Exaggerated Response of Systolic Blood Pressure to Cycle Ergometer

Article information

Ann Rehabil Med. 2013;37(3):364-372
Publication date (electronic) : 2013 June 30
doi : https://doi.org/10.5535/arm.2013.37.3.364
1Department of Rehabilitation Medicine, Inje University Sanggye Paik Hospital, Seoul, Korea.
2Division of Physical Education, Soonchunhyang University, Cheonan, Korea.
3Sport Science Institute, Korea National Sport University, Seoul, Korea.
Corresponding author: Chul-Hyun Kim. Sport Science Institute, Korea National Sport University, 1239 Yangjae-daero, Songpa-gu, Seoul 138-763, Korea. Tel: +82-2-410-6692, Fax: +82-2-410-6945, kimch37@gmail.com
Received 2012 July 25; Accepted 2012 October 26.

Abstract

Objective

The aim of this study is to exam the effects of exercise modes on the systolic blood pressure and rate-pressure product during a gradually increasing exercise load from low to high intensity.

Methods

Fifteen apparently healthy men aged 19 to 23 performed the graded exercise tests on cycle ergometer (CE) and treadmill (TM). During the low-to-maximal exercises, oxygen uptake (VO2), heart rate (HR), systolic blood pressure (SBP) and rate-pressure product were measured.

Results

CE had a significantly lower maximum VO2 than TM (CE vs. TM: 48.51±1.30 vs. 55.4±1.19 mL/kg/min; p<0.001). However, CE showed a higher maximum SBP (SBPmax) at the all-out exercise load than TM (CE vs. TM: 170±2.4 vs. 154±1.7 mmHg; p<0.001). During the low-to-maximal intensity increment, the slope of the HR with VO2 was the same as VO2 increased in times of the graded exercise test of CE and TM (CE vs. TM: 2.542±0.100 vs. 2.506±0.087; p=0.26). The slope of increase on SBP accompanied by VO2 increase was significantly higher in CE than in TM (CE vs. TM: 1.669±0.117 vs. 1.179±0.063; p<0.001).

Conclusion

The SBP response is stronger in CE than in TM during the graded exercise test. Therefore, there is a possibility that CE could induce a greater burden on workloads to cardiovascular system in humans than TM.

INTRODUCTION

The graded exercise test is a test that analyzes the change in the body's respiratory gas, electrocardiogram, or blood pressure (BP), which is induced by gradually increasing the workload with the use of a cycle ergometer (CE) or a treadmill (TM) [1]. This test can detect latent cardiovascular diseases and evaluate cardiovascular function [2]. It is particularly useful for evaluating the cardiopulmonary capacity of athletes and normal people, as well as for clinical practice, such as diagnosis and evaluation of cardiovascular disease, assessment of treatment effect, ascertainment of pathophysiology, and exercise prescription for rehabilitation [3-6]. To perform the graded exercise test, a protocol and mode of exercise testing should first be decided upon. The protocol for the exercise stress test consists of standardized gradual increments of exercise workload (oxygen uptake [VO2]) from the resting phase to the maximal workload [1,2]. An appropriate exercise protocol can be decided upon according to the absence or presence of disease, age, and physical activity level of the examinee [7,8]. The two major modes for the graded exercise test are CE and TM. TM involves a higher exercise load than CE. Since most people are more accustomed to walking than to riding a bicycle, TM is generally preferred over CE [4,8,9].

Several protocols for the graded exercise test have been developed, and the observable physiological features of the two modes of exercise test (CE and TM) have been studied. The hemodynamic responses to TM and CE in the exercise tolerance test have established that VO2max (maximum oxygen uptake) was higher in TM than in CE. Therefore, the level and mechanism of the hemodynamic response differ in modes of the graded exercise test [7-11].

