Next Article in Journal
Prices, Availability and Affordability of Medicines with Value-Added Tax Exemption: A Cross-Sectional Survey in the Philippines
Next Article in Special Issue
Hypoxic Pilates Intervention for Obesity: A Randomized Controlled Trial
Previous Article in Journal
Erratum: Therapeutic Atmosphere in Psychotherapy Sessions. Int. J. Environ. Res. Public Health 2020, 17, 4105
Previous Article in Special Issue
Impact of Active and Passive Hypoxia as Re-Warm-Up Activities on Rugby Players’ Performance

A Focused Review on the Maximal Exercise Responses in Hypo- and Normobaric Hypoxia: Divergent Oxygen Uptake and Ventilation Responses

Department of General and Surgical Intensive Care, Medical University Innsbruck, 6020 Innsbruck, Austria
Institute of Mountain Emergency Medicine, Eurac Research, 39100 Bolzano, Italy
Institute of Sport Sciences, Synathlon, Uni-Centre, 1015 Lausanne, Switzerland
Postoperative Critical Care Unit, Department of Anesthesiology and Critical Care Medicine, Medical University Innsbruck, 6020 Innsbruck, Austria
Department of Sport Science, University of Innsbruck, 6020 Innsbruck, Austria
Austrian Society for Alpine and Mountain Medicine, 6020 Innsbruck, Austria
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2020, 17(14), 5239;
Received: 14 May 2020 / Revised: 14 July 2020 / Accepted: 15 July 2020 / Published: 20 July 2020
(This article belongs to the Special Issue Hypoxia and Exercise: Effects on Health and Performance)


The literature suggests that acute hypobaric (HH) and normobaric (NH) hypoxia exposure elicits different physiological responses. Only limited information is available on whether maximal cardiorespiratory exercise test outcomes, performed on either the treadmill or the cycle ergometer, are affected differently by NH and HH. A focused literature review was performed to identify relevant studies reporting cardiorespiratory responses in well-trained male athletes (individuals with a maximal oxygen uptake, VO2max > 50 mL/min/kg at sea level) to cycling or treadmill running in simulated acute HH or NH. Twenty-one studies were selected. The exercise tests in these studies were performed in HH (n = 90) or NH (n = 151) conditions, on a bicycle ergometer (n = 178) or on a treadmill (n = 63). Altitudes (simulated and terrestrial) varied between 2182 and 5400 m. Analyses (based on weighted group means) revealed that the decline in VO2max per 1000 m gain in altitude was more pronounced in acute NH vs. HH (−7.0 ± 1.4% vs. −5.6 ± 0.9%). Maximal minute ventilation (VEmax) increased in acute HH but decreased in NH with increasing simulated altitude (+1.9 ± 0.9% vs. −1.4 ± 1.8% per 1000 m gain in altitude). Treadmill running in HH caused larger decreases in arterial oxygen saturation and heart rate than ergometer cycling in acute HH, which was not the case in NH. These results indicate distinct differences between maximal cardiorespiratory responses to cycling and treadmill running in acute NH or HH. Such differences should be considered when interpreting exercise test results and/or monitoring athletic training.
Keywords: exercise testing; normobaric; hypobaric; maximal oxygen uptake; maximal minute ventilation exercise testing; normobaric; hypobaric; maximal oxygen uptake; maximal minute ventilation

1. Introduction

When Mexico City (2300 m above sea level) was chosen to host the 1968 Olympic Games, sports scientists and coaches were challenged with performance limitations and physiological responses to exercise in acute hypobaric hypoxia (HH) [1,2,3]. Subsequently, there was a rise in scientific interest in evaluating the effects of acute normobaric hypoxia (NH) on exercise performance and on physiological responses [4,5]. Today, some 50 years later, comparisons between acute HH and NH still remain scarce [6,7,8]. It has to be noted that during the acclimatization process (with subacute and chronic exposures to altitude/hypoxia) physiological responses change associated with improved exercise performance [9,10].
A few years ago, Coppel and coworkers systematically reviewed the literature for physiological response differences between HH and NH [11]. This review and a more recent study [12] mainly focused on resting and submaximal exercise responses, with less emphasis on maximal exercise outcomes. Interestingly, most results indicated small differences in ventilatory parameters, however contrasting reports also exist [6,7,8]. Such divergent findings come as little surprise, as comparisons have often been affected by confounders such as the duration spent in hypoxia, temperature, and the humidity during exposure to hypoxia. Moreover, in some studies small sample sizes provide only limited statistical power [11,13,14].
With regard to potential exercise performance differences between HH and NH, the few existing comparative studies suggest a larger performance decline (e.g., time trial performance) in HH compared to NH [15]. Yet, little information is available on differences in physiological responses of athletes performing maximal exercise testing (i.e., incremental exercise test to exhaustion) in acute HH or NH.
Therefore, the aim of the present review was to summarize selected findings of studies investigating maximal incremental exercise test outcomes of well-trained athletes acutely exposed to HH (simulated and terrestrial) or NH.

