Prerpints.org logo
Preprint
Article

Does Athletes' Respiratory Muscle Strength Affect Max VO2 Kinetics?

Altmetrics

Downloads

222

Views

107

Comments

0

Submitted:

15 March 2024

Posted:

18 March 2024

You are already at the latest version

Alerts
Abstract
The objective of this study was to investigate the impact of athletes' respiratory muscle strength, as assessed through maximal inspiratory (MIP) and expiratory pressure (MEP), on aerobic endurance, as indicated by maximal oxygen consump-tion (Max VO2) kinetics. Respiratory muscle strength was assessed using a digital spirometer (Pony FX Cosmed, Italy), while maximal oxygen utilization capacity was measured using a breath-by-breath automatic portable gas analysis system (Cosmed K5, Italy). Statistical analysis was conducted utilizing SPSS 22.0. Based on the standardized regression coefficients (β), it was found that MEP (mean ± SD: 130.95 ± 42.82) and inspiratory diaphragmatic circumference values significantly influenced ventilatory equivalent (VE), oxygen consumption (VO2), and carbon dioxide pro-duction (VCO2). Conversely, the remaining predictor variables did not exhibit a sig-nificant effect on VE (mean ± SD: 134.80 ± 36.69), VO2 (mean ± SD: 3877.52 ± 868.47 ml), and VCO2 (mean ± SD: 4301.27 ± 1001.07 ml). In contrast, measurements of chest circumference (mean ± SD: 91.40 ± 10.72 cm), MEP, and diaphragmatic cir-cumference during inspiration (mean ± SD: 95.20 ± 10.21 cm) were found to signifi-cantly impact Max VO2 (mean ± SD: 58.52 ± 10.74 ml/kg/min), while the other pre-dictor variables did not demonstrate a significant effect on Max VO2. Conclusively, the study revealed that measured values of diaphragmatic circumference during inspiration and MEP exerted a notable influence on Max VO2, VE, VO2, and VCO2. Our findings underscore the importance of considering respiratory muscle strength in assessing and enhancing athletes' aerobic performance. These insights contribute to a deeper understanding of the interplay between respiratory function and exercise capacity, offering potential avenues for optimizing training regimens and perfor-mance outcomes in athletic contexts.
Keywords: 
Subject: Public Health and Healthcare  -   Public Health and Health Services

1. Introduction

The respiratory capacity required to ensure adequate oxygen supply to the working muscles and removal of carbon dioxide is determined by the efficiency of gas exchange during external and internal respiration (1,2). Evaluation of functional response by gas analysis obtained during cardiopulmonary exercise test (CPET) is used as a gold standard to identify functional and pathophysiological limitations (1) for scuba divers, pilots, soldiers and professional athletes working under high levels of physical stress. During physical activity, lung ventilation increases with the oxygen requirement of the skeletal muscles and activates the accessory respiratory muscles next to the diaphragm (3). Respiratory muscle function is determined by the strength and endurance of the respiratory muscles (4). Many studies have shown that inspiratory muscles are fatigued after short periods of high-intensity exercise (5,6). and after long periods of moderate-intensity exercise (7). This fatigue may be a limiting factor that reduces exercise endurance (8,9). It has been determined that fatigue occurs in the diaphragm muscle with increased respiratory need during high intensity exercises of 85% of VO2max and above. Also, during these exercises, the respiratory muscles share the amount of oxygen consumed (10).
The results of previous studies show that active skeletal muscles and respiratory muscles share the cardiac output and the oxygen consumed during exercise. In order to increase the performance of the working skeletal muscles, it is important to provide respiration economically so that blood can be sent to the relevant parts at a higher rate. However, if the endurance of the respiratory muscles is not sufficient, it is predicted that exercise performance may decrease due to early fatigue of the diaphragm (11). High-intensity exercise causes peripheral vasoconstriction (12). In addition, it triggers the respiratory muscle metaboreflex, a high sympathetic nerve activity that limits blood flow to the working muscles and thus the energy output and consumption required for breathing (12,13).
The strenuous work of the inspiratory muscles is associated with significant neural and cardiovascular consequences. In healthy people, stimulation of inspiratory muscle fatigue by voluntary resistive inspiration has been seen to cause time-dependent increases in muscle sympathetic nerve activity, heart rate (HR) and mean arterial pressure (MAP), and a gradual decrease in arterial blood flow in inactive extremities (14). There is also evidence that the inspiratory muscle metaboreflex is activated by whole-body exercise. It has been seen that leg blood flow is inversely related to respiratory work during high-intensity exercise, and as a result, changes in leg vascular resistance are directly related to the extent of noradrenaline (norepinephrine) release (15). During prolonged intense whole-body exercise in healthy people, the metaboreflex response associated with inspiratory muscle fatigue may limit exercise performance (16). However, if the inspiratory muscle is exercised, triggering of the respiratory muscle metaboreflex can be delayed and performance can be increased (12). Based on the assumption that the role of respiratory muscle strength in athlete performance may be important for maximum effort; the aim of this study was to examine the effect of athletes’ respiratory muscle strength measured by maximal inspiratory and expiratory pressure on aerobic endurance (Max VO2) kinetics.

