeling P, Andersson R. Effect of hyperoxia during the rest periods of interval training on perceptual recovery and oxygen re-saturation time. J Sports Sci. 2011;29:147–50.

    Article  PubMed  Google Scholar 

  25. White J, Dawson B, Landers G, et al. Effect of supplemental oxygen on post-exercise inflammatory response and oxidative stress. Eur J Appl Physiol. 2013;113:1059–67.

    Article  CAS  PubMed  Google Scholar 

  26. Maeda T, Yasukouchi A. Blood lactate disappearance during breathing hyperoxic gas after exercise in two different physical fitness groups-on the work load fixed at 70% VO2max. Appl Hum Sci. 1997;16:249–55.

    Article  CAS  Google Scholar 

  27. Kay B, Stannard SR, Morton RH, et al. Hyperoxia during recovery improves peak power during repeated wingate cycle performance. Braz J Biomotricity. 2008;2:92–100.

    Google Scholar 

  28. Sperlich B, Zinner C, Krueger M, et al. Effects of hyperoxia during recovery from 5 × 30-s bouts of maximal-intensity exercise. J Sports Sci. 2012;30:851–8.

    Article  PubMed  Google Scholar 

  29. Robbins MK, Gleeson K, Zwillich CW. Effect of oxygen breathing following submaximal and maximal exercise on recovery and performance. Med Sci Sports Exerc. 1992;24:720–5.

    Article  CAS  PubMed  Google Scholar 

  30. Grataloup O, Prieur F, Busso T, et al. Effect of hyperoxia on maximal O2 uptake in exercise-induced arterial hypoxaemic subjects. Eur J Appl Physiol. 2005;94:641–5.

    Article  CAS  PubMed  Google Scholar 

  31. Maeda T, Yasukouchi A. Blood lactate disappearance during breathing hyperoxic gas after exercise in two different physical fitness groups: on the workload fixed at 130% AT. Appl Hum Sci J Physiol Anthropol. 1998;17:33–40.

    Article  CAS  Google Scholar 

  32. Amann M. Significance of Group III and IV muscle afferents for the endurance exercising human. Clin Exp Pharmacol Physiol. 2012;39:831–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Perry CGR, Reid J, Perry W, et al. Effects of hyperoxic training on performance and cardiorespiratory response to exercise. Med Sci Sports Exerc. 2005;37:1175–9.

    Article  PubMed  Google Scholar 

  34. Perry CGR, Talanian JL, Heigenhauser GJF, et al. The effects of training in hyperoxia vs. normoxia on skeletal muscle enzyme activities and exercise performance. J Appl Physiol. (1985). 2007;102:1022–7.

    Article  CAS  Google Scholar 

  35. Armstrong WJ, Jacks DE, Sowash J, et al. The effect of training while breathing oxygen-enriched air on time-to-exhaustion and aerobic capacity. J Exerc Physiol. 2000;3:12–20.

    Google Scholar 

  36. Ploutz-Snyder LL, Simoneau JA, Gilders RM, et al. Cardiorespiratory and metabolic adaptations to hyperoxic training. Eur J Appl Physiol Occup Physiol. 1996;73:38–48.

    Article  CAS  PubMed  Google Scholar 

  37. Laursen PB, Francis GT, Abbiss CR, et al. Reliability of time-to-exhaustion versus time-trial running tests in runners. Med Sci Sports Exerc. 2007;39:1374–9.

    Article  PubMed  Google Scholar 

  38. Joyner MJ, Coyle EF. Endurance exercise performance: the physiology of champions. J Physiol. 2008;586:35–44.

    Article  CAS  PubMed  Google Scholar 

  39. Higgins J, Green S. Cochrane handbook for systematic reviews of interventions version 5.1.0 [updated March 2011]. The Cochrane Collaboration; 2011. www.handbook.cochrane.org.

  40. Thomas JR, French KE. The use of meta-analysis in exercise and sport: a tutorial. Res Q Exerc Sport. 1986;57:196–204.