2. Materials and Methods

A focused literature review was performed to identify relevant studies reporting cardiorespiratory responses of athletes performing cycling or treadmill running in acute HH or NH. The literature search was performed in the following databases using a cut-off date of May 2019: Pubmed/Medline, Web of Science, Science direct, Scopus, and Sport Discus. The following keywords were used: VO2max and acute hypoxia (or altitude) and athletes. Figure 1 displays a flow chart which depicts the selection process.
Inclusion criteria were well-trained male athletes (due to insufficient data on females), not exposed to altitudes above 2000 m for at least one month prior to the study, with a maximal oxygen consumption (VO2max ≥ 50 mL/min/kg) at sea level and studies reporting the outcomes of maximal incremental exercise tests (cycling or treadmill) completed at sea level and after acute exposure (ie., within the first 2 h, except one study where the ascent to real altitude lasted 8 h [9]) to HH (simulated and terrestrial) or NH at an altitude greater than 2000 m. Exercise test outcomes included VO2max, maximal minute ventilation (VEmax), peripheral oxygen saturation at maximal exercise (SpO2), and maximal heart rate (HRmax).


Data are presented as weighted group means and standard deviation (SD) of the mean. To allow for comparisons between different altitudes, changes in cardiorespiratory variables from sea level to altitude were calculated as deltas per 1000 m gain in altitude. The association between continuous variables was assessed using simple linear regression analyses. Potential differences of cardiorespiratory responses to HH or NH during cycling or treadmill running were evaluated by calculation of effect sizes (ES, Cohen’s d). An ES below 0.5 was considered to be small, 0.5 to 0.8 to be medium, and >0.8 to be large [16].

3. Results

A total of 21 studies were included, with 26 groups (n = 241 participants) evaluated at sea level and altitude (i.e., in NH or HH corresponding to altitude levels varying between 2182 and 5400 m). Out of 26 groups, 10 (n = 90) were performed in HH [9,17,18,19,20,21,22,23] (all in hypobaric chambers, except one which was performed at real altitude [9]), and 16 (n = 151) in NH [24,25,26,27,28,29,30,31,32,33,34]. Baseline characteristics of the groups included and the general physiological responses to maximal exercise testing at altitude are shown in Table 1.
Figure 2 depicts the salient findings of this focused review in regard to divergent oxygen uptake and ventilation responses in hypo- and normobaric hypoxia.
Effect sizes for differences between cycling and treadmill running could not be calculated because there was only one study evaluating treadmill running.
Table 2 displays the characteristics of the study participants of the studies included, separated by the HH and NH condition.
Table 3 depicts the differences between HH and NH per 1000 m of altitude gain separated by exercise task.
The data show that in NH, VO2max, combined for cycling and treadmill running, is reduced to a larger extent compared to HH (ES: 1.19). VEmax, combined for cycling and treadmill running, is slightly increased in HH, whereas it is reduced in NH (ES: 2.32); small to medium ES were detected for SpO2 (ES: 0.27) and HRmax (ES: 0.49) between conditions. Interestingly, when converting VEmax from body temperature pressure saturated (BTPS) to standard temperature pressure dry (STPD), VEmax values (STPD) were the same in NH and HH. Moderate to large effects were found between cycling and treadmill running in HH, indicating that VO2max (ES: 0.74), SpO2 (ES: 0.94) and HRmax (ES: 0.66) are more affected during treadmill running compared to cycling, although VEmax was slightly higher during treadmill running (ES: 0.35).
Furthermore, the data show a similar slope between changes in VO2max and SpO2max (Figure 3) and VEmax and HRmax (Figure 4) with gain in altitude, but at different levels for NH and HH.