The results of previous studies, however, were only about hemodynamic responses to modes of exercise testing under the maximal exercise workload. Moreover, the hemodynamic changes that result from gradual increments in the exercise load, from low to maximal intensity, in TM and CE have not been successfully compared. Particularly, the systolic blood pressure (SBP) response to increased heart rate (HR) and VO2 in TM and CE has not yet been clearly identified [7-13]. Reed [12] reported that SBPs at 40% and 60% HR reserve was higher in CE than in TM. Also, it is reported that SBP at the maximum workload was higher in CE than in TM [9]. These results indicate that the degree of increase in SBP on the CE is likely to be higher than the degree of increase in SBP on the TM. As the increased SBP in CE could increase the myocardial burden of patients with BP-related diseases such as ischemic cardiovascular disease, hypertension, and aneurysm, which may have an adverse effect [14], it should carefully be considered in the exercise test and exercise prescription. Thus, the information on the differences in the increment level of SBP between CE and TM is necessary for making an exercise prescription.

Previous studies on the differences of SBP between different modes of exercise testing were based, however, on the HRs instead of VO2 as the criterion for the exercise workload, and used uniform intensities of the exercise workload instead of gradually increasing the exercise load from low to maximal intensity. Therefore, not much information on BP has been seen in the hemodynamic responses (particularly SBP) to graded exercise increments in the exercise load (VO2) from low to high intensity in CE and TM exercise.

This study hypothesized that the SBP and rate-pressure rate during cycle ergometer exercise could be higher than SBP and rate-pressure rate during a TM exercise at the given low-to-maximal exercise load expressed as VO2. The aim of this study is to exam the effects of exercise modes on the SBP and rate-pressure product (RPP) during a gradually increasing exercise load from low to high intensity.

MATERIALS AND METHODS

Subjects

Fifteen apparently healthy males who have no known diseases and live independently were recruited from a physical education college to take part in the study. All participants, who regularly performed graded exercise test at least two times a year for three years, were highly motivated and accustomed to the performance of exhaustive tests on both the bicycle ergometer and TM. The participation criteria were as follows: 1) nonsmoking; 2) age≥19 and ≤23; 3) involvement in structured physical activity (i.e., regular moderate-to-high activity more than 240 min/wk) in the 8 months previous to the study; 4) absence of medication; and 5) absence of any medical or orthopedic condition aggravated by exercise. These inclusion criteria were selected for earning stable cardiovascular response to the graded exercise test. Participants gave written, informed consent after the experimental procedures and the associated risks as well as the benefits of participation were fully explained. All subjects were recruited through advertisements in local media. Sixty persons were interviewed on this study and 29 subjects voluntarily participated in this experiment. Among 29 subjects, 14 participants were dropped out because of unstable response to the graded exercise tests. Fifteen participants finally completed all the experiments of this study. Therefore, the compliance in the present study was 51.7%. Written informed consent was obtained from all subjects. Institutional Review Board (IRB) approved the procedure and study design of this study (IRB serial no. 10-107).

Exercise tests

Participants were instructed to arrive at the laboratory in a rested state, at least 3-hour postprandial, to avoid strenuous exercise and alcohol in the 48 hours preceding a test session. They were weighted (kg) and had their height (cm) measured, and were fitted with a Heart Rate Monitor (Polar Electro, Kempele, Finland). Participants then completed a medical history and physical activity questionnaire. After allowing a ten-minute seated rest period, HR and BP were measured at rest by a Heart Rate Monitor and a mercury sphygmomanometer. Cardiopulmonary responses to exercise were measured during a graded CE model T300 (COSMED, Rome, Italy) and TM tests model Excalibur Sport (Lode B.V., Groningen, Netherlands) on two different days with an interval of one week in random sequence. Room temperature was 20℃-24℃ and relative humidity was 45%-55%. TM testing was performed according to the Bruce protocol [1], which consists of three-minute increments of TM speed and incline, starting at a speed of 2.74 km/h and a gradient of 10%, increasing in gradient by 2% every 3 minutes in line with simultaneous increments of speed of 2.74, 4.02, 5.47, 6.76, 8.05, and 8.85 km/h. The graded cycle ergometer testing used a Bruce ramp protocol that consists of continuous work rate increments [1]. With the pedaling cadence at 70 rpm, the work rate increased as a ramp of 35 W/min to achieve maximal power output within 8 to 12 minutes of the test. Both test modes included a warm-up period consisting of stretching exercises and a three-minute walk at 6.0 km/h or a three-minute pedaling at 70 rpm with a load at 20 W. The two protocols were comparable for gradually increasing loads and reaching the all-out load even though the Bruce ramp protocol produced continuously increased loads because the sum of the three-minute increased loads at each three-minute-long stage were comparable with each stage of Brue protocol for TM [1,2]. During CE and TM tests, VO2, HR, BP, and the Borg-rated perceived exertion were recorded per minute starting from the baseline, starting from two and at maximal exercise. VO2, carbon dioxide production, and gas exchange ratio were measured on a breath-by-breath basis by a gas analyzer K4b2 (COSMED). The HR was determined with a Heart Rate Monitor, and BP was measured with a mercury sphygmomanometer by a trained technician under supervision of a physician. The Borg-rated perception of exertion was attained through direct communication by using the Borg scale. The RPP were obtained by multiplying the HR by SBP (RPP=HR×SBP). The establishment of a maximal VO2 (VO2max) for each participant was evaluated against the criteria (a plateau in VO2, Borg-rated perceived exertion 19 or 20, HR within ±10 beats of age-related maximum and a respiratory exchange ratio >1.15) and confirmed if three of them were met. The gas analyzer was calibrated with mixed calibration gas every 5 exercise tests.