    Article  Google Scholar 

  41. Ulrich S, Schneider SR, Bloch KE. Effect of hypoxia and hyperoxia on exercise performance in healthy individuals and in patients with pulmonary hypertension: a systematic review. J Appl Physiol. (1985). Epub 3 Aug 2017. doi:10.1152/japplphysiol.00186.2017.

  42. Moher D, Klassen TP, Schulz KF, et al. What contributions do languages other than English make on the results of meta-analyses? J Clin Epidemiol. 2000;53:964–72.

    Article  CAS  PubMed  Google Scholar 

  43. Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6:e1000100.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Cohen J. Statistical power analysis for the behavioral sciences. Hillsdale: Lawrence Earlbaum Associates; 1988. p. 20–6.

    Google Scholar 

  45. McLellan TM, Cheung SS, Jacobs I. Variability of time to exhaustion during submaximal exercise. Can J Appl Physiol. 1995;20:39–51.

    Article  CAS  PubMed  Google Scholar 

  46. Amann M, Hopkins WG, Marcora SM. Similar sensitivity of time to exhaustion and time-trial time to changes in endurance. Med Sci Sports Exerc. 2008;40:574–8.

    Article  PubMed  Google Scholar 

  47. Welch HG. Hyperoxia and human performance: a brief review. Med Sci Sports Exerc. 1982;14:253–62.

    Article  CAS  PubMed  Google Scholar 

  48. Byrnes WC, Mihevic PM, Freedson PS, et al. Submaximal exercise quantified as percent of normoxic and hyperoxic maximum oxygen uptakes. Med Sci Sports Exerc. 1984;16:572–7.

    CAS  PubMed  Google Scholar 

  49. Ulrich S, Hasler ED, Müller-Mottet S, et al. Mechanisms of improved exercise performance under hyperoxia. Respiration. 2017;93:90–8.

    Article  CAS  PubMed  Google Scholar 

  50. Bye PT, Esau SA, Walley KR, et al. Ventilatory muscles during exercise in air and oxygen in normal men. J Appl Physiol. 1985;1984(56):464–71.

    Google Scholar 

  51. Tucker R, Kayser B, Rae E, et al. Hyperoxia improves 20 km cycling time trial performance by increasing muscle activation levels while perceived exertion stays the same. Eur J Appl Physiol. 2007;101:771–81.

    Article  CAS  PubMed  Google Scholar 

  52. Peltonen JE, Rusko HK, Rantamäki J, et al. Effects of oxygen fraction in inspired air on force production and electromyogram activity during ergometer rowing. Eur J Appl Physiol. 1997;76:495–503.

    Article  CAS  Google Scholar 

  53. Hogan MC, Cox RH, Welch HG. Lactate accumulation during incremental exercise with varied inspired oxygen fractions. J Appl Physiol. 1985;1983(55):1134–40.

    Google Scholar 

  54. Marwood S, Bowtell J. No effect of glutamine supplementation and hyperoxia on oxidative metabolism and performance during high-intensity exercise. J Sports Sci. 2008;26:1081–90.

    Article  PubMed  Google Scholar 

  55. Linnarsson D, Karlsson J, Fagraeus L, et al. Muscle metabolites and oxygen deficit with exercise in hypoxia and hyperoxia. J Appl Physiol. 1985;1974(36):399–402.

    Google Scholar 

  56. Murray K, Sommerville A, McKenna M, et al. Normobaric hyperoxia training in elite female hockey players. J Sports Med Phys Fit. 2016;56(12):1488–93.

    Google Scholar 

  57. Wilson GD, Welch HG. Effects of hyperoxic gas mixtures on exercise tolerance in man. Med Sci Sports. 1975;7:48–52.

    CAS  PubMed  Google Scholar 

  58. Craig AD. How do you feel? Interoception: the sense of the physiological condition of the body. Nat Rev Neurosci. 2002;3:655–66.

    Article  CAS  PubMed  Google Scholar 

  59. Marcora S. Do we really need a central governor to explain brain regulation of exercise performance? Eur J Appl Physiol. 2008;104:929–31.

    Article  PubMed  Google Scholar 

  60. Gibson ASC, Baden DA, Lambert MI, et al. The conscious perception of the sensation of fatigue. Sports Med. 2003;33:167–76.