4. Discussion

The main outcomes of the present literature review are that (for male athletes) the VO2max decline is larger in NH as compared to HH (simulated and terrestrial) and that VEmax slightly increases in HH whereas it is reduced in NH. Additionally, for each 1000 m of altitude gain in HH (simulated and terrestrial), VO2max during treadmill running seems to be more depressed compared to cycling. Furthermore, during treadmill running in HH (simulated and terrestrial), when compared to cycling, a larger SpO2max and HRmax decrease per 1000 m of altitude gain was found.
The VO2max reduction and the increase of VEmax at altitude are well documented [1,25,35,36,37]. It is also known that VO2max is reduced in both acute NH [25,27,28,29,30,32,33,34,38,39] and HH [9,17,18,19,20,21,22,23] conditions. Yet, information on specific VO2max differences between acute NH and HH in trained individuals is still lacking.
Previous work comparing differences between cardiorespiratory responses in acute HH and NH focused primarily on resting and submaximal exercise conditions [6,7,8,11,12,40]. Results of a recent meta-analysis (primarily performed on studies investigating resting conditions) indicate differences in variables related to VE, NO, fluid retention, and acute mountain sickness (AMS) associated factors between acute HH and NH [11]. The existence of such differences is also supported by Saugy et al. and Beidleman et al. who found differences in time trial performance between acute HH and NH, with greater performance losses during acute HH exposure [15,41]. In the study of Saugy et al. this was thought to be a result of a lower SpO2 in acute HH compared to NH, which was not reported by Beidleman et al. Both studies, however, did not determine cardiorespiratory responses at maximal exercise, which is of particular interest from an athletic training and testing perspective. To bridge this knowledge gap, the present analyses focused primarily on differences between acute NH and HH at maximal exercise. Larger VEmax responses in acute HH compared to NH (at comparable simulated altitude levels) may be expected due to the lower air density in HH [35]. Higher VEmax in acute HH compared to NH (during running) was recently demonstrated by Ogawa et al., which is likely due to a lower flow resistance in the airways [42]. When linking the reduced VEmax responses to the higher VO2max decline in NH compared to HH, the lower VEmax at reduced exercise performance has to be emphasized. This complicates the interpretation of VEmax changes when exercise is not performed at the same level of hypoxia in acute HH and NH. Distinct breathing patterns (i.e., tidal volume and breathing frequency) in acute HH and NH [43,44,45] might have influenced the central motor drive [46] and VO2max. Irrespective of these proposed mechanisms, it should be mentioned that Pugh demonstrated 50 years ago that exercise VE expressed as STPD remained unchanged at various altitudes at least up to 5800 m, while exercise VE expressed as BTPS (as is usually done) increased with the gain in altitude in a non-linear fashion [35]. Accordingly, similar VEmax values (STPD) in HH and NH were found when converting the VEmax values of the included studies from BTPS to STPD.
It is worth noting that a similar decrease of SpO2 at maximal exercise—despite different VEmax responses—was related to a more reduced VO2max in acute NH than in HH. Arterial oxygen desaturation has been shown to be linked to the decrease in HRmax. Decreases in HRmax, moreover might be influenced by the activity of the parasympathetic system or by myocardial electrophysiological and central factors [47,48,49]. Analyses of the results of the studies included revealed a similar relationship in acute NH (r2 = 0.8, p < 0.05) but not in HH. Whether this association is actually more important in acute NH than in HH has yet to be established. A higher SpO2 might be related to a higher performance level. Overall, it seems that there is a complex interplay between different respiratory, metabolic and autonomic regulations in NH and HH that might explain the observed differences in VO2max.
Beside the general responses of performing exercise in acute HH and NH, we found some small differences in the maximal cardiorespiratory responses between cycling and treadmill running. These differences are not straightforward to explain. Gavin and Stager demonstrated a more pronounced exercise-induced hypoxaemia (in normoxia) during cycling compared to running, potentially indicating a similar association in HH [50]. Generally, breathing patterns are different between cycling and running [51], potentially explaining the differences observed. Moreover, there is one excellent review specifically dealing with physiological differences between cycling and running [52]. Although differences will largely depend on the sport and training practiced, different responses to maximal exercise performed in normoxia, as outlined in that review [52], may help to explain such differences in hypoxia, as demonstrated in the present review. Millet and colleagues reported the following differences [52]. Whereas runners usually achieve higher VO2max values, in cyclists those values seem not to be different between cycling and treadmill running. Maximal heart rates have been found to be about 5% higher when derived from incremental treadmill running compared to cycling (at least in not well-trained individuals). Moreover, the delta efficiency was shown to be higher in running. Exercise ventilation is likely influenced by different pulmonary mechanics between cycling and treadmill running and may be more impaired in cycling than running. With regard to desaturation during maximal exercise, triathletes at least showed more pronounced desaturation (lower SpO2 values) during running than cycling.
In the present literature review, the focus was on maximal values during exercise testing. These results to some extent contrast those found during submaximal exercise. For instance, Netzer et al. found lower SpO2 and a higher HR values during exercise in HH compared to NH [53]. Similar to the present findings, Faiss et al. reported no differences in SpO2 values between conditions during cycling, yet VE was lower in acute HH compared to NH [45]. Similar to this, Beidleman et al. and Basualto-Alarcón et al. reported no effect of the type of condition on SpO2 and HR [6,15], yet exercise performance was more affected under acute HH conditions [15]. The differences in VE between submaximal and maximal exercise in acute NH and HH seem reasonable; the lower air density may allow a lower VE at submaximal exercise and a higher one at maximal exercise. With regard to exercise performance and SpO2, the factors discussed above (e.g., metabolic and autonomic regulation) may explain some of the differences, yet this has to be established in future studies.


Some limitations of the present analyses have to be acknowledged. First, we are aware that there have been a multitude of studies performing maximal incremental exercise testing in acute hypoxia. Yet, as the focus of those studies was on other topics, our literature search strategy might not have identified them. Nonetheless, the number of included studies and participants seems acceptable to allow the preliminary conclusions here presented. Second, analyses of data in this literature review have been performed on the basis of group averages, allowing effect sizes to be calculated. Third, we were not able to evaluate potential gender differences, as there are only very few studies including female athletes. Fourth, we must acknowledge that the validity of any comparison between acute NH and HH conditions depends on the accuracy of the calculation of the equivalent altitude, as was recently addressed in detail [40,54]. The calculation may depend on the location of the experimental site, the ambient temperature, or the degree of hygrometry and the official standard used [54]. In the present analysis, these factors were disregarded. Nonetheless, from a practical/real life perspective, our analysis seems valid, yet we urge others to perform studies designed to specifically address this issue (e.g., cross over studies with matched PiO2). In addition, available information does not allow whether participants were blinded in NH or not to be assessed with confidence. Thus, a potential placebo effect cannot be excluded. Finally, potential confounding may arise from the use of different test protocols and different measurement devices. Overall, this is the first review taking into account a reasonable number of studies evaluating cardiorespiratory exercise responses to maximal incremental exercise testing (treadmill and cycle ergometry) in trained individuals at sea level and in acute HH (simulated and terrestrial) and NH as well.

