Skip to main content

Endurance-training in healthy men is associated with lesser exertional breathlessness that correlates with circulatory-muscular conditioning markers in a cross-sectional design


Whether exertional dyspnoea can be attributed to poor circulatory-muscular conditioning is a difficult clinical issue. Because criteria of poor conditioning such as low oxygen pulse, low ventilatory threshold or high heart rate/oxygen consumption slope can be observed in heart or lung diseases and are not specific to conditioning, we assessed the relationships between physical exercise, conditioning and exertional breathlessness in healthy subjects, in whom the aforementioned criteria can confidently be interpreted as reflecting conditioning.

To this end, healthy males with either low (inactive men, n = 31) or high (endurance-trained men, n = 31) physical activity evaluated using the International Physical Activity Questionnaire (IPAQ) underwent spirometry and incremental exercise testing with breathlessness assessment using Borg scale.

No significant breathlessness was reported before the ventilatory threshold in the two groups. Peak breathlessness was highly variable, did not differ between the two groups, was not related to any conditioning criterion, but correlated with peak respiratory rate. Nevertheless, endurance-trained subjects reported lower breathlessness at the same ventilation levels in comparison with inactive subjects. Significant but weak associations were observed between isoventilation breathlessness and physical activity indices (Borg at 60 L/min and total IPAQ scores, rho = -0.31, p = 0.020), which were mainly attributable to the vigorous domain of physical activity, as well as with conditioning indices (Borg score at 60 L.min-1 and peak oxygen pulse or heart rate/oxygen consumption slope, rho = -0.31, p = 0.021 and rho = 0.31, p = 0.020; respectively).

In conclusion, our data support a weak relationship between exertional breathlessness and circulatory-muscular conditioning, the later being primarily related to vigorous physical activity.


A common challenging issue in dyspnoea clinics is to determine whether dyspnoea can be attributed to reduced physical activity and subsequent poor circulatory-muscular conditioning in patients exhibiting normal or mildly altered exercise capacity, when cardio-pulmonary exercise testing fails to identify pathophysiological alterations consistent with respiratory or cardiovascular disease (Martinez et al.1994).

Mechanisms driving breathlessness induced by physical exercise are highly complex and include multiple determinants such as metabolic needs, ventilatory demand, ventilatory capacity, cardiovascular response, peripheral neural afferences including mecanoreceptors and chemoreceptors, and cortical integration of signals involving emotional cues (Burki and Lee2010). Interestingly, physical exercise itself holds an important place among therapeutical interventions known to reduce dyspnoea (breathlessness with negative affect) in patients with chronic heart or lung disease (Casaburi and ZuWallack2009; Downing and Balady2011), however the mechanisms of its effects deserve to be studied. In particular, whether better circulatory-muscular conditioning related to physical activity participates to a reduction in breathlessness/dyspnoea is unclear.

Conditioning comprises cardiac, microvascular and muscular adaptations which contribute to the optimization of oxygen delivery to exercising skeletal muscles. Markers of poor circulatory-muscular conditioning include slightly decreased peak oxygen consumption ( V O2), early onset of the ventilatory threshold, an increased heart rate/ V O2 (ΔHR/Δ V O2) relationship, and a reduction in oxygen pulse (American Thoracic Society and American College of Chest Physicians2003; Palange et al.2007). While determinants of conditioning are incompletely known, physical activity seems to play a major role, as improvements in the aforementioned criteria were demonstrated following exercise training over the whole range of human performance, from athletes undergoing intensive training to patients with severe obstructive lung disease (Laffite et al.2003; Ramponi et al.2013). While poor conditioning is commonly recognized as a possible cause of exercise intolerance or limitation (American Thoracic Society; American College of Chest Physicians2003; Martinez et al.1994; Palange et al.2007), its participation in breathlessness/dyspnoea, although suspected (Parshall et al.2012), deserves to be demonstrated. Data assessing relationships between conditioning/deconditioning criteria obtained from cardio-pulmonary exercise test and exertional breathlessness are scarce.