Statistical analysis

Based on the power analysis with G-power 3.0 program [14], it is estimated that at least 15 patients were requited to detect the mean differences in VO2, HR, SBP, and RPP between CE and TM, with a statistical power of 80%, type I error of 0.05, effects size of 0.7 and one-tailed test. To compensate for a possible exclusion, 29 subjects were first enrolled and after a dropout of 14 subjects (51.7% of compliance). 15 subjects finally completed this study. Descriptive statistics were used for all the variables, and all values were presented as the means and standard errors. Comparisons of individual data between exercise modes were performed using Wilcoxon matched-pairs singed-ranks test. For estimating the increment ratios of the HR-to-VO2, SBP-to-VO2, RPP-to-VO2, and SBP-to-HR, the binary linear regression analysis was conducted with the model of ender. Independent variable was VO2 with the dependent variables of HR, VO2, and RPP, respectively. Independent variable was also HR with SBP. With calculating the binary linear regression analysis, beta value was used for the slope of equation and constant value was used for y-intercept in the regression equation. F-value was identified for the significance of the equation model. The variance inflating factor (VIF) was calculated on the regressions of VO2-HR, VO2-SBP, VO2-RPP, and HR-VO2 and the values of VIF were 1.000 in all of the regression analyses. Pearson product moment coefficients (r) were used to assess the significance of relationships of hemodynamic response variables. The statistical significance level was set at p<0.05 with the one-tailed test. All analyses were performed using SPSS ver. 11.0 (SPSS Inc., Chicago, IL, USA).

RESULTS

Fifteen healthy male participants all obtained the resting-to-maximal VO2 by reaching all-out intensity in a gradual stress test on CE and TM. Their general characteristics were shown at (Table 1), including age, physique, HR, and BP at resting. As shown in (Fig. 1), the VO2max on CE was significantly lower than that on TM (CE vs. TM: 48.51±1.30 vs. 55.4±1.19 mL/kg/min; p<0.001). At this status, the maximum heart rate (HRmax) was significantly lower in CE than TM (CE vs. TM: 177±2.4 vs. 188±2.3 beats/min; p<0.001), while maximum systolic blood pressure (SBPmax) in CE was significantly higher than in TM (CE vs. TM: 170±2.4 vs. 154±1.7 mmHg, p<0.001), leading to a significantly higher load in the maximum rate-pressure product (RPPmax) in CE compared to RPPmax in TM (CE vs. TM: 30,149±678 vs. 28,971±295; p<0.05). In other words, CE had lower VO2max and HRmax than TM at the level of aerobic maximal capacity, and showed high SBPmax and RPPmax.

Table 1

Characteristics of subjects (n=15)

Fig. 1

Hemodynamic differences between cycle ergometer (CE) and treadmill (TM) at the maximum level of workload (n=15). VO2max, maximum oxygen uptake; HRmax, maximum heart rate; SBPmax, maximum systolic blood pressure; RPPmax, maximum rate-pressure product.