2. Materials and Methods

2.1. Study Design and Participant Selection

The participants included in the research consisted of 14 biathlon, 14 judo and 13 cross country athletes (22 men and 19 women), who applied to the Ministry of Youth and Sports, Department of Athlete Health, Performance and Service Quality Standards to become a volunteer participant. Inclusion criteria were being a non-smoker and not having a respiratory tract disease such as asthma, pulmonary tuberculosis, emphysema or chronic bronchitis. Athletes on medication, especially those on cardiac glycoside or β-receptor antagonist-derived drugs, were not included in the study. Athletes who met the inclusion criteria were evaluated on the same day.
After obtaining the demographic information of the athletes (age, year of sport, smoking habits, medication), RFT (respiratory function tests) tests were performed to evaluate respiration and respiratory muscle strength. The circumference measurements of the athletes were recorded by measuring the axilla and subcostal circumferences. Then, the athletes’ Max VO2 values were measured on the treadmill with a Cpet K5 device, and the data were recorded. The study was approved by Gazi University Ethics Committee (No: 2022-941). The study was conducted in accordance with the Declaration of Helsinki. All participants signed an informed consent form.
Table 1. Demographic information of the research group.
Table 1. Demographic information of the research group.
Characteristics Judo Biathlon Cross Country
Female (N=7) Male
(N=7)		 Female (N=6) Male
(N=8)		 Female (N=6) Male (N=7)
Sports Year (Year) 13.14±3.24 12.71±4.07 6.83±2.04 7.13±1.64 6.17±1.72 8.71±2.81
Age (Years) 22.63±3.06 22.62±4.80 19.24±1.46 18.73±2.21 17.83±1.34 20.21±2.81
Height (Cm) 163±7.57 175.93±6.99 161.33±5.06 170.63±4.72 161.42±6.00 174.57±8.40
Body Weight (Kg) 68.59±26.07 91.64±19.11 56.97±5.46 64.81±8.41 51.33±5.82 68.30±9.32

2.2. Data Collection Tools

2.2.1. Measurement of Chest Circumference

To assess the chest circumference accurately, two distinct methods were employed:
Axillary Circumference Measurement: This technique entailed the assessment of chest circumference at two pivotal junctures - during maximal expiration and maximal inspiration. The circumference was gauged from the level of the chest apex, encircling the axilla (or armpit), employing a rigid tape measure to ensure precision (17).
Subcostal Circumference Measurement: This approach aimed to capture variations in diaphragmatic circumference. Measurements were conducted during specific respiratory phases - mid-inspiration, maximal expiration, and maximal inspiration. The circumference was evaluated just below the ribcage, utilizing the same rigid tape measure for consistency across assessments (18)

2.2.2. Assessment of Respiratory Muscle Strength

Athletes were briefed on the procedures prior to the tests. Respiratory function and respiratory muscle strength were assessed utilizing a digital spirometer (Pony FX Cosmed, Italy). The evaluations were conducted with athletes seated comfortably in an upright position. Throughout the tests, participants utilized a mouthpiece and wore a nose clip. They were instructed to seal their lips tightly around the mouthpiece to prevent any air leakage from the spirometer. To familiarize athletes with the device’s operation, a few trial tests were conducted before the formal assessments. Each test was repeated thrice with a maximum rest period of three minutes between trials. The highest measurement score obtained was utilized for statistical analysis. During the maximal voluntary ventilation (MVV) test, athletes were directed to breathe deeply, rapidly, and forcefully for a duration of 12 seconds. Following the completion of the test, athletes were asked to briefly hold their breath to prevent respiratory alkalosis, and the MVV value was recorded. To evaluate respiratory muscle strength, maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP) tests were administered. For the MIP test, athletes were instructed to fully exhale before taking a deep, rapid, and forceful inhalation. Conversely, for the MEP test, athletes were prompted to inhale fully before exhaling swiftly and forcefully. Each test was repeated thrice with rest intervals between measurement cycles. The most favorable results obtained from all tests were selected for inclusion in the subsequent analysis.