Criteria of poor conditioning such as low oxygen pulse, high ΔHR/Δ V O2 or low ventilatory threshold can be observed in heart or lung diseases and are thus not specific to conditioning, precluding the design of studies aiming at determining the impact of deconditioning on dyspnoea in diseased populations. For this reason, we chose to study the relationships between physical exercise, conditioning and exertional breathlessness in healthy subjects (without dyspnoea) with different levels of physical activity, in whom the aforementioned criteria could be confidently interpreted as reflecting conditioning. Consequently, indices of exertional breathlessness obtained from a cardiopulmonary exercise test (onset of breathlessness, isoventilation and iso V O2 comparisons, peak breathlessness) were compared in healthy men with either poor cardio-muscular conditioning (inactive) or good cardio-muscular conditioning (endurance-trained).



Healthy (no medication, never smokers or ex-smokers < 5 pack-year, no history of asthma) Caucasian men were recruited from the Clinical Investigation Center of Pompidou hospital and sport clubs. The study population sample comprised 32 inactive subjects (i.e. no regular sport practice, < 1 hour/week for five consecutive years), between 20 and 60 years of age, and 32 endurance-trained subjects (sport practice > 3 hours/week for 5 consecutive years), between 20 and 60 years of age (see Table 1). Physical inactivity was defined as not meeting specified American physical activity guidelines of at least 1 hour and 15 minutes a week of vigorous-intensity aerobic physical activity ( We used this definition because there is a lack of a clear and universal definition of a sedentary lifestyle (Varo et al.2003). One inactive man was unable to perform lung function testing and serial breathlessness assessment was unavailable in one trained subject. These two men were excluded. This was a cross-sectional study in which informed written consent was obtained from all subjects, and ethical approval (Comité de Protection des Personnes Ile De France VI, ID-RCB: 2011-A00006-35) was received. The subjects have previously been described as this investigation constituted an ancillary study of the SAINVAPU trial devoted to explore the physiology of pulmonary vascular recruitment/dilation on exercise (Al Dandachi et al.2014).

Table 1 Subject characteristics

Physical activity evaluation

Physical activity was evaluated using the French version of the International Physical Activity Questionnaire (IPAQ, long form) (Macfarlane et al.2006) administered by the physician in charge of the exercise test, before testing. IPAQ comprehensively assesses physical activity performed during leisure time physical activity, domestic and gardening activities, work-related physical activity, and transport-related physical activity (Craig et al.2003). The items in the long IPAQ form were structured to provide separate domain-specific scores for walking, moderate-intensity, and vigorous-intensity activity presented as median MET–minutes/week. The mean number of hours per week spent on sport practice was also recorded as a crude indicator of vigorous activity.

Spirometry and cardio-pulmonary exercise test

Spirometry was performed on MasterScreen systems (Jaeger, Carefusion, San Diego, USA), using reference values published by Quanjer and colleagues (Quanjer et al.1993). Symptom-limited incremental exercise testing was conducted on an electronically braked cycle ergometer using the Vmax Cardiopulmonary Exercise Testing System (Sensor Medics, Yorba Linda, CA) according to the recommended guidelines and reference values (American Thoracic Society; American College of Chest Physicians2003), as previously described (Delclaux et al.2011). After a 2 min warm-up period (inactive: 30 watts; trained subjects: 50 watts), the workload was increased by 15–30 Watts/minute, according to the degree of fitness, using a ramp protocol until exhaustion in order to obtain similar durations of exercise for the two groups of subjects. Ventilation and gas exchange measurements were performed breath-by-breath. Subjects rated the magnitude of their perceived breathing (breathlessness without negative affect) and leg discomfort at rest, every minute during exercise and at peak exercise by pointing to the 10-point Borg scale (Category scale with Ratio properties: CR10 (Borg and Kaijser2006), explained before testing); zero represented "no discomfort" and 10 represented "the most severe discomfort they could imagine experiencing". Slopes of Δ V O2/ΔWork rate, ΔHR/Δ V O2, Δ minute ventilation ( V E) /Δ V O2, Δ V E / Δ carbon dioxide production ( V CO2), and the anaerobic threshold (ventilatory threshold, using noninvasive determinations: ventilatory equivalents and V slope methods (American Thoracic Society; American College of Chest Physicians2003) were calculated. PaCO2 was monitored continuously using transcutaneous measurement at the ear (TOSCA 500, Radiometer, Copenhagen, Denmark), which allowed for the calculation of the physiological dead space/ tidal volume (VD/VT) ratio (corrected for valve dead space), as previously described (Delclaux et al.2011). Percentage of predicted peak minute ventilation was calculated as 100 × peak V E / 35 × forced expiratory volume in 1 second (FEV1).