From the graded exercise tests on the CE and TM reaching from low intensity to maximal intensity, patterns of responses of HR, SBP, and RPP for gradually increasing load VO2 are as in (Fig. 2). HR, SBP, and RPP proportionally increased as VO2 increased, but SBP and RPP of CE were higher than TM, except that HRs of CE and TM maintained the same level with each other in terms of the width and slope for the increase.

Fig. 2

An example of hemodynamic patterns of the heart rate, systolic blood pressure (SBP) and rate-pressure product (RPP) according to the work rates on cycle ergometer (CE) and treadmill (TM) during the gradual exercise test (n=1). VO2, oxygen uptake.

The results of a slope of the line from relation of HR, SBP, and RPP with VO2 or SBP for fifteen participants (Fig. 3). While the increment of the HR-VO2 appeared to be the same as VO2 increased in times of graded exercise test of CE and TM (p=0.26), the slope of SBP increase and RPP accompanied by VO2 increase (SBP-VO2 and RPP-VO2, respectively) were all significantly higher in CE than in TM (p<0.001). On the other hand, on the standard of the HR, not VO2, for exercise load, SBP accompanied by the increase of exercise load (HR) elevated with a stiffer slope in CE than in TM (p<0.001). In the end, SBP in times of gradually increasing exercise load for CE increased relatively a lot in TM, and RPP too elevated to a high level as a result.

Fig. 3

The slope differences between cycle ergometer (CE) and treadmill (TM) exercise during the graded exercise test. (A) Slope for heart rate (HR) to oxygen uptake (VO2): HR is the y-axis and VO2 is the x-axis. (B) Slope for systolic blood pressure (SBP) to VO2: SBP is the y-axis and VO2 is the x-axis. (C) Slope of rate-pressure product (RPP) to VO2: RPP is the y-axis and VO2 is the x-axis. (D) Slope for HR to SBP: HR is the y-axis and SBP is the x-axis. All values are mean±standard error.

DISCUSSION

In this study, two modes of exercise tests (CE and TM exercise) were performed with gradual increments in the exercise workload from low to maximal intensity, to identify the differences in the hemodynamic responses, particularly VO2, HR, SBP, and RPP during the low-to-maximal exercise. The results showed that VO2, HR, SBP, and RPP increased in positively direct proportion to the increase in the exercise workload in TM and CE. The slope of the increasing line in the hemodynamic variables with the increased VO2 differed, however, between CE and TM.

Conventionally, in the graded exercise tolerance tests, VO2max differ most conspicuously in CE and TM. It has been reported that VO2max was higher in TM than in CE [15,16], and that the degree of difference varied from 6% to 25% [16]. These differences are considered attributable to the difference in examinees' ages and degrees of physical fitness, the type of exercise, and exercise test protocols. Consistent with the results of the previous studies, VO2max in this study were significantly lower in CE than in TM. As the TM test can most accurately measure VO2max and HRmax, the sensitivity in detecting myocardial ischemia is naturally higher in TM than in CE [17,18].

In this study, VO2 was first used as the criterion for the increasing exercise workload, and the degrees of HR, SBP, and RPP responses to the CE and TM exercise were ascertained. HR increased to the same degree as the increase of VO2 in CE and TM; whereas SBP and RPP increased considerably more in CE than in TM for most of the low- to high-intensity exercise loads. The slopes of the line of HR-VO2 with the gradual increase in the exercise workload in TM and CE were the same. The slopes of SBP and RPP with the increases in HR and VO2 were significantly higher in CE than in TM, though. As such, the increases in HR, SBP, and RPP had direct proportional relationships to the increase in VO2, and both SBP and RPP, but not HR, increased more in CE than in TM. Also, the SBP increase with the increase in HR was higher in CE than in TM. These results indicate that the BP response at a maximal exercise load is stronger in CE than in TM, which leads to higher RPP.

Balogun et al. [17] reported that the higher RPP in CE than in TM was attributable to the increased HR. In this study, however, the SBP increase was higher in CE than in TM when the same oxygen uptake and HR were used as criteria for the exercise load, and consequently, RPP also increased. This is a very interesting result that was not ascertained in the previous studies. A higher SBP in CE than in TM is observable in athletes. BP of endurance athletes during exercise can increase to 175/69 mmHg; whereas resistance athlete's BP can reach 480/350 mmHg at the maximum effort. Also, cycle athlete's BP increases to over 200 mmHg during cycling exercise [19-22]. Cycling and rowing are both dynamic and static exercises. Fagard [22] reported that in a large-scale study of 947 elite athletes, cycling and rowing increased the inside diameter of the left ventricle and the thickness of the myocardial wall the most. The high SBP during cycling and rowing is the main cause of the increased inside diameter of the left ventricle and the increased thickness of the myocardial wall [22]. In a recent study of women with sedentary lifestyles, both their SBP and diastolic blood pressure were higher in the CE test than in TM when 40% and 60% of the target HR were used [12]. That study explained the reason for the higher BP in CE as the increase in the blood flow resistance in the muscle in CE under a similar workload, the reduced stimulation of the vagus nerve, and the increased tension in the muscle with increased exercise intensity [23-25].

Generally, an exercise prescription is made with a lower minimal load, and it is recommended that the exercise load is 85% of the target HR, according to the Karvonen et al. [26]. When the data obtained from the TM test are applied to the Karvonen et al. [26], normal people can exercise in CE without any problem. However, patients with ischemic cardiovascular disease, exercise-induced hypertension, and aneurysm may be subject to a higher myocardial burden in CE. Therefore, for them to be able to exercise in TM, the exercise intensity should be determined based on the exercise load test performed in TM; and likewise, for them to be able to exercise in CE, the exercise prescription should be made based on the HR obtained from the exercise load test performed in CE. The correlation between the change in BP with increased HR in TM and CE should be identified in further studies; and based on such a correlation, an exercise prescription should be made using the formula for converting HR in TM to HR in CE, to obtain a similar myocardial burden.

Conventionally, the myocardial oxygen uptake (MVO2) has been an effective marker of the coronary circulation response in relation to the myocardial metabolic demand. MVO2 can be measured from SBP and HR (HR×SBP), and is generally defined as RPP or a double product [27,28]. It is reported that RPP is the most reliable marker of myocardial perfusion in patients with coronary arterial disease as well as in normal people. Many patients with chronic stable angina are likely to experience repetitive chest pain at the same RPP [5,29]. Moreover, the change in the ischemic ST segment occurs at certain RPPs, and the BP is likely to increase in patients with exercise-induced hypertension more significantly in CE than in TM. It was also reported that exercises that involve an increase in RPP without increasing HR to over 100 were the main reason for the rupture of aneurysm [4,29]. Beta-blockers, which are used to prevent such cardiovascular event and aneurysm, are known to be effective in reducing RPP [3,5,29]. Other research have also reported that cardiovascular disease patients, including hypertensive patients, showed a much more burden of RPP to the TM exercise at the intensity of 40% and 80% heart rate reserve (HRR) compared to the CE exercise at the same intensity of 40% and 80% HRR [30-32]. Thus, it was considered risky to apply data from TM to CE to make an exercise prescription for patients with ischemic cardiovascular disease, exercise-induced hypertension, or aneurysm. Although there has been no report that increased RPP due to increased SBP resulted in cardiovascular events more in CE than in TM at a maximal exercise load, clinical studies are required to ascertain this.

There was a limitation in this study. Even though the BP was measured by a single expertise in this study, the intra-rater reliability of BP measurements was not assessed. Therefore, some caution about measurement error on BP should be considered.

At the comparably given workloads ranging from the low to maximal intensity, the BP response is stronger in CE than in TM, which leads to higher RPP. Therefore, there is a possibility that CE could induce more burdens of workloads to cardiovascular system in humans. These findings could imply that people and patients with cardiovascular disease patients would do strenuous exercise at CE than in TM exercise.

ACKNOWLEDGMENTS

This study was supported by Korea National Sport University. We thank our colleagues for data collection and management at Korea National Sport University. We also thank all participants in this study.

Notes

No potential conflict of interest relevant to this article was reported.

References

1. American College of Sports Medicine. ACSM's guidelines for exercise testing and prescription 8th edth ed. Philadelphia: Lippincott Williams & Wilkins; 2010.
2. Ellestad MH. Stress testing: principles and practice 5th edth ed. New York: Oxford University Press; 2003.
3. Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM, et al. American College of Sports Medicine position stand. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc 2011;43:1334–1359. 21694556.
4. Fletcher GF, Balady GJ, Amsterdam EA, Chaitman B, Eckel R, Fleg J, et al. Exercise standards for testing and training: a statement for healthcare professionals from the American Heart Association. Circulation 2001;104:1694–1740. 11581152.
5. Mezzani A, Agostoni P, Cohen-Solal A, Corra U, Jegier A, Kouidi E, et al. Standards for the use of cardiopulmonary exercise testing for the functional evaluation of cardiac patients: a report from the Exercise Physiology Section of the European Association for Cardiovascular Prevention and Rehabilitation. Eur J Cardiovasc Prev Rehabil 2009;16:249–267. 19440156.
6. Myers J, Prakash M, Froelicher V, Do D, Partington S, Atwood JE. Exercise capacity and mortality among men referred for exercise testing. N Engl J Med 2002;346:793–801. 11893790.
7. Faulkner JA, Roberts DE, Elk RL, Conway J. Cardiovascular responses to submaximum and maximum effort cycling and running. J Appl Physiol 1971;30:457–461. 5572760.
8. Hermansen L, Ekblom B, Saltin B. Cardiac output during submaximal and maximal treadmill and bicycle exercise. J Appl Physiol 1970;29:82–86. 4912876.
9. Maeder M, Wolber T, Atefy R, Gadza M, Ammann P, Myers J, et al. Impact of the exercise mode on exercise capacity: bicycle testing revisited. Chest 2005;128:2804–2811. 16236958.
10. Pollock ML, Foster C, Schmidt D, Hellman C, Linnerud AC, Ward A. Comparative analysis of physiologic responses to three different maximal graded exercise test protocols in healthy women. Am Heart J 1982;103:363–373. 7064770.
11. Wicks JR, Sutton JR, Oldridge NB, Jones NL. Comparison of the electrocardiographic changes induced by maximam exercise testing with treadmill and cycle ergometer. Circulation 1978;57:1066–1070. 639226.
12. Reed J. Blood pressure responses of sedentary African American women during cycle and treadmill exercise. Ethn Dis 2007;17:59–64. 17274211.
13. Foster C, Gaeckle T, Braastad R, Schmidt DH, Port SC. First-pass radionuclide angiography during bicycle and treadmill exercise. J Nucl Cardiol 1995;2:485–490. 9420830.
14. Mundal R, Kjeldsen SE, Sandvik L, Erikssen G, Thaulow E, Erikssen J. Exercise blood pressure predicts cardiovascular mortality in middle-aged men. Hypertension 1994;24:56–62. 8021008.
15. Glassford RG, Baycroft GH, Sedgwick AW, Macnab RB. Comparison of maximal oxygen uptake values determined by predicted and actual methods. J Appl Physiol 1965;20:509–513. 5319996.
16. Myers J, Buchanan N, Walsh D, Kraemer M, McAuley P, Hamilton-Wessler M, et al. Comparison of the ramp versus standard exercise protocols. J Am Coll Cardiol 1991;17:1334–1342. 2016451.
17. Balogun MO, Sulyman BO, Akinwusi PO. A comparison of the cardiovascular responses to treadmill and bicycle ergometer exercise in healthy male Nigerians. Afr J Med Med Sci 1997;26:27–30. 10895224.
18. Yamakado T, Kasai A, Masuda T, Futagami Y, Kawasaki A, Zhang Y, et al. Exercise-induced coronary spasm: comparison of treadmill and bicycle exercise in patients with vasospastic angina. Coron Artery Dis 1996;7:819–822. 8993939.
19. MacDougall JD, Tuxen D, Sale DG, Moroz JR, Sutton JR. Arterial blood pressure response to heavy resistance exercise. J Appl Physiol 1985;58:785–790. 3980383.
20. Mitchell JH, Haskell WL, Raven PB. Classification of sports. Med Sci Sports Exerc 1994;26(10 Suppl):S242–S245. 7934746.
21. Palatini P, Mos L, Mormino P, Munari L, Del Torre M, Valle F, et al. Intra-arterial blood pressure monitoring in the evaluation of the hypertensive athlete. Eur Heart J 1990;11:348–354. 2332000.
22. Fagard R. Athlete's heart. Circulation 2001;103:E28–E29. 11171805.
23. Blomqvist CG, Lewis SF, Taylor WF, Graham RM. Similarity of the hemodynamic responses to static and dynamic exercise of small muscle groups. Circ Res 1981;48(6 Pt 2):I87–I92. 7226467.
24. Clarys JP, Cabri J, Gregor RJ. The muscle activity paradox during circular rhythmic leg movements. J Sports Sci 1988;6:229–237. 3221426.
25. Tulppo MP, Makikallio TH, Laukkanen RT, Huikuri HV. Differences in autonomic modulation of heart rate during arm and leg exercise. Clin Physiol 1999;19:294–299. 10451789.
26. Karvonen MJ, Kentala E, Mustala O. The effects of training on heart rate; a longitudinal study. Ann Med Exp Biol Fenn 1957;35:307–315. 13470504.
27. Nelson RR, Gobel FL, Jorgensen CR, Wang K, Wang Y, Taylor HL. Hemodynamic predictors of myocardial oxygen consumption during static and dynamic exercise. Circulation 1974;50:1179–1189. 4430113.
28. Gobel FL, Norstrom LA, Nelson RR, Jorgensen CR, Wang Y. The rate-pressure product as an index of myocardial oxygen consumption during exercise in patients with angina pectoris. Circulation 1978;57:549–556. 624164.
29. Gajulapalli RD, Aneja A, Rovner A. Cardiac stress testing for the diagnosis and management of coronary artery disease: a reference for the primary care physician. South Med J 2012;105:93–99. 22267098.
30. Kim YJ, Kim C, Ahn JK, Lim SW, Kim EK, Shin YO, et al. Comparison of myocardial oxygen uptake and blood pressure in myocardial infarction patients response to treadmill and bike exercise therapy. Korean J Sports Med 2002;20:15–21.
31. Kim C, Kim YJ. Comparison of myocardial oxygen demand and rate of perceived exertion according to the modes of exercise in ischemic heart disease. J Korean Acad Rehabil Med 2009;33:572–577.
32. Kim YJ, Kim CH. Cardiovascular and perceived exertion response to treadmill running and cycle ergometer exercise in reponsder and nonreponder acute coronary syndrome patients. J Life Sci 2008;18:1263–1270.

Article information Continued

Fig. 1

Hemodynamic differences between cycle ergometer (CE) and treadmill (TM) at the maximum level of workload (n=15). VO2max, maximum oxygen uptake; HRmax, maximum heart rate; SBPmax, maximum systolic blood pressure; RPPmax, maximum rate-pressure product.

Fig. 2

An example of hemodynamic patterns of the heart rate, systolic blood pressure (SBP) and rate-pressure product (RPP) according to the work rates on cycle ergometer (CE) and treadmill (TM) during the gradual exercise test (n=1). VO2, oxygen uptake.

Fig. 3

The slope differences between cycle ergometer (CE) and treadmill (TM) exercise during the graded exercise test. (A) Slope for heart rate (HR) to oxygen uptake (VO2): HR is the y-axis and VO2 is the x-axis. (B) Slope for systolic blood pressure (SBP) to VO2: SBP is the y-axis and VO2 is the x-axis. (C) Slope of rate-pressure product (RPP) to VO2: RPP is the y-axis and VO2 is the x-axis. (D) Slope for HR to SBP: HR is the y-axis and SBP is the x-axis. All values are mean±standard error.

Table 1

Characteristics of subjects (n=15)

Table 1

Values are mean±standard deviation (SD).

BMI, body mass index; HRrest, resting heart rate; SBPrest, systolic blood pressure at rest; DBPrest, diastolic blood pressure at rest; MAPrest, mean arterial blood pressure at rest; RPPrest, rate-pressure products at rest.