5. Conclusions

The analyses presented indicate that in well-trained men performing maximal exercise tasks, VO2max declines to a larger extent in acute NH compared to HH, which goes along a higher VEmax in HH. Treadmill running in acute HH caused more pronounced depressions of VO2max, SpO2, and HRmax compared to cycling exercise. These findings may have practical and clinical implications when interpreting exercise test results in acute NH and HH, and could inspire the design of according studies, but are also of novel applications in exercising in hypoxia.
Future studies will focus on potential sex and age differences between responses to acute NH and HH, but will also evaluate changes occurring with acclimatization.

Author Contributions

Conceptualization, M.B. and H.G.; methodology, M.B.; software, J.B.; validation, M.B., J.B., H.G., A.K. and B.T.; formal analysis, M.B. and J.B.; investigation, J.B.; resources, M.B.; data curation, M.B.; writing—original draft preparation, M.B., H.G., J.B., A.K. and B.T.; writing—review and editing, M.B., J.B., H.G., A.K. and B.T.; visualization, J.B.; supervision, M.B.; project administration, M.B.; All authors have read and agreed to the published version of the manuscript.


This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.


  1. Pugh, L.G. Athletes at altitude. J. Physiol. 1967, 192, 619–646. [Google Scholar] [CrossRef] [PubMed]
  2. Daniels, J.; Oldridge, N. The effects of alternate exposure to altitude and sea level on world-class middle-distance runners. Med. Sci. Sports 1970, 2, 107–112. [Google Scholar] [CrossRef] [PubMed]
  3. Mellerowicz, H.; Meller, W.; Wowerier, J.; Zerdick, J.; Ketusinh, O.; Kral, B.; Heepe, W. Comparative studies on the effect of high altitude training on permanent performance at lower altitudes. Schweiz. Z. Sportmed. 1971, (Suppl. 5–17). [Google Scholar] [PubMed]
  4. Hammond, M.D.; Gale, G.E.; Kapitan, K.S.; Ries, A.; Wagner, P.D. Pulmonary gas exchange in humans during normobaric hypoxic exercise. J. Appl. Physiol. 1986, 61, 1749–1757. [Google Scholar] [CrossRef] [PubMed]
  5. Schmidt, W.; Eckardt, K.U.; Hilgendorf, A.; Strauch, S.; Bauer, C. Effects of maximal and submaximal exercise under normoxic and hypoxic conditions on serum erythropoietin level. Int. J. Sports Med. 1991, 12, 457–461. [Google Scholar] [CrossRef] [PubMed]
  6. Basualto-Alarcón, C.; Rodas, G.; Galilea, P.A.; Riera, J.; Pagés, T.; Ricart, A.; Torrella, J.R.; Behn, C.; Viscor, G. Cardiorespiratory parameters during submaximal exercise under acute exposure to normobaric and hypobaric hypoxia. Apunts. Med. Esport 2012, 47, 65–72. [Google Scholar]
  7. Richard, N.A.; Sahota, I.S.; Widmer, N.; Ferguson, S.; Sheel, A.W.; Koehle, M.S. Acute mountain sickness, chemosensitivity, and cardiorespiratory responses in humans exposed to hypobaric and normobaric hypoxia. J. Appl. Physiol. 2014, 116, 945–952. [Google Scholar] [CrossRef]
  8. Woods, D.R.; O’Hara, J.P.; Boos, C.J.; Hodkinson, P.D.; Tsakirides, C.; Hill, N.E.; Jose, D.; Hawkins, A.; Phillipson, K.; Hazlerigg, A.; et al. Markers of physiological stress during exercise under conditions of normoxia, normobaric hypoxia, hypobaric hypoxia, and genuine high altitude. Eur. J. Appl. Physiol. 2017, 117, 893–900. [Google Scholar] [CrossRef]
  9. Horstman, D.; Weiskopf, R.; Jackson, R.E. Work capacity during 3-wk sojourn at 4300 m: Effects of relative polycythemia. J. Appl. Physiol. Respir. Environ. Exerc. Physiol. 1980, 49, 311–318. [Google Scholar] [PubMed]
  10. Burtscher, M.; Niedermeier, M.; Burtscher, J.; Pesta, D.; Suchy, J.; Strasser, B. Preparation for Endurance Competitions at Altitude: Physiological, Psychological, Dietary and Coaching Aspects. A Narrative Review. Front. Physiol. 2018, 9, 1504. [Google Scholar] [CrossRef]