Discomfort (leg, breathlessness) evaluation. In order to obtain an index characterising breathlessness during exercise related to ventilation available for all subjects, the Borg breathlessness score corresponding to 30% of predicted maximal ventilation was calculated. We also characterised the V O2 /breathlessness or V O2 /leg discombort relationships according to a power law: Breathlessness or leg discomfort = a × V O2b (Delclaux et al.2011).


Data are given as median, lower and upper quartiles. Comparisons between groups were performed using Mann-Whitney’s U-test. Univariate correlations were estimated using non parametric Spearman coefficients. Multivariate analyses were performed using multivariate regression (backward) after log-transformation of the variables. A p value < 0.05 was deemed significant. Statistical analyses were performed using Statview 5.0 software (SAS Institute, Inc, Cary, NC, USA). Due to the exploratory design of the study, no correction for multiplicity of testing was done (Rothman1990).


As shown in Table 1, inactive and endurance-trained subjects were well matched anthropomorphically. Similar peak heart rates were obtained in the two groups. The reasons for stopping the effort were similar in inactive and trained men (leg discomfort: 23 versus 21; breathlessness: 3 versus 6 and both: 5 versus 4; p = 0.587). The median IPAQ score of inactive and endurance-trained subjects was 1099 [695–2687] and 6966 [3865–10005] MET-min/week, respectively (Figure 1A). A close correlation between the number of hours spent on sport and the vigorous-activity domain of IPAQ was observed (Rho = 0.886, p < 0.001).

Figure 1
figure 1

Description of physical activity, conditioning markers and ventilatory demand in inactive and endurancetrained men. A] Total physical activity scores (total IPAQ, see Methods), B] Circulatory-muscular conditioning markers ( V O2 at ventilatory threshold (VT), heart rate (ΔHR) / Δ V O2 slope, peak oxygen pulse) and C] PaCO2 and ventilatory efficiency (Δ V E/Δ V O2 and Δ V E/Δ V CO2 slopes) markers in inactive (n = 31, white symbols) and endurance-trained (n = 31, grey symbols) men. Data are shown as medians, interquartile range, and extreme values. *p < 0.05.

As expected, endurance-trained subjects had better performance indices with higher peak work rate and peak V O2. Likewise, all indices of conditioning ( V O2 at ventilatory threshold, oxygen pulse, ΔHR/Δ V O2 slope) were significantly different in endurance-trained compared to inactive subjects, consistent with increasing circulatory-muscular conditioning in the former group (Figure 1B). Endurance-trained subjects had slightly increased PaCO2 in comparison with inactive subjects, both at rest and peak exercise, as well as better ventilatory efficiency as shown by decreased Δ V E/Δ V CO2 slope (Figure 1C). Physiological VD/VT ratio was very similar in both groups (0.34 [0.28-0.38] versus 0.34 [0.32-0.38], p = 0.472).

In both inactive and endurance-trained men, no significant breathlessness was reported before the ventilatory threshold (Borg score at ventilatory threshold: 0.5 [0–1] in inactive men, 0.5 [0–2] in endurance-trained men, p = 0.413). Peak breathlessness or perceived leg discomfort Borg scores did not differ between the two groups, and showed considerable variability (Table 1). Peak breathlessness was not related to performance (% predicted V O2) nor with any conditioning criterion. Among physiological parameters assessing ventilatory demand or response, peak breathlessness positively correlated with peak respiratory rate (rho = 0.301, p = 0.020).