    Article  Google Scholar 

  61. Sperlich B, Zinner C, Krueger M, et al. Ergogenic effect of hyperoxic recovery in elite swimmers performing high-intensity intervals: hyperoxia and high-intensity exercise. Scand J Med Sci Sports. 2011;21:e421–9.

    Article  CAS  PubMed  Google Scholar 

  62. Peltonen JE, Rantamaki J, Niittymaki SP, et al. Effects of oxygen fraction in inspired air on rowing performance. Med Sci Sports Exerc. 1995;27:573–9.

    Article  CAS  PubMed  Google Scholar 

  63. Peltonen JE, Tikkanen HO, Ritola JJ, et al. Oxygen uptake response during maximal cycling in hyperoxia, normoxia and hypoxia. Aviat Space Env Med. 2001;72:904–11.

    CAS  Google Scholar 

  64. Petersen SR, Dreger RW, Williams BE, et al. The effects of hyperoxia on performance during simulated firefighting work. Ergonomics. 2000;43:210–22.

    Article  CAS  PubMed  Google Scholar 

  65. Volianitis S, Fabricius-Bjerre A, Overgaard A, et al. The cerebral metabolic ratio is not affected by oxygen availability during maximal exercise in humans. J Physiol. 2008;586:107–12.

    Article  CAS  PubMed  Google Scholar 

  66. Weltman A, Katch V, Sady S. Effects of increasing oxygen availability on bicycle ergometer endurance performance. Ergonomics. 1978;21:427–38.

    Article  CAS  PubMed  Google Scholar 

  67. Ekblom B, Huot R, Stein EM, et al. Effect of changes in arterial oxygen content on circulation and physical performance. J Appl Physiol. 1985;1975(39):71–5.

    Google Scholar 

  68. Linossier MT, Dormois D, Arsac L, et al. Effect of hyperoxia on aerobic and anaerobic performances and muscle metabolism during maximal cycling exercise. Acta Physiol Scand. 2000;168:403–12.

    Article  CAS  PubMed  Google Scholar 

  69. Manselin TA, Södergård O, Larsen FJ, et al. Aerobic efficiency is associated with the improvement in maximal power output during acute hyperoxia. Physiol Rep. 2017;5:e13119.

    Article  PubMed  PubMed Central  Google Scholar 

  70. Ohya T, Yamanaka R, Ohnuma H, et al. Hyperoxia extends time to exhaustion during high-intensity intermittent exercise: a randomized, crossover study in male cyclists. Sports Med Open. 2016;2:34.

    Article  PubMed  PubMed Central  Google Scholar 

  71. Plet J, Pedersen PK, Jensen FB, et al. Increased working capacity with hyperoxia in humans. Eur J Appl Physiol Occup Physiol. 1992;65:171–7.

    Article  CAS  PubMed  Google Scholar 

  72. Wilkerson DP, Berger NJA, Jones AM. Influence of hyperoxia on pulmonary O2 uptake kinetics following the onset of exercise in humans. Respir Physiol Neurobiol. 2006;153:92–106.

    Article  CAS  PubMed  Google Scholar 

  73. Eves ND, Petersen SR, Jones RL. The effect of hyperoxia on submaximal exercise with the self-contained breathing apparatus. Ergonomics. 2002;45:840–9.

    Article  PubMed  Google Scholar 

  74. Eves ND, Petersen SR, Jones RL. Effects of helium and 40% O2 on graded exercise with self-contained breathing apparatus. Can J Appl Physiol. 2003;28:910–26.

    Article  PubMed  Google Scholar 

  75. Hopman MTE, Folgering HTM, Groothuis JT, et al. The effect of inspired oxygen fraction on peak oxygen uptake during arm exercise. Eur J Appl Physiol. 2003;90:120–4.

    Article  CAS  PubMed  Google Scholar 

  76. Hughson RL, Kowalchuk JM. Kinetics of oxygen uptake for submaximal exercise in hyperoxia, normoxia, and hypoxia. Can J Appl Physiol. 1995;20:198–210.