2.2.3. Assessment of Aerobic Capacity (MaxVO2)

A breath-by-breath automatic portable gas analysis system (Cosmed K5, Italy) was used to measure the maximal oxygen utilization capacity and heart rate of the athletes. For this purpose, the athletes were asked to run at a constant speed of 5.0 km/h on the treadmill for 2 minutes, and then to run at an increasing speed of 0.016 km/h every second in accordance with the protocol. The athletes’ running was monitored in accordance with the test completion criteria used in treadmill protocols for aerobic capacity and power measurements.
The simultaneous observance of three of the following criteria was accepted as an indication that the maximal oxygen utilization capacity had been reached and the test was terminated. Athlete’s perception of fatigue on the original Borg scale rated as 17 or above and the athlete declaring to be exhausted, oxygen consumption no longer rising despite an increase in workload, ratio of carbon dioxide production to oxygen consumption (RQ) value reaching 1.15 and above, having a heart rate of 85% or more of the maximal heart rate, no increase in heart rate despite increased workload.The values measured in the last 30 seconds of aerobic capacity obtained with the automatic portable gas analysis program were averaged out and the ratios to the athletes’ body weight were calculated (19).In gas analysis, minute ventilation (VE), oxygen volume per minute (VO2), and carbon dioxide produced per minute (VCO2) were directly measured and recorded.

2.3. Statistical Analysis

Statistical analysis of the data was performed using IBM SPSS Version 21 (IBM Corp. Released 2012, Armonk, NY). The normal distribution of the data was assessed visually and with the Shapiro-Wilk test. The association between Max VO2, VE, VO2, and VCO2 values derived from the research cohort and respiratory parameters was examined using linear regression analysis. Statistical significance was determined at p < 0.05.

3. Results

The details of the statistical analyzes of the Max VO2, VE, VO2 and VCO2 parameters obtained from the research group are given in tabular format below.
According to Table 2, the parameters obtained from the research group show a high and significant relationship with MaxVO2/kg (R=.715, R2=.511, p<0.05). The mentioned variables together explain 51% of the total variance in Max VO2/kg. According to the standardized regression coefficient (β), Mid-Axilla circumference, MEP and Inspiratory Subcostal circumference values have a significant effect on MaxVO2, while the other predictor variables do not seem to have a significant effect on MaxVO2. When the bilateral and partial correlations between the predictor variables and MaxVO2 were examined, a negative correlation was observed between MIP, mid-axilla and axilla circumference measurements on inspiration and expiration and mid-subcostal and subcostal circumference measurements on inspiration and expiration. A positive relationship was determined between MEP and MVV values.
According to Table 3, the parameters obtained from the research group show a high and significant relationship with VE (R=.760, R2=.577, p<0.05). The mentioned variables together explain 57% of the total variance in VE. According to the standardized regression coefficient (β), the values of MEP and Inspiratory Subcostal circumference measurement have a significant effect on VE, while the other predictor variables do not seem to have a significant effect on VE. When the bilateral and partial correlations between the predictor variables and VE were examined, low level correlations were found between MIP and VE, and moderate and positive correlations with other parameters.
Table 4 shows that the parameters obtained from the research group show a high and significant relationship with VO2 (R=.814, R2=.663, p<0.05). The mentioned variables together explain 66% of the total variance in VO2. According to the standardized regression coefficient (β), the values of MEP and Subcostal circumference on inspiration have a significant effect on VO2, while the other predictor variables do not seem to have a significant effect on VO2. When the bilateral and partial correlations between predictor variables and VO2 were examined, low-level correlations were found between MIP and VO2, and moderate and positive correlations with other parameters.
In Table 5, it is seen that the parameters obtained from the research group show a high and significant relationship with VCO2 (R=.802, R2=.643, p<0.05). The mentioned variables together explain 64% of the total variance in VCO2. According to the standardized regression coefficient (β), the values of MEP and Inspiratory Subcostal circumference measurement have a significant effect on VCO2, while other the predictor variables do not seem to have a significant effect on VCO2. When the bilateral and partial correlations between the predictor variables and VCO2 were examined, low level correlations were found between MIP and VCO2, and moderate and positive correlations with other parameters.

