Abstract
It has recently been demonstrated that in healthy individuals, peak oxygen consumption is associated with a greater pulmonary capillary blood volume and a more distensible pulmonary circulation. Our cross-sectional study suggests that, in healthy men aged 20 to 60 years (n = 63), endurance sport practice (vigorous-intensity domain of the International Physical Activity Questionnaire) is associated with better quantity (pulmonary capillary blood volume) and quality (slope of increase in lung diffusion for carbon monoxide on exercise) of the pulmonary vascular bed, partly counterbalancing the deleterious effects of ageing, which remains to be demonstrated in a prospective longitudinal design.
Findings
Background
Pulmonary vascular response to exercise varies considerably from one individual to another [1], which is partly explained by the natural distensibility of the pulmonary circulation [2]. Capillary resistance significantly contributes to changes in pulmonary vascular resistance during exercise. Capillary blood volume available for gas exchange (VC) can be estimated from lung diffusing capacity measurements using both carbon monoxide (CO) and nitric oxide (NO) as tracer gases [3]. Lalande et al. recently demonstrated that in healthy individuals, peak oxygen consumption () on exercise is associated with a greater pulmonary capillary blood volume and a more distensible pulmonary circulation [4], which is in keeping with the notion that a greater pulmonary vascular reserve allows for a higher aerobic exercise capacity, and vice-versa. On the opposite, ageing is associated with a progressive deterioration of the structure and function of the pulmonary vascular bed [5, 6]. Using normative equations, one can calculate that VC would be zero around 100 years [7].
Methods
We thus enrolled both inactive and active (endurance-trained) healthy men to evaluate whether physical activity and age were correlated with VC at rest and with the increase in lung diffusion of CO (DLCO) on exercise. Physical activity was evaluated using the French version of the International Physical Activity Questionnaire (IPAQ, long form) [8] that evaluates vigorous, moderate and walking activity domains. The resting VC was calculated using DLCO and lung diffusion of NO (DLNO) measured simultaneously by the single-breath technique (4 seconds breath-hold, corrected for haemoglobin, assuming negligible erythrocyte resistance to NO [9], using an automatic apparatus (MasterScreenBody, Jaeger), as previously described [10]). VC measurements were also obtained at two levels of exercise (warm-up period and at 50% of the maximal work rate: see Figure 1, experimental protocol) to calculate the slope of the DLCO/work relationship as an index evaluating the dynamic capillary blood volume recruitment/dilation on exercise. The linearity of the relationship between power and DLCO has been demonstrated for ≤60% of [11]. Symptom-limited incremental exercise testing was conducted on an electronically braked cycle ergometer according to the recommended guidelines [12], as previously described [13] using a 2 min warm-up period followed by a ramp protocol (see Figure 1 legend) until exhaustion. Spirometry was obtained before exercise.
Description of the investigations (experimental protocol). 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). After a 2 min warm-up period (inactive: 30 watts; trained subjects: 50 watts, corresponding to ~15% of ), the workload was increased by 15–30 Watts/minute using a ramp protocol until exhaustion. The single breath DLCO/DLNO measurements were obtained at rest and at two levels of exercise (a first warm-up period was performed before the ramp exercise test, and at 50% of the maximal work rate, immediately after peak exercise acquisition).
Results
A total of 64 healthy (no medication, never smokers or ex-smokers <5 pack-year, no history of asthma, between 40 and 60 years of age) Caucasian men were recruited: 32 inactive subjects (not meeting specified American physical activity guidelines of at least 1 hour and 15 minutes a week of vigorous-intensity aerobic physical activity, for five consecutive years) and 32 endurance-trained subjects (sport practice >3 hours/week for 5 consecutive years). One inactive man was unable to perform apneas for DLCO measurements and was excluded. Informed written consent was obtained from all subjects, and ethical approval (CPP IDF VI, ID-RCB: 2011-A00006-35) was received.
The main characteristics of the healthy men at rest and on exercise are described in Table 1 while univariate analyses of factors associated with the quantity and quality indices of pulmonary vascular bed are described in Table 2 and Figure 2. Multivariate analyses (age, height and activity as independent variables) demonstrated that both age and vigorous-intensity activity domain remained independent predictors of resting VC (R2 = 0.37, p-value (vigorous intensity activity) = 0.0123, p-value (age) <0.001), and of the slope of DLCO increase (R2 = 0.25).
Factors associated with resting capillary blood volume. The panel A describes the relationship between age (years) and resting capillary blood volume available for gas exchange (VC, mL) in inactive (closed circles) and endurance-trained (open circles) men. A significant relationship is evidenced (see Table 2). The panel B describes the relationship between the vigorous-intensity activity domain of the International Physical Activity Questionnaire (Vigorous-IPAQ) and resting VC. A significant relationship is evidenced (see Table 2). The panel C describes the relationship between resting VC and expressed as raw values, while the panel D describes the relationship between normalized for age and height (expressed as% predicted, see Table fourteen in [12]). The statistical significance of the relationship of panel C is given in Table 2. The significance of the relationship of panel D (r = 0.311, p = 0.013) further suggests that VC is an independent (of age and height) predictor of .
Discussion
Lalande et al. recently demonstrated that is associated with a greater VC and with a more distensible pulmonary circulation [4] that deserved to be confirmed. We enrolled a larger sample of healthy subjects with a wide range of physical activity levels allowing to establish the relationship between physical activity and and to perform a multivariate analysis more confidently. Different methods for VC measurement have been used with and without inhaled NO; their agreement is satisfactory [14]. The degree of both DLCO and VC increase during exercise (~20-25%) in our study was similar with that described by Lalande et al. [4]. Overall, the level of statistical significance of the correlations evidenced is weak to moderate. Several factors may explain this finding such as genetic heritability and inherent limitations due to indirect measures of vascular indices (with two outliers, see Figure 1). The genetic heritability of is around 50% [15], which may explain the overlap between is evidenced in inactive and trained men in our study, and further justify the weak relationship between physical activity and vascular indices.
The results of this cross-sectional study rely on correlations that do not make causality. Nevertheless, one may hypothesize that endurance sport practice favours lung growth and capillary blood volume increase as observed for lung volumes [16, 17].
In conclusion, our cross-sectional study suggests that, in healthy men aged 20 to 60 years, endurance sport practice is associated with better quantity and quality of the pulmonary vascular bed, partly counterbalancing the deleterious effects of ageing, which remains to be demonstrated in a prospective longitudinal design.
Abbreviations
- VC:
-
capillary blood volume available for gas exchange
- CO:
-
carbon monoxide
- NO:
-
nitric oxide
- :
-
peak, peak oxygen consumption
- DLCO:
-
lung diffusion of CO
- IPAQm:
-
International Physical Activity Questionnaire
- DLNO:
-
lung diffusion of NO
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Acknowledgments
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.
Funding
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.
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All the authors made substantial contributions to conception and design (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).
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Al Dandachi, G., Londner, C., Caumont-Prim, A. et al. Ageing and endurance training effects on quantity and quality of pulmonary vascular bed in healthy men. Respir Res 15, 8 (2014). https://doi.org/10.1186/1465-9921-15-8
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DOI: https://doi.org/10.1186/1465-9921-15-8
Keywords
- Physical activity
- Exercise
- Capillary blood volume
- Lung diffusion