    Article  CAS  PubMed  Google Scholar 

  77. Knight DR, Poole DC, Hogan MC, et al. Effect of inspired O2 concentration on leg lactate release during incremental exercise. J Appl Physiol. 1985;1996(81):246–51.

    Google Scholar 

  78. Lovering AT, Stickland MK, Amann M, et al. Hyperoxia prevents exercise-induced intrapulmonary arteriovenous shunt in healthy humans: hyperoxia prevents exercise-induced intrapulmonary shunt. J Physiol. 2008;586:4559–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Ozgurbuz C, Jung K, Teerfort N. Effects of oxygen application prior to exercise on performance and regeneration. Biol Sport. 2004;21:149–58.

    Google Scholar 

  80. Peltonen JE, Tikkanen HO, Rusko HK. Cardiorespiratory responses to exercise in acute hypoxia, hyperoxia and normoxia. Eur J Appl Physiol. 2001;85:82–8.

    Article  CAS  PubMed  Google Scholar 

  81. Prieur F, Benoit H, Busso T, et al. Effects of moderate hyperoxia on oxygen consumption during submaximal and maximal exercise. Eur J Appl Physiol. 2002;88:235–42.

    Article  CAS  PubMed  Google Scholar 

  82. Walsh ML, Banister EW. The influence of inspired oxygen on the oxygen uptake response to ramp exercise. Eur J Appl Physiol. 1995;72:71–5.

    Article  CAS  Google Scholar 

  83. Eiken O, Tesch PA. Effects of hyperoxia and hypoxia on dynamic and sustained static performance of the human quadriceps muscle. Acta Physiol Scand. 1984;122:629–33.

    Article  CAS  PubMed  Google Scholar 

  84. Kleiner DM, Snyder RC. The effectiveness of acute hyperoxia as an ergogenic aid for resistance exercise. J Strength Cond Res. 1995;9:228–31.

    Google Scholar 

  85. Mourtzakis M, González-Alonso J, Graham TE, et al. Hemodynamics and O2 uptake during maximal knee extensor exercise in untrained and trained human quadriceps muscle: effects of hyperoxia. J Appl Physiol. 1985;2004(97):1796–802.

    Google Scholar 

  86. Vanhatalo A, Fulford J, DiMenna FJ, et al. Influence of hyperoxia on muscle metabolic responses and the power-duration relationship during severe-intensity exercise in humans: a 31P magnetic resonance spectroscopy study. Exp Physiol. 2010;95:528–40.

    Article  CAS  PubMed  Google Scholar 

  87. Winter FD Jr, Snell PG, Stray-Gundersen J. Effects of 100% oxygen on performance of professional soccer players. JAMA. 1989;262:227–9.

    Article  PubMed  Google Scholar 

  88. Zinner C, Hauser A, Born DP, et al. Influence of hypoxic interval training and hyperoxic recovery on muscle activation and oxygenation in connection with double-poling exercise. PLoS ONE. 2015;10:1–12.

    Article  Google Scholar 

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Acknowledgements

The authors express their gratitude to Ms. Elizabeth Yates for her assistance with building the search strategy and to Dr. Christopher J. Tyler for advice on meta-analysis design and analysis.

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Correspondence to Stephen S. Cheung.

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Funding

Matthew M. Mallette is supported by a Queen Elizabeth II Ontario Graduate Scholarship in Science and Technology, Desmond G. Stewart is supported by a Natural Science and Engineering Research Council Undergraduate Summer Research Assistantship, and Stephen S. Cheung is supported by a Canada Research Chair. No other specific sources of funding were used to assist in the conduct of this meta-analysis or the preparation of this article.

Conflicts of Interest

Matthew Mallette, Desmond Stewart and Stephen Cheung declare that they have no conflicts of interest relevant to the content of this review.

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Mallette, M.M., Stewart, D.G. & Cheung, S.S. The Effects of Hyperoxia on Sea-Level Exercise Performance, Training, and Recovery: A Meta-Analysis. Sports Med 48, 153–175 (2018). https://doi.org/10.1007/s40279-017-0791-2

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