4. Discussion

The objective of this study was to investigate the influence of athletes’ respiratory muscle strength, evaluated through maximal inspiratory (MEP) and expiratory pressure (MEP), on aerobic endurance, as delineated by maximal oxygen consumption (Max VO2) kinetics. 16% of oxygen intake during exercise is used by the respiratory muscles. Taking this into consideration, the effect of the respiratory muscles on performance is non-negligible (20). Inspiration is an active process both at rest and in exercise. The diaphragm is the primary inspiratory muscle, and its mitochondrial volume density, oxidative capacity and aerobic capacity of muscle fibers are four times higher than most other skeletal muscles. The other important inspiratory muscles are the intercostal muscles. The diaphragm or intercostals alone provide adequate breathing in the resting state, while the efficiency of the diaphragm decreases during vigorous exercise; the scalene muscles, pectoralis minor and sternocleidomastoid muscles are gradually activated to assist inspiration (20). During resting breathing, expiration is passive as the rib cage and lungs tend to return to their original state due to their flexible structure. Intercostal muscles that are activated during exercise are responsible for forced expiration. When ventilation is increased, lung contraction also increases as a result of active contractions of the expiratory muscles that decrease the intrathoracic volume (21).
Upon analyzing the findings of our study, we noted a negative correlation between Max VO2 and measurements of circumference at the mid-axilla and axilla during both inspiration and expiration, as well as at the mid-subcostal and subcostal regions during inspiration and expiration. Conversely, positive correlations were observed between maximal expiratory pressure (MEP) and maximal voluntary ventilation (MVV). These findings imply an enhanced ventilatory response during exercise, wherein greater expiratory muscle strength and maximal voluntary ventilation capacity lead to increased respiratory frequency. Consequently, this facilitates the rapid removal of carbon dioxide and enhanced uptake of oxygen during physical exertion.
In the literature, Klusiewicz (2014) could not find a correlation between the MIP value and absolute or relative max VO2 values in male athletes, but he found a correlation between the MIP value and absolute or relative max VO2 values in female athletes. In our study, no significant relationship could be found between relative maxVO2 and MIP measurement results, which suggests that the athletes in our study reached their Max VO2 value before reaching their maximum inspiratory muscle strength potential (22).
Previous studies in the literature mostly explain the effect of respiratory muscle strengthening training on MaxVO2. For example, Lomax et al. (2011) reported that respiratory muscle training and warm-up of the respiratory muscles (at 40% of the maximal inspiratory muscle strength) on 12 male football players consisting of two groups increased their Yo-Yo test performance compared to the control group (23). Volianitis et al. (2001) reported in a study they conducted on female rowing athletes that the athletes’ maxVO2 value after respiratory muscle warm-up exercise performed with branch-specific general warm-up was higher than that of the experimental group (24). In contrast, Amonette and Dupler (2002) reported in a study that breathing exercises did not cause an improvement in maxVO2 capacity (25). In another study conducted on young football players, it was reported that there was no significant change in maxVO2 values after a four-week respiratory muscle training program (26). Romer et al. (2002) found that there was no significant change in the maxVO2 values of the subjects after respiratory muscle training (9).
During high-intensity endurance exercise, excessive metabolic CO2 production can only be removed by increased ventilation. If respiratory muscle strength or endurance remains below the increased demand for ventilation, tissue and blood CO2 will increase, causing metabolic acidosis and thus failure of both skeletal and respiratory musculature, which signifies the importance of expiratory muscle strength. We determined that the moderate positive correlation findings between MEP and VCO2 in our study prove the importance of expiratory muscle strength. In our study, it was determined that the values of subcostal circumference measurement in MEP and on inspiration had a significant effect on VE. In line with this result, it can be predicted that since the amount of air entering the lungs per minute will increase with the development of respiratory muscles, sports performance will also increase positively.
Efficient utilization of respiratory muscles holds paramount importance during prolonged aerobic activities. It is postulated that enhanced economy in the functioning of respiratory musculature correlates with improved exercise performance (27). Thus, it becomes imperative to augment respiratory muscle strength through training to bolster overall exercise capacity. Endurance training is believed to defer fatigue onset in respiratory muscles while concurrently enhancing oxygen utilization efficiency. With the advancement of respiratory muscle development, it is anticipated that the volume of air intake will rise, consequently leading to a positive augmentation in sports performance (3).
The practical applications of our study’s findings hold significance for athletes, coaches, and sports scientists alike. Incorporating specific respiratory muscle training into athletes’ conditioning regimens can improve their respiratory muscle strength, thereby enhancing their overall aerobic capacity and endurance. This may involve exercises such as inspiratory muscle training (IMT) or expiratory muscle training (EMT) targeting the muscles involved in respiration. Moreover, understanding the relationship between respiratory muscle strength and aerobic performance allows for more effective performance optimization strategies. Coaches and trainers can use this knowledge to develop individualized training plans that address athletes’ specific respiratory needs, ultimately maximizing their athletic potential. Additionally, strengthening respiratory muscles not only improves performance but also contributes to injury prevention. Enhanced respiratory muscle strength can help athletes maintain proper breathing mechanics during strenuous exercise, reducing the risk of fatigue-related injuries and respiratory distress. Lastly, regular assessment of respiratory muscle strength can serve as a valuable tool for monitoring athletes’ progress and identifying areas for improvement. Integrating objective measures, such as maximal inspiratory and expiratory pressure assessments, into routine performance evaluations enables coaches and sports scientists to track changes in respiratory function over time and adjust training protocols accordingly.
Despite the valuable insights gained from this study, several limitations should be acknowledged. First, the sample size in this study may limit the generalizability of the findings to broader athlete populations. Future research with larger and more diverse samples is needed to validate the observed associations across different sports and athletic levels. Second, the cross-sectional nature of this study precludes establishing causality between respiratory muscle strength and aerobic endurance. Longitudinal studies are warranted to elucidate the temporal relationships between these variables and better understand the effects of respiratory muscle training over time. Third, the laboratory-based setting of this study may not fully replicate the real-world conditions in which athletes train and compete. The transferability of the findings to actual sporting environments warrants consideration, as performance outcomes may be influenced by additional factors not captured in controlled laboratory settings. Acknowledging these limitations provides valuable insights into the scope and interpretation of the study findings. Addressing these limitations in future research endeavors will contribute to a more comprehensive understanding of the complex interplay between respiratory muscle strength and athletic performance.