  11. Coppel, J.; Hennis, P.; Gilbert-Kawai, E.; Grocott, M.P. The physiological effects of hypobaric hypoxia versus normobaric hypoxia: A systematic review of crossover trials. Extrem. Physiol. Med. 2015, 4, 2. [Google Scholar] [CrossRef] [PubMed]
  12. Boos, C.J.; O’Hara, J.P.; Mellor, A.; Hodkinson, P.D.; Tsakirides, C.; Reeve, N.; Gallagher, L.; Green, N.D.; Woods, D.R. A Four-Way Comparison of Cardiac Function with Normobaric Normoxia, Normobaric Hypoxia, Hypobaric Hypoxia and Genuine High Altitude. PLoS ONE 2016, 11, e0152868. [Google Scholar] [CrossRef] [PubMed]
  13. Viscor, G.; Torrella, J.R.; Corral, L.; Ricart, A.; Javierre, C.; Pages, T.; Ventura, J.L. Physiological and Biological Responses to Short-Term Intermittent Hypobaric Hypoxia Exposure: From Sports and Mountain Medicine to New Biomedical Applications. Front. Physiol. 2018, 9, 339. [Google Scholar] [CrossRef] [PubMed]
  14. Debevec, T.; Millet, G.P. Discerning normobaric and hypobaric hypoxia: Significance of exposure duration. J. Appl. Physiol. 2014, 116, 1255. [Google Scholar] [CrossRef]
  15. Beidleman, B.A.; Fulco, C.S.; Staab, J.E.; Andrew, S.P.; Muza, S.R. Cycling performance decrement is greater in hypobaric versus normobaric hypoxia. Extrem. Physiol. Med. 2014, 3, 8. [Google Scholar] [CrossRef]
  16. Cohen, J. Statistical Power Analysis for the Behavioral Sciences, 2nd ed.; Lawrence Erlbaum Associates: Hillsdale, NJ, USA, 1988. [Google Scholar]
  17. Beidleman, B.A.; Muza, S.R.; Rock, P.B.; Fulco, C.S.; Lyons, T.P.; Hoyt, R.W.; Cymerman, A. Exercise responses after altitude acclimatization are retained during reintroduction to altitude. Med. Sci. Sports Exerc. 1997, 29, 1588–1595. [Google Scholar] [CrossRef]
  18. Fagraeus, L.; Karlsson, J.; Linnarsson, D.; Saltin, B. Oxygen uptake during maximal work at lowered and raised ambient air pressures. Acta Physiol. Scand. 1973, 87, 411–421. [Google Scholar] [CrossRef]
  19. Fulco, C.S.; Rock, P.B.; Trad, L.; Forte, V.; Cymerman, A. Maximal cardiorespiratory responses to one- and two-legged cycling during acute and long-term exposure to 4300 meters altitude. Eur. J. Appl. Physiol. Occup. Physiol. 1988, 57, 761–766. [Google Scholar] [CrossRef]
  20. Koistinen, P.; Takala, T.; Martikkala, V.; Leppäluoto, J. Aerobic fitness influences the response of maximal oxygen uptake and lactate threshold in acute hypobaric hypoxia. Int. J. Sports Med. 1995, 16, 78–81. [Google Scholar] [CrossRef]
  21. Squires, R.W.; Buskirk, E.R. Aerobic capacity during acute exposure to simulated altitude, 914 to 2286 meters. Med. Sci. Sports Exerc. 1982, 14, 36–40. [Google Scholar] [CrossRef]
  22. Wehrlin, J.P.; Hallen, J. Linear decrease in VO2max and performance with increasing altitude in endurance athletes. Eur. J. Appl. Physiol. 2006, 96, 404–412. [Google Scholar] [CrossRef] [PubMed]
  23. Robergs, R.A.; Quintana, R.; Parker, D.L.; Frankel, C.C. Multiple variables explain the variability in the decrement in VO2max during acute hypobaric hypoxia. Med. Sci. Sports Exerc. 1998, 30, 869–879. [Google Scholar] [PubMed]
  24. Benoit, H.; Busso, T.; Castells, J.; Geyssant, A.; Denis, C. Decrease in peak heart rate with acute hypoxia in relation to sea level VO(2max). Eur. J. Appl. Physiol. 2003, 90, 514–519. [Google Scholar] [CrossRef] [PubMed]
  25. Ferretti, G.; Moia, C.; Thomet, J.M.; Kayser, B. The decrease of maximal oxygen consumption during hypoxia in man: A mirror image of the oxygen equilibrium curve. J. Physiol. 1997, 498, 231–237. [Google Scholar] [CrossRef] [PubMed]
  26. Friedmann, B.; Frese, F.; Menold, E.; Bärtsch, P. Effects of acute moderate hypoxia on anaerobic capacity in endurance-trained runners. Eur. J. Appl. Physiol. 2007, 101, 67–73. [Google Scholar] [CrossRef]
  27. Gavin, T.P.; Derchak, P.A.; Stager, J.M. Ventilation’s role in the decline in VO2max and SaO2 in acute hypoxic exercise. Med. Sci. Sports Exerc. 1998, 30, 195–199. [Google Scholar] [CrossRef]