Borg breathlessness scores were then compared at isoventilation levels. As shown in Figure 2A, endurance-trained subjects reported lower breathlessness at 60 and 80 L.min-1 of ventilation, in comparison with inactive subjects. Similarly, the perceived leg discomfort was reduced in the more active group at 40, 60, 80 and 100 L.min-1 (p < 0.001, p < 0.001, p = 0.002, p = 0.006, respectively).

Figure 2
figure 2

Relationships between breathlessness assessed by Borg scale and A] minute ventilation ( V E) expressed as absolute value and B] V O 2 expressed as a percentage of predicted value, in inactive men (n = 31, empty circles and dotted lines) and endurance-trained men (n = 31, filled squares and continuous lines). Upper panel. It gives the level of breathlessness (Borg score) according to the level of ventilation (20 to 100 L.min-1). Each point for a single patient is calculated by linear interpolation since the degree of breathlessness during the CPET is obtained according to time. All subjects did not reach V E at 60 L.min-1. Lower panel. Mean values of V O2 and Borg score (obtained by interpolation) are given every minute of the exercise test in the two groups of subjects. Data are shown for a minimum of n = 10 subjects at each V O2 point. Mean values and standard error of the mean are represented. *p < 0.05 between inactive and endurance-trained men.

The Borg breathlessness score corresponding to 30% of predicted maximal ventilation (see Table 1), characterizing the upper shift shown in Figure 2A, was logically significantly higher in inactive men as compared to trained men. Reduced breathlessness for similar exercise intensity in endurance-trained subjects was also readily apparent when breathlessness was plotted against V O2 (Figure 2B).

In line with these observations, the modelling of the V O2 /breathlessness relationship according to a power law showed a higher "a" constant in inactive men as compared to trained men (Table 1). Then, the exponent b was calculated for the V O2 /perceived leg discomfort relationship. The ratio of the exponents (b) was 0.95 ± 0.34 ( V O2 / breathlessness versus V O2 / leg discomfort), which was not significantly different from 1, suggesting similar shapes of increment on exercise of both breathlessness and leg discomfort.

Because both performance and conditioning indices showed overlap between inactive and endurance-trained subjects, data from the two groups were pooled to further explore relationships between activity levels, conditioning indices, and breathlessness. To determine whether conditioning indices were related to the level of physical activity, we explored the correlations between the total IPAQ score and its determinants on the one hand, and V O2 at Ventilatory Threshold, ΔHR/Δ V O2 slope and the oxygen pulse on the other hand, as well as age. As shown in Table 2 and Figure 3A, significant correlations were observed between all conditioning indices, peak V O2, and total physical activity. However, whereas moderate and vigorous physical activities were strongly associated with indices of circulatory/muscular conditioning, no association was observed between walking index and conditioning. Age and BMI were not associated with any conditioning index.

Table 2 Univariate spearman analysis of conditioning marker correlates
Figure 3
figure 3

Peak oxygen pulse expressed as percentage of predicted value, plotted against total physical activity score (IPAQ, see Methods), in inactive (n = 31, empty circles) and endurance-trained men (n = 31, filled circles).

Because endurance-trained subjects showed reduced exertional breathlessness in comparison to inactive subjects at isoventilation levels of 60 L.min-1 and 80 L.min-1, we then aimed to determine whether breathlessness at these ventilation levels (and also for normalized ventilation at 30% V E maximal predicted) was correlated with physical activity levels, conditioning indices, or ventilatory efficiency. As shown in Table 3, univariate correlation analyses showed significant associations between breathlessness at isoventilation levels and physical activity (Figure 4A), which were mainly attributable to the vigorous domain of physical activity. Significant associations were also found between exertional breathlessness and indices of cardio-muscular conditioning (Figure 4B). By contrast, ventilatory efficiency/demand (Δ V E/Δ V CO2 slope) was not associated with these breathlessness criteria in this cohort of subjects free of any lung or heart disease. Age was not associated with any breathlessness index.