5. Conclusions

Our investigation elucidates the substantial influence of respiratory muscle strength, notably measured through maximal inspiratory and MEP, on various physiological parameters related to aerobic endurance among athletes. Specifically, our results reveal significant associations between MEP and inspiratory diaphragmatic circumference values with VE, VO2, and VCO2. Moreover, the measured values of diaphragmatic circumference during inspiration and MEP significantly impact Max VO2. These findings underscore the pivotal role of respiratory muscle strength in shaping athletes’ aerobic performance profiles. Such insights provide valuable implications for tailored training strategies aimed at optimizing athletes’ respiratory function and overall endurance capacity. Lastly, the practical applications of our study underscore the importance of integrating respiratory muscle training into athletes’ preparation and conditioning programs. By optimizing respiratory function, practitioners can enhance athletes’ aerobic performance, reduce the risk of injury, and ultimately support their pursuit of athletic excellence.

Author Contributions

Conceptualization, G.D, B.K., V.O.Ç., H. İ. C., M.R., S.V.; methodology, G.D, H. İ. C., M.R., S.V; formal analysis, H. İ. C., M.R., S.V; investigation, G.D, B.K., V.O.Ç.; writing—original draft preparation, G.D, B.K., V.O.Ç., H. İ. C., M.R., S.V; writing—review and editing, G.D, B.K., V.O.Ç., H. İ. C., M.R., S.V; supervision, H. İ. C., S.V; funding acquisition, M.R., S.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Ethics approval, consents to participate and all procedures were in accordance with the ethical standards prescribed by the institutional and/or national research committee for studies involving human participants and with the 1964 Helsinki Declaration. This cross-sectional study was approved (No: 2022-941) by Gazi University Ethics Committee and conducted in line with the Declaration of Helsinki.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author.