  28. Heubert, R.A.; Quaresima, V.; Laffite, L.P.; Koralsztein, J.P.; Billat, V.L. Acute moderate hypoxia affects the oxygen desaturation and the performance but not the oxygen uptake response. Int. J. Sports Med. 2005, 26, 542–551. [Google Scholar] [CrossRef]
  29. Lawler, J.; Powers, S.K.; Thompson, D. Linear relationship between VO2max and VO2max decrement during exposure to acute hypoxia. J. Appl. Physiol. 1988, 64, 1486–1492. [Google Scholar] [CrossRef]
  30. Martin, D.; O’Kroy, J. Effects of acute hypoxia on the VO2 max of trained and untrained subjects. J. Sports Sci. 1993, 11, 37–42. [Google Scholar] [CrossRef]
  31. Mollard, P.; Woorons, X.; Letournel, M.; Lamberto, C.; Favret, F.; Pichon, A.; Beaudry, M.; Richalet, J.P. Determinants of maximal oxygen uptake in moderate acute hypoxia in endurance athletes. Eur. J. Appl. Physiol. 2007, 100, 663–673. [Google Scholar] [CrossRef]
  32. Ofner, M.; Wonisch, M.; Frei, M.; Tschakert, G.; Domej, W.; Kröpfl, J.M.; Hofmann, P. Influence of acute normobaric hypoxia on physiological variables and lactate turn point determination in trained men. J. Sports Sci. Med. 2014, 13, 774–781. [Google Scholar] [PubMed]
  33. Peltonen, J.E.; Tikkanen, H.O.; Ritola, J.J.; Ahotupa, M.; Rusko, H.K. Oxygen uptake response during maximal cycling in hyperoxia, normoxia and hypoxia. Aviat. Space Environ. Med. 2001, 72, 904–911. [Google Scholar] [PubMed]
  34. Robach, P.; Calbet, J.A.; Thomsen, J.J.; Boushel, R.; Mollard, P.; Rasmussen, P.; Lundby, C. The ergogenic effect of recombinant human erythropoietin on VO2max depends on the severity of arterial hypoxemia. PLoS ONE 2008, 3, e2996. [Google Scholar] [CrossRef] [PubMed]
  35. Pugh, L.G.C.E. Man at High Altitude. J. R. Coll. Physic. Lond. 1969, 3, 385–397. [Google Scholar]
  36. Lenfant, C.; Sullivan, K. Adaptation to high altitude. N. Engl. J. Med. 1971, 284, 1298–1309. [Google Scholar] [CrossRef]
  37. Cerretelli, P. Energy sources for muscular exercise. Int. J. Sports Med. 1992, 13 (Suppl. 1), S106–S110. [Google Scholar] [CrossRef]
  38. Friedmann, B. Training in hypoxia: Detrimental for muscular aerobic capacity? Acta Physiol. 2007, 190, 177. [Google Scholar] [CrossRef]
  39. Mollard, P.; Woorons, X.; Letournel, M.; Lamberto, C.; Favret, F.; Pichon, A.; Beaudry, M.; Richalet, J.P. Determinant factors of the decrease in aerobic performance in moderate acute hypoxia in women endurance athletes. Respir. Physiol. Neurobiol. 2007, 159, 178–186. [Google Scholar] [CrossRef]
  40. Millet, G.P.; Debevec, T. CrossTalk proposal: Barometric pressure, independent of PO2, is the forgotten parameter in altitude physiology and mountain medicine. J. Physiol. 2020, 598, 893–896. [Google Scholar] [CrossRef]
  41. Saugy, J.J.; Rupp, T.; Faiss, R.; Lamon, A.; Bourdillon, N.; Millet, G.P. Cycling Time Trial Is More Altered in Hypobaric than Normobaric Hypoxia. Med. Sci. Sports Exerc. 2016, 48, 680–688. [Google Scholar] [CrossRef]
  42. Ogawa, T.; Fujii, N.; Kurimoto, Y.; Nishiyasu, T. Effect of hypobaria on maximal ventilation, oxygen uptake, and exercise performance during running under hypobaric normoxic conditions. Physiol. Rep. 2019, 7, e14002. [Google Scholar] [CrossRef]
  43. Richard, N.A.; Koehle, M.S. Differences in cardio-ventilatory responses to hypobaric and normobaric hypoxia: A review. Aviat. Space Environ. Med. 2012, 83, 677–684. [Google Scholar] [CrossRef] [PubMed]
  44. Savourey, G.; Launay, J.C.; Besnard, Y.; Guinet, A.; Travers, S. Normo-and hypobaric hypoxia: Are there any physiological differences? Eur. J. Appl. Physiol. 2003, 89, 122–126. [Google Scholar] [CrossRef] [PubMed]
  45. Faiss, R.; Pialoux, V.; Sartori, C.; Faes, C.; Deriaz, O.; Millet, G.P. Ventilation, Oxidative Stress, and Nitric Oxide in Hypobaric versus Normobaric Hypoxia. Med. Sci. Sports Exerc. 2013, 45, 253–260. [Google Scholar] [CrossRef] [PubMed]
  46. Amann, M.; Dempsey, J.A. Ensemble Input of Group III/IV Muscle Afferents to CNS: A Limiting Factor of Central Motor Drive During Endurance Exercise from Normoxia to Moderate Hypoxia. Adv. Exp. Med. Biol. 2016, 903, 325–342. [Google Scholar] [PubMed]
  47. Mourot, L. Limitation of maximal heart rate in hypoxia: Mechanisms and clinical importance. Front. Physiol. 2018, 9, 972. [Google Scholar] [CrossRef] [PubMed]
  48. Mourot, L.; Millet, G.P. Is Maximal Heart Rate Decrease Similar Between Normobaric Versus Hypobaric Hypoxia in Trained and Untrained Subjects? High. Alt. Med. Biol. 2019, 20, 94–98. [Google Scholar] [CrossRef] [PubMed]
  49. Siebenmann, C.; Rasmussen, P.; Sorensen, H.; Bonne, T.C.; Zaar, M.; Aachmann-Andersen, N.J.; Nordsborg, N.B.; Secher, N.H.; Lundby, C. Hypoxia increases exercise heart rate despite combined inhibition of beta-adrenergic and muscarinic receptors. Am. J. Physiol. Heart Circ. Physiol. 2015, 308, H1540–H1546. [Google Scholar] [CrossRef]
  50. Gavin, T.P.; Stager, J.M. The effect of exercise modality on exercise-induced hypoxemia. Respir. Physiol. 1999, 115, 317–323. [Google Scholar] [CrossRef]
  51. Kalsås, K.; Thorsen, E. Breathing patterns during progressive incremental cycle and treadmill exercise are different. Clin. Physiol. Funct. Imaging 2009, 29, 335–338. [Google Scholar] [CrossRef]
  52. Millet, G.P.; Vleck, V.E.; Bentley, D.J. Physiological differences between cycling and running: Lessons from triathletes. Sports Med. 2009, 39, 179–206. [Google Scholar] [CrossRef] [PubMed]
  53. Netzer, N.C.; Rausch, L.; Eliasson, A.H.; Gatterer, H.; Friess, M.; Burtscher, M.; Pramsohler, S. SpO2 and Heart Rate During a Real Hike at Altitude Are Significantly Different than at Its Simulation in Normobaric Hypoxia. Front. Physiol. 2017, 8, 81. [Google Scholar] [CrossRef] [PubMed]
  54. Richalet, J.P. CrossTalk opposing view: Barometric pressure, independent of PO2, is not the forgotten parameter in altitude physiology and mountain medicine. J. Physiol. 2020, 598, 897–899. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flow chart of the protocol.
Figure 1. Flow chart of the protocol.
Ijerph 17 05239 g001
Figure 2. Schematic presentation of the key findings.
Figure 2. Schematic presentation of the key findings.
Ijerph 17 05239 g002
Figure 3. Relationship between changes (%) in peripheral oxygen saturation during maximal exercise (SpO2max) and maximal oxygen uptake (VO2max) per 1 km gain in altitude. Solid line (triangles) for hypobaric hypoxia (r2 = 0.40, p < 0.05) and dashed line (circles) for normobaric hypoxia (r2 = 0.39, p < 0.05). Delta values are calculated as HH/NH values minus sea level values.
Figure 3. Relationship between changes (%) in peripheral oxygen saturation during maximal exercise (SpO2max) and maximal oxygen uptake (VO2max) per 1 km gain in altitude. Solid line (triangles) for hypobaric hypoxia (r2 = 0.40, p < 0.05) and dashed line (circles) for normobaric hypoxia (r2 = 0.39, p < 0.05). Delta values are calculated as HH/NH values minus sea level values.
Ijerph 17 05239 g003
Figure 4. Relationship between changes (%) in maximal minute ventilation (VEmax) and maximal heart rates (HRmax) per 1 km gain in altitude. Solid line (triangles) for hypobaric hypoxia (r2 = 0.46, p < 0.05) and dashed line (circles) for normobaric hypoxia (r2 = 0.42, p < 0.05). Delta values are calculated as HH/NH values minus sea level values.
Figure 4. Relationship between changes (%) in maximal minute ventilation (VEmax) and maximal heart rates (HRmax) per 1 km gain in altitude. Solid line (triangles) for hypobaric hypoxia (r2 = 0.46, p < 0.05) and dashed line (circles) for normobaric hypoxia (r2 = 0.42, p < 0.05). Delta values are calculated as HH/NH values minus sea level values.
Ijerph 17 05239 g004
Table 1. Characteristics of the studies included in the analysis.
Table 1. Characteristics of the studies included in the analysis.
ReferenceParticipantsVO2max at Sea LevelAltitude or EquivalentHypoxia ConditionBaro-Metric PressureFiO2Exercise ModeVO2max at Altitude
(number)(mL/min/kg)(m) (mmHg)(%) (mL/min/kg)
Beidleman et al. (1997) [17]657.04300HH (HC)446 treadmill40.0
Benoit et al. (2003) [24]1264.25400NH 10.4cycling36.0
Benoit et al. (2003) [24]1750.85400NH 10.4cycling31.4
Fagraeus et al. (1973) [18]1150.13250HH (HC)520 cycling43.5
Ferretti et al. (1997) [25]562.12182NH 16.0cycling53.4
Ferretti et al. (1997) [25]562.14966NH 11.0cycling35.6
Friedmann et al. (2007) [26]2068.02682NH 15.0treadmill53.1
Fulco et al. (1988) [19]750.14300HH (HC)446 cycling37.2
Gavin et al. (1998) [27]760.43591NH 13.3cycling43.8
Gavin et al. (1998) [27]663.73591NH 13.3cycling42.1
Heubert et al. (2005) [28]962.72500NH 16.0cycling53.6
Horstman et al. (1980) [9]951.04300HH (TA)460 treadmill35.0
Koistinen et al. (1995) [20]1257.43200HH (HC)520 cycling46.6
Lawler et al. (1988) [29]765.03207NH 14.0cycling51.1
Martin et al. (1993) [30]867.23760NH 13.0cycling49.7
Mollard et al. (2007) [31]865.52479NH 15.4cycling57.7
Mollard et al. (2007) [31]865.54527NH 11.7cycling46.4
Ofner et al. (2014) [32]1051.03500NH 14.0cycling42.5
Peltonen et al. (2001) [33]661.82682NH 15.0cycling48.6
Robach et al. (2008) [34]750.02500NH 15.3cycling42.0
Robach et al. (2008) [34]750.03500NH 13.4cycling36.0
Robach et al. (2008) [34]750.04500NH 11.5cycling33.0
Robergs et al. (1998) [23]1460.42559HH (HC)566 cycling52.0
Squires et al. (1982) [21]1260.02286HH (HC)574 treadmill53.0
Wehrlin et al. (2006) [22]866.12300HH (HC)573 treadmill58.0
Wehrlin et al. (2006) [22]866.12800HH (HC)573 treadmill55.4
Maximal oxygen uptake, VO2max; fraction of inspired oxygen, FiO2; hypobaric hypoxia, HH (HC, hypobaric chamber; TA, terrestrial altitude); normobaric hypoxia, NH.
Table 2. Characteristics of study participants of the included HH and NH studies.
Table 2. Characteristics of study participants of the included HH and NH studies.
AllDivided by Exercise Mode
Hypobaric Hypoxia Studies
Variablen nCycling ExercisenTreadmill Running
Age (yr)9025.7 ± 3.74726.1 ± 4.34325.3 ± 3.0
Weight (kg)9073.6 ± 2.54773.5 ± 1.24373.7 ± 3.4
Height (cm)90178.8 ± 2.047178.1 ± 2.143179.5 ± 1.5
Altitude level (m)903117 ± 755473144 ± 577433087 ± 918
Normobaric Hypoxia Studies
Age (yr)14725.2 ± 3.412926.0 ± 2.91824.1 ± 4.1 *
Weight (kg)14772.6 ± 5.212972.9 ± 5.51871.2 ± 6.5
Height (cm)147178.7 ± 2.7129178.2 ± 2.518182.1 ± 5.9
Altitude level (m)1473678 ± 10951293830 ± 1099182682
Maximal oxygen uptake, VO2max; oxygen saturation, SpO2; maximal minute ventilation, VEmax; gas volumina are expressed as body temperature pressure saturated (BTPS). * Standard deviation (SD) taken from the respective study.
Table 3. Changes for each 1000 m altitude climb separately shown for altitude conditions and exercise mode.
Table 3. Changes for each 1000 m altitude climb separately shown for altitude conditions and exercise mode.
VariablenCycling + TreadmillnCycling + TreadmillnCycling ExercisenTreadmill RunningnCycling ExercisenTreadmill Running
∆VO2max (%/km)9
−5.6 ± 0.918
−7.0 ± 1.4 a4
−5.3 ± 0.75
−5.9 ± 0.9 b17
−6.8 ± 1.41
−8.1 ± 0.0
∆VEmax (%/km)9
1.9 ± 0.915
−1.4 ± 1.8 a4
1.8 ± 1.15
2.1 ± 0.5 c14
−1.6 ± 1.91
−0.2 ± 0.0
∆SpO2 (%/km)8
−4.6 ± 1.017
−5.0 ± 1.8 c3
−4.2 ± 0.95
−5.0 ± 0.8 a17
−5.0 ± 1.9//
∆HRmax (%/km)9
−1.6 ± 0.613
−2.1 ± 1.3 c4
−1.4 ± 0.75
−1.8 ± 0.5 b12
−2.0 ± 1.31
−3.0 ± 0.0
Heart rate, HR; hypobaric hypoxia, HH; maximal oxygen uptake, VO2max; normobaric hypoxia, NH; oxygen saturation, SpO2; ventilation, VE. Delta values are calculated as HH/NH values minus sea level values. n indicates the number of included studies (upper number) and the number of participants involved (lower number). a, b and c indicate large, medium, and small effect size respectively. ES for treadmill running in NH could not be calculated because only one study was available.
Back to TopTop