Table 3 Relationships between breathlessness indices and conditioning or ventilatory demand
Figure 4
figure 4

Breathlessness at 60 L.min -1 ventilation plotted against A] total physical activity score (IPAQ score, see Methods) and B] heart rate (ΔHR)/ Δ V O 2 , in inactive (n = 31, empty circles) and endurance-trained men (n = 31, filled circles).

The association of breathlessness at isoventilation levels with parameters related to physical activity and cardio-circulatory conditioning was then tested using multivariate analyses. These analyses confirmed that physical activity and conditioning indices were not independent determinants of breathlessness.


The main results of this cross-sectional physiological study are that 1) the onset of breathlessness began concomitantly with a conditioning criterion (ventilatory threshold), 2) breathlessness and perceived leg discomfort had similar shapes of increment on exertion, and 3) trained subjects experienced less breathlessness for similar levels of ventilation than inactive men, which was associated with the degree of conditioning. The three results suggest a weak but significant link between circulatory-muscular conditioning and exertional breathlessness, at least in healthy men.

The link between peak V O2 and physical activity in our study is in line with previous studies showing significant relationships between leisure time physical activities and aerobic capacity in healthy subjects, where such associations were mostly driven by high-intensity activities and independent of age (Loe et al.2013; Talbot et al.2000). Our observation of correlations between physical activity on the one hand, and ΔHR/Δ V O2, oxygen pulse and the ventilatory threshold on the other hand, support the hypothesis that such parameters may be considered physiological markers of circulatory-muscular conditioning as suggested by ATS guidelines (American Thoracic Society; American College of Chest Physicians2003). However, although relationships between physical activity and conditioning markers were statistically significant in our study, Rho values indicated mostly moderate relationships, in agreement with previous studies where V O2-activity relationships were weak (Loe et al.2013). This finding is consistent with the fact that peak V O2 and peak oxygen pulse are firmly related to genetic hereditary, as was demonstrated in studies in siblings and in dizygotic and monozygotic twins, where genetic factors accounted for 40% of variance in peak V O2 and 60% of variance in oxygen pulse (Bouchard et al.1986).

In addition to increased peak V O2 and markers of circulatory-muscular conditioning, endurance-trained men showed a decreased Δ V E/Δ V CO2 slope (ventilatory demand) in comparison with inactive men indicating better ventilatory efficiency, consistent with a beneficial effect of training regarding V E/ V CO2 (Yerg et al.1985). Because physiological dead space measurements were very similar in both groups, this increase in ventilatory efficiency can be attributed to the relative alveolar hypoventilation observed in endurance-trained subjects. This result raises the hypothesis that elevation of the PaCO2 set-point may be a usual adaptation to endurance training. The mechanisms by which training may alter the PaCO2 set-point are unclear, as no difference in CO2 chemosensitivity has been found between endurance-trained athletes and control subjects (McConnell and Semple1996). Since PaCO2 did not correlate with physical activity levels, whether hypoventilation was related to training or to selection bias cannot be inferred from our results.

Our data support a relationship between endurance training, circulatory-muscular conditioning and exertional breathlessness. Firstly, breathlessness began at the ventilatory threshold, which is tightly related to conditioning. Secondly, breathlessness and perceived leg discomfort muscular fatigue developed in a similar way (similar b exponents), and thirdly trained subjects showed reduced breathlessness at similar levels of ventilation in comparison with inactive subjects with significant correlations between isoventilation breathlessness, physical activities and conditioning indices. Decreased breathlessness at isoventilation in trained subjects could be related to better conditioning of respiratory muscles (greater inspiratory muscle strength), higher ventilatory capacity and/or desensitization to the stimulus. The perceived leg discomfort/fatigue was similarly reduced in the more active group suggesting greater global skeletal muscle strength or desensitization. In support of the former hypothesis, Hamilton and colleagues showed a relationship between power output measured during an exercise test and dyspnoea, according to the strength of inspiratory muscles (Hamilton et al.1995). In support of the latter, physical activity, as performed in the setting of rehabilitation programs, has been shown to decrease exertional dyspnoea in patients with heart or respiratory diseases, even in the absence of a benefit in terms of performance (Casaburi and ZuWallack2009), while repetition of exercise tests in patients with obstructive lung disease has also been associated with short-term reduction in breathlessness (Belman et al.1991).