Acknowledgments

We thank to participants

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Balady, G.J.; Arena, R.; Sietsema, K.; Myers, J.; Coke, L.; Fletcher, G.F.; Forman, D.; Franklin, B.; Guazzi, M.; Gulati, M.; et al. Clinician’s Guide to Cardiopulmonary Exercise Testing in Adults. Circulation 2010, 122, 191–225. [Google Scholar] [CrossRef] [PubMed]
  2. Martin, B.; Chen, H.-I. Ventilatory Endurance in Athletes: a Family Study. Int. J. Sports Med. 1982, 03, 100–104. [Google Scholar] [CrossRef] [PubMed]
  3. Wilcox, P.; Road, J.; Altalag, A. Exercise Testing. Pulmonary Function Tests in Clinical Practice 2009, 157–216. [Google Scholar]
  4. ATS/ERS Statement on Respiratory Muscle Testing. Am. J. Respir. Crit. Care Med. 2002, 166, 518–624. [CrossRef] [PubMed]
  5. Martin, B.J.; Stager, J.M. Ventilatory endurance in athletes and non-athletes. Med. Sci. Sports Exerc. 1981, 13, 21–26. [Google Scholar] [CrossRef] [PubMed]
  6. Volianitis, S.; Mcconnell, A.K.; Koutedakis, Y.; Mcnaughton, L.; Backx, K.; Jones, D.A. Inspiratory muscle training improves rowing performance. Med. Sci. Sports Exerc. 2001, 33, 803–809. [Google Scholar] [CrossRef] [PubMed]
  7. Hill, N.S.; Jacoby, C.; Farber, H.W. Effect of an endurance triathlon on pulmonary function. Med. Sci. Sports Exerc. 1991, 23, 1260–1264. [Google Scholar] [CrossRef] [PubMed]
  8. Mador, M.J.; Acevedo, F.A.; Hirai, D.M.; Jones, J.H.; Zelt, J.T.; da Silva, M.L.; Bentley, R.F.; Edgett, B.A.; Gurd, B.J.; Tschakovsky, M.E.; et al. Effect of respiratory muscle fatigue on subsequent exercise performance. J. Appl. Physiol. 1991, 70, 2059–2065. [Google Scholar] [CrossRef]
  9. Romer, L.M.; McConnell, A.K.; Jones, D.A. Effects of inspiratory muscle training on time-trial performance in trained cyclists. J. Sports Sci. 2002, 20, 547–590. [Google Scholar] [CrossRef]
  10. Dempsey, J.A.; Amann, M.; Romer, L.M.; Miller, J.D. Respiratory System Determinants of Peripheral Fatigue and Endurance Performance. Med. Sci. Sports Exerc. 2008, 40, 457–461. [Google Scholar] [CrossRef]
  11. A Babcock, M.; Pegelow, D.F.; A Harms, C.; A Dempsey, J. Effects of Respiratory Muscle Unloading on Exercise-induced Diaphragm Fatigue. Cardiopulm. Phys. Ther. J. 2002, 13, 32. [Google Scholar] [CrossRef]
  12. Harms, C.A. Effect of skeletal muscle demand on cardiovascular function. Med. Sci. Sports Exerc. 2000, 32, 94–99. [Google Scholar] [CrossRef] [PubMed]
  13. Romer, L.M.; Lovering, A.T.; Haverkamp, H.C.; Pegelow, D.F.; Dempsey, J.A. Effect of inspiratory muscle work on peripheral fatigue of locomotor muscles in healthy humans. J. Physiol. 2006, 571, 425–439. [Google Scholar] [CrossRef]
  14. Sheel, A.W.; Derchak, P.A.; Morgan, B.J.; Pegelow, D.F.; Jacques, A.J.; Dempsey, J.A. Fatiguing inspiratory muscle work causes reflex reduction in resting leg blood flow in humans. J. Physiol. 2001, 537, 277–289. [Google Scholar] [CrossRef] [PubMed]
  15. Harms, C.A.; Babcock, M.A.; McClaran, S.R.; Pegelow, D.F.; Nickele, G.A.; Nelson, W.B.; Dempsey, J.A.; Welch, J.F.; Archiza, B.; Guenette, J.A.; et al. Respiratory muscle work compromises leg blood flow during maximal exercise. J. Appl. Physiol. 1997, 82, 1573–1583. [Google Scholar] [CrossRef] [PubMed]
  16. Johnson, B.D.; A Babcock, M.; E Suman, O.; A Dempsey, J. Exercise-induced diaphragmatic fatigue in healthy humans. J. Physiol. 1993, 460, 385–405. [Google Scholar] [CrossRef] [PubMed]
  17. Mondal, P. B.; Mridha, S. A study on selected anthropometric characteristics of heightweight matched female athletes and non-athletes. J Sports Phys Educ 2015, 2, 41–45. [Google Scholar] [CrossRef]
  18. Daşkapan, A.; Şanlı, C.; Aydoğan-Arslan, S.; Çiledağ-Özdemir, F.; Korkem, D.; Kara, U. Evaluation of the functional capacity, respiratory functions and musculoskeletal systems of the children with chest pain for non-cardiac reasons. Turk. J. Pediatr. 2017, 59, 295–303. [Google Scholar] [CrossRef]
  19. Powers, S. K.; Howley, E. T. Exercise Physiology: Theory and Application to Fitness and Performance; McGraw-Hill Humanities/Social Sciences/Languages, 2003. [Google Scholar]
  20. Janssens, L.; Brumagne, S.; McConnell, A.K.; Raymaekers, J.; Goossens, N.; Gayan-Ramirez, G.; Hermans, G.; Troosters, T. The assessment of inspiratory muscle fatigue in healthy individuals: A systematic review. Respir. Med. 2013, 107, 331–346. [Google Scholar] [CrossRef]
  21. Jurić, I.; Labor, S.; Plavec, D.; Labor, M. Inspiratory muscle strength affects anaerobic endurance in professional athletes. Arch. Ind. Hyg. Toxicol. 2019, 70, 42–48. [Google Scholar] [CrossRef]
  22. Klusiewicz, A.; Długołęcka, B.; Charmas, M. Characteristics of the respiratory muscle strength of women and men at different training levels. Pol. J. Sport Tour. 2014, 21, 82–86. [Google Scholar] [CrossRef]
  23. Lomax, M.; Grant, I.; Corbett, J. Inspiratory muscle warm-up and inspiratory muscle training: Separate and combined effects on intermittent running to exhaustion. J. Sports Sci. 2011, 29, 563–569. [Google Scholar] [CrossRef] [PubMed]
  24. Volianitis, S.; Mcconnell, A.K.; Koutedakis, Y.; Jones, D.A. Specific respiratory warm-up improves rowing performance and exertional dyspnea. Med. Sci. Sports Exerc. 2001, 33, 1189–1193. [Google Scholar] [CrossRef] [PubMed]
  25. Amonette, W.; Dupler, T. The effects of respiratory muscle training on VO2max, the ventilatory threshold and pulmonary function. Journal of Exercise Physiology 2002, 5, 29–35. [Google Scholar]
  26. Ozgider, C. In young soccer players, four weeks of respiratory muscle training improves recovery performance, but does not improve respiratory function and maximum oxygen utilization capacity (VO2max); Middle East Technical University, Institute of Social Sciences: Ankara, 2009. [Google Scholar]
  27. Demir, M.; Filiz, K. The effects of sports exercises on the human organism. Kirsehir Education Faculty Journal 2004, 5. [Google Scholar]
Table 2. Regression analysis results regarding MaxVO2/kg (X=58.52±10.74 ml/kg/min) prediction of the parameters obtained from the study group.
Table 2. Regression analysis results regarding MaxVO2/kg (X=58.52±10.74 ml/kg/min) prediction of the parameters obtained from the study group.
Characteristics X Sd B SH β T p Zero-order Partial
(Constant) 131.529 17.495 7.518 0
MIP (Cm/H2O) 99.08 29.7 -0.098 0.065 -0.271 -1.504 0.143 -0.092 -0.265
MEP (Cm/H2O) 130.95 42.82 0.148 0.048 0.59 3.091 0.004 0.108 0.491
Mid-Axilla Circumference (Cm) 91.4 10.72 -3.498 1.642 -3.489 -2.13 0.041 -0.42 -0.363
Axilla Circumference On Inspiration (Cm) 95.2 10.216 0.511 0.932 0.486 0.548 0.588 -0.405 0.1
Axilla Circumference On Expiration (Cm) 89.13 10.827 1.926 1.313 1.941 1.467 0.153 -0.405 0.259
Mid-Subcostal Circumference (Cm) 78.82 10.454 1.064 1.072 1.035 0.993 0.329 -0.344 0.178
Subcostal Circumference On Inspiration (Cm) 82.95 9.462 -1.329 0.681 -1.17 -1.953 0.045 -0.366 -0.336
Subcostal Circumference On Expiration (Cm) 76.63 10.505 0.42 0.939 0.41 0.447 0.658 -0.34 0.081
MVV 135.63 38.39 0.08 0.05 0.286 1.603 0.12 0.027 0.281
F(9-30)=3.477 P=.005
R=.715 R2=.511
MIP: Maximum inspiratory pressure, MEP: Maximum expiratory pressure, MVV: Maximum voluntary ventilation.
Table 3. Regression analysis results regarding VE (X=134.80±26.69 ml) prediction of the parameters obtained from the study group.
Table 3. Regression analysis results regarding VE (X=134.80±26.69 ml) prediction of the parameters obtained from the study group.
Characteristics X SD B SH Β T p Zero-Order Partial
(Constant) 123.729 40.390 3.063 .005