Despite a correlation between breathlessness and respiratory rate at peak exercise, our results show a partial disconnect between breathlessness and respiratory effort, in line with concepts linking exertional breathlessness or dyspnoea to multiple determinants beyond an increased work of breathing (Burki and Lee2010). Whether altered PaCO2 set-point or CO2 chemosensitivity contributed to reduced exertional breathlessness in trained subjects, or vice versa, could not be evidenced in this study.

Our study has inherent limitations due to its cross-sectional design. Statistical differences and correlations did not demonstrate causality. Reporting bias may be suspected as physical activity levels were measured using questionnaires (Macfarlane et al.2006), whereas over-reporting of physical activity in males has been described (Klesges et al.1990). Nevertheless, IPAQ long form has been recommended for research requiring more detailed assessment (Craig et al.2003). As only men were included, results may not be valid in women. All subjects were healthy and did not report dyspnoea, defined by a negative affect associated with breathlessness, mandating caution before extrapolation of our results to diseased populations. Finally, because vigorous exercise was inherently rare in inactive patients, selection bias may have led to overestimation of its weight relative to moderate exercise or walking.

From a clinical perspective, our results raise two important issues. First, in what measure can excessive exertional breathlessness be attributed to poor conditioning in an inactive or sedentary patient with a complaint of dyspnoea? Since statistical relationships between isoventilation breathlessness and conditioning criteria were weak (~10% of breathlessness variance), and due to the multiplicity of determinants of physiological breathlessness, in clinical practice it may be very difficult to confidently attribute dyspnoea to circulatory-muscular deconditioning in otherwise healthy subjects, a diagnosis that may be overestimated.

Second, in these results obtained in healthy men, and in agreement with a previous study (Talbot et al.2000), walking or moderate physical activity played a minor role in comparison with vigorous physical activity in terms of increased circulatory-muscular conditioning and reduced exertional breathlessness, raising the question whether rehabilitation programs offered to patients with heart or respiratory failure may be improved by a focus on high-intensity, high breathlessness exercise as suggested by the recent demonstrations of superiority of nonlinear or interval exercise training in patients with chronic obstructive pulmonary disease or heart failure (Haykowsky et al.2013; Klijn et al.2013).

In conclusion, cardio-muscular conditioning indices and an index of exertional breathlessness are linked to a weak extent in healthy men. As a consequence, in otherwise healthy patients it may be difficult to ascribe dyspnoea to circulatory-muscular deconditioning.


( V O2):

oxygen consumption

(ΔHR/Δ V O2):

heart rate/ V O2 relationship/slope


International Physical Activity Questionnaire

( V E):

Minute ventilation

( V CO2):

Carbon dioxide production


dead space/tidal volume


forced expiratory volume in 1 second


body mass index


  • Al Dandachi G, Londner C, Caumont-Prim A, Plantier L, Chevalier-Bidaud B, Toussaint JF, Desgorces FD, Delclaux C: Ageing and endurance training effects on quantity and quality of pulmonary vascular bed in healthy men. Respir Res 2014, 15: 8.

    Article  Google Scholar 

  • American Thoracic Society; American College of Chest Physicians: ATS/ACCP Statement on cardiopulmonary exercise testing. Am J Respir Crit Care Med 2003, 167(2):211-277.

    Article  Google Scholar 

  • Belman MJ, Brooks LR, Ross DJ, Mohsenifar Z: Variability of breathlessness measurement in patients with chronic obstructive pulmonary disease. Chest 1991, 99(3):566-571.

    Article  Google Scholar 

  • Borg E, Kaijser L: A comparison between three rating scales for perceived exertion and two different work tests. Scand J Med Sci Sports 2006, 16(1):57-69.