MIP (Cm/H2o) 99.08 29.70 -.111 .151 -.124 -.737 .467 .364 -.133
MEP (Cm/H2o) 130.95 42.82 .338 .111 .543 3.061 .005 .565 .488
Mid-Axilla Circumference (Cm) 91.40 10.720 -4.127 3.790 -1.658 -1.089 .285 .510 -.195
Axilla Circumference On Inspiration (Cm) 95.20 10.216 -.233 2.152 -.089 -.108 .915 .492 -.020
Axilla Circumference On Expiration (Cm) 89.13 10.827 3.552 3.031 1.441 1.172 .251 .515 .209
Mid-Subcostal Circumference (Cm) 78.82 10.454 2.796 2.475 1.095 1.130 .267 .509 .202
Subcostal Circumference On Inspiration (Cm) 82.95 9.462 -3.838 1.571 -1.361 -2.443 .021 .419 -.407
Subcostal Circumference On Expiration (Cm) 76.63 10.505 1.849 2.168 .728 .853 .400 .524 .154
MVV 135.63 38.39 .124 .115 .178 1.073 .292 .534 .192
F(9-30)=4.552 P=.001
R=.760 R2=.577
MIP: Maximum inspiratory pressure, MEP: Maximum expiratory pressure, MVV: Maximum voluntary ventilation. VE: Minute Ventilation.
Table 4. Regression analysis results regarding VO2 (Xort=3877.52±868.47 ml) prediction of the parameters obtained from the study group.
Table 4. Regression analysis results regarding VO2 (Xort=3877.52±868.47 ml) prediction of the parameters obtained from the study group.
Characteristics X SD B SH Β T p Zero-Order Partial
(Constant) 1716.990 1173.112 1.464 .154
MIP (Cm/H2o) 99.08 29.70 -7.307 4.376 -.250 -1.670 .105 .347 -.292
MEP (Cm/H2o) 130.95 42.82 11.606 3.210 .572 3.616 .001 .624 .551
Mid-Axilla Circumference (Cm) 91.40 10.720 -187.015 110.081 -2.308 -1.699 .100 .597 -.296
Axilla Circumference On Inspiration (Cm) 95.20 10.216 44.433 62.518 .523 .711 .483 .607 .129
Axilla Circumference On Expiration (Cm) 89.13 10.827 129.642 88.048 1.616 1.472 .151 .602 .260
Mid-Subcostal Circumference (Cm) 78.82 10.454 76.020 71.878 .915 1.058 .299 .621 .190
Subcostal Circumference On Inspiration (Cm) 82.95 9.462 -81.135 45.639 -.884 -1.778 .086 .562 -.309
Subcostal Circumference On Expiration (Cm) 76.63 10.505 34.126 62.958 .413 .542 .592 .625 .098
MVV 135.63 38.39 5.857 3.350 .259 1.748 .091 .584 .304
F(9-30)=6.562 P=.000
R=.814 R2=.663
MIP: Maximum Inspiratory Pressure, MEP: Maximum Expiratory Pressure, MVV: Maximum Voluntary Ventilation.
Table 5. Regression analysis results regarding VCO2 (Xort=4301.27±.1001.07 ml) prediction of the parameters obtained from the study group.
Table 5. Regression analysis results regarding VCO2 (Xort=4301.27±.1001.07 ml) prediction of the parameters obtained from the study group.
Characteristics X SD B SH Β T p Zero-Order Partial
(Constant) 2314.699 1392.589 1.662 .107
MIP (Cm/H2o) 99.08 29.70 -10.586 5.195 -.314 -2.038 .050 .279 -.349
MEP (Cm/H2o) 130.95 42.82 14.358 3.810 .614 3.769 .001 .590 .567
Mid-Axilla Circumference (Cm) 91.40 10.720 -193.217 130.677 -2.069 -1.479 .150 .588 -.261
Axilla Circumference On Inspiration (Cm) 95.20 10.216 17.688 74.215 .181 .238 .813 .590 .043
Axilla Circumference On Expiration (Cm) 89.13 10.827 154.760 104.521 1.674 1.481 .149 .593 .261
Mid-Subcostal Circumference (Cm) 78.82 10.454 116.701 85.326 1.219 1.368 .182 .614 .242
Subcostal Circumference On Inspiration (Cm) 82.95 9.462 -104.461 54.177 -.987 -1.928 .043 .547 -.332
Subcostal Circumference On Expiration (Cm) 76.63 10.505 28.444 74.737 .299 .381 .706 .618 .069
MVV 135.63 38.39 4.590 3.977 .176 1.154 .257 .527 .206
F(9-30)=5.996 P=.000
R=.802 R2=.643
MIP: Maximum Inspiratory Pressure, MEP: Maximum Expiratory Pressure, MVV: Maximum Voluntary Ventilation.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
Prerpints.org logo

Preprints.org is a free preprint server supported by MDPI in Basel, Switzerland.

facebook logotwitter logolinkedin logo
MDPI Initiatives
Important Links
Subscribe

Disclaimer

Terms of Use

Privacy Policy

© 2024 MDPI (Basel, Switzerland) unless otherwise stated