    Article  Google Scholar 

  • Bouchard C, Lesage R, Lortie G, Simoneau JA, Hamel P, Boulay MR, Perusse L, Theriault G, Leblanc C: Aerobic performance in brothers, dizygotic and monozygotic twins. Med Sci Sports Exerc 1986, 18(6):639-646.

    Article  Google Scholar 

  • Burki NK, Lee LY: Mechanisms of dyspnea. Chest 2010, 138(5):1196-1201.

    Article  Google Scholar 

  • Casaburi R, ZuWallack R: Pulmonary rehabilitation for management of chronic obstructive pulmonary disease. N Engl J Med 2009, 360(13):1329-1335.

    Article  Google Scholar 

  • Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P: International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc 2003, 35(8):1381-1395.

    Article  Google Scholar 

  • Delclaux C, Chevalier-Bidaud B, Essalhi M, Callens E, Graba S, Gillet-Juvin K, Valcke-Brossollet J, Mahut B: Too rapid increase and too much breathlessness are distinct indices of exertional dyspnea in COPD. Respir Physiol Neurobiol 2011, 176(1–2):32-38.

    Article  Google Scholar 

  • Downing J, Balady GJ: The role of exercise training in heart failure. J Am Coll Cardiol 2011, 58(6):561-569.

    Article  Google Scholar 

  • Hamilton AL, Killian KJ, Summers E, Jones NL: Muscle strength, symptom intensity, and exercise capacity in patients with cardiorespiratory disorders. Am J Respir Crit Care Med 1995, 152(6 Pt 1):2021-2031.

    Article  Google Scholar 

  • Haykowsky MJ, Timmons MP, Kruger C, McNeely M, Taylor DA, Clark AM: Meta-analysis of aerobic interval training on exercise capacity and systolic function in patients with heart failure and reduced ejection fractions. Am J Cardiol 2013, 111(10):1466-1469.

    Article  Google Scholar 

  • Klesges RC, Eck LH, Mellon MW, Fulliton W, Somes GW, Hanson CL: The accuracy of self-reports of physical activity. Med Sci Sports Exerc 1990, 22(5):690-697.

    Article  Google Scholar 

  • Klijn P, van Keimpema A, Legemaat M, Gosselink R, van Stel H: Nonlinear exercise training in advanced chronic obstructive pulmonary disease is superior to traditional exercise training. A randomized trial. Am J Respir Crit Care Med 2013, 188(2):193-200.

    Article  Google Scholar 

  • Laffite LP, Mille-Hamard L, Koralsztein JP, Billat VL: The effects of interval training on oxygen pulse and performance in supra-threshold runs. Arch Physiol Biochem 2003, 111(3):202-210.

    Article  Google Scholar 

  • Loe H, Rognmo O, Saltin B, Wisloff U: Aerobic capacity reference data in 3816 healthy men and women 20–90 years. PLoS One 2013, 8(5):e64319.

    Article  Google Scholar 

  • Macfarlane DJ, Lee CC, Ho EY, Chan KL, Chan D: Convergent validity of six methods to assess physical activity in daily life. J Appl Physiol 2006, 101(5):1328-1334.

    Article  Google Scholar 

  • Martinez FJ, Stanopoulos I, Acero R, Becker FS, Pickering R, Beamis JF: Graded comprehensive cardiopulmonary exercise testing in the evaluation of dyspnea unexplained by routine evaluation. Chest 1994, 105(1):168-174.

    Article  Google Scholar 

  • McConnell AK, Semple ES: Ventilatory sensitivity to carbon dioxide: the influence of exercise and athleticism. Med Sci Sports Exerc 1996, 28(6):685-691.

    Article  Google Scholar 

  • Palange P, Ward SA, Carlsen KH, Casaburi R, Gallagher CG, Gosselink R, O'Donnell DE, Puente-Maestu L, Schols AM, Singh S, Whipp BJ: Recommendations on the use of exercise testing in clinical practice. Eur Respir J 2007, 29(1):185-209.

    Article  Google Scholar 

  • Parshall MB, Schwartzstein RM, Adams L, Banzett RB, Manning HL, Bourbeau J, Calverley PM, Gift AG, Harver A, Lareau SC, Mahler DA, Meek PM, O’Donnell DE: An official American thoracic society statement: update on the mechanisms, assessment, and management of dyspnea. Am J Respir Crit Care Med 2012, 185(4):435-452.

    Article  Google Scholar 

  • Quanjer PH, Tammeling GJ, Cotes JE, Pedersen OF, Peslin R, Yernault JC: Lung volumes and forced ventilatory flows. Report working party standardization of lung function tests, European community for steel and coal. Official statement of the European respiratory society. Eur Respir J Suppl 1993, 16: 5-40.

    Article  Google Scholar 

  • Ramponi S, Tzani P, Aiello M, Marangio E, Clini E, Chetta A: Pulmonary rehabilitation improves cardiovascular response to exercise in COPD. Respiration 2013, 86(1):17-24.

    Article  Google Scholar 

  • Rothman KJ: No adjustments are needed for multiple comparisons. Epidemiology 1990, 1(1):43-46.

    Article  Google Scholar 

  • Talbot LA, Metter EJ, Fleg JL: Leisure-time physical activities and their relationship to cardiorespiratory fitness in healthy men and women 18–95 years old. Med Sci Sports Exerc 2000, 32(2):417-425.

    Article  Google Scholar 

  • Varo JJ, Martinez-Gonzalez MA, De Irala-Estevez J, Kearney J, Gibney M, Martinez JA: Distribution and determinants of sedentary lifestyles in the European Union. Int J Epidemiol 2003, 32(1):138-146.

    Article  Google Scholar 

  • Yerg JE 2nd, Seals DR, Hagberg JM, Holloszy JO: Effect of endurance exercise training on ventilatory function in older individuals. J Appl Physiol 1985, 58(3):791-794.

    Google Scholar 

Download references


The authors wish to thank the technicians of the pulmonary function laboratory for their expert assistance (Martine Riquelme, Françoise Genisty, Mireille Morot, Marien Bokouabassa), the different contributors from the Unité de Recherche Clinique of the Hôpital Européen Georges Pompidou (Gilles Chatellier [medical coordinator], Noël Lucas [medical coordinator], Yann Guivarch [financial account manager], Chantal Andrieux [clinical trial coordinator] and Kévin Masini [data manager]), the Centre d’Investigations Cliniques (recruitment of healthy subjects, Dr. Anne Blanchard and Prof Michel Azizi, director) and the Direction de la Recherche Clinique et du Développement (DRCD of AP-HP: Damien Vanhoye) for sponsoring.

Christophe Delclaux takes responsibility for the content of the manuscript.


This study was funded by a grant from the Assistance Publique - Hôpitaux de Paris (AP-HP : Direction de la Recherche Clinique et du Développement). The Unité de Recherche Clinique was responsible for independent data monitoring and analysis (Aurore Caumont-Prim) under the supervision of our sponsor (Assistance Publique – Hôpitaux de Paris; project code: P101102, SAINVAPU study). The sponsor had no role in study design, in the collection, analysis and interpretation of data, in the writing of the report and in the decision to submit the article for publication.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Laurent Plantier.

Additional information

Competing interests

All the authors declare no competing interests.

Authors’ contributions

All the authors made substantial contributions to conception and design (LP, JFT, FDD, CD2), or acquisition of data (GAD, CL, LP, BCB), or analysis and interpretation of data (ACP); drafted the submitted article or revised it critically for important intellectual content (all authors); and provided final approval of the version to be published (all authors).

Authors’ original submitted files for images

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Plantier, L., Al Dandachi, G., Londner, C. et al. Endurance-training in healthy men is associated with lesser exertional breathlessness that correlates with circulatory-muscular conditioning markers in a cross-sectional design. SpringerPlus 3, 426 (2014).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: