Abstract
The primary objective of this study was to compare the effects on muscle metabolism of two types of aerobic training, with and without a load on the lower limbs, in adults with peripheral arterial disease (PAD). A simple blind randomized clinical trial was conducted using two groups: conventional aerobic (CG) and modified aerobic with a load on the lower limbs (MG). Both groups underwent training by walking three times a week over a 12-week period. The ratings of muscle metabolism were determined after a treadmill test with constant velocity and inclination concomitant with the use of near infrared spectroscopy (NIRS). Altogether 40 individuals with PAD (CG = 65.45 ± 10.60 and MG = 63.10 ± 10.54) were included in the study. After the intervention, in both groups, there was a reduction in the relative time to recovery (p = 0.002), an improvement in the re-oxygenation rate (p = 0.017), an increased time of resistance after reaching the lowest muscle oxygen saturation (StO2) (p < 0.001), an increase in the distance walked (p < 0.001), and an improvement of the walking economy relative to StO2 (p < 0.001). After 12 weeks of training, an improvement in the deoxygenation rate was observed in both groups (p = 0.002), but with a greater magnitude in the CG (p = 0.017). Only the CG presented an increase in time to reach the lowest StO2 on the treadmill after the intervention (p = 0.010). The traditional aerobic training was superior to the modified training in relation to the improvement of muscle metabolism in patients with PAD.
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Introduction
Individuals with peripheral arterial disease (PAD) have lower limb muscle ischemia due to imbalances between perfusion and metabolic demand1,2, with a direct impact on the ability to walk resulting in significant functional limitations3. The pathophysiological process of PAD is multifactorial and includes, in addition to arterial obstruction, endothelial dysfunction with poor blood flow distribution, mitochondrial dysfunction associated with worsening peripheral oxygen utilization capacity and increased inflammatory activity4.
Due to the musculoskeletal changes of PAD, such as loss of muscle mass and consequent reduction of the capacity to produce strength and resistance5,6,7,8, resistance muscle training has been suggested as a possible intervention in the treatment of individuals with the disease6,9. There is no consensus in the literature about the effects of this type of training in patients with PAD due to the heterogeneity of protocols used5,6,9,10,11,12. Therefore, to date, it is suggested that resistance training be a complementary intervention to traditional aerobic training. Physical exercise using walking, along with the use of shin weights in the lower limbs, may be an alternative way of imposing overload functionally, considering that individuals with PAD present with a significant limitation in performance during submaximal activities such as walking4. Although this training is a viable therapeutic option in the treatment of individuals with PAD, the effects of this type of program on muscle metabolism have not been described in the literature.
Using near-infrared light spectroscopy (NIRS) it is possible to verify, in real time, muscle ischemia triggered by ambulation or exercise by adjusting the oxyhemoglobin (HbO2), deoxyhemoglobin (HHb) and tissue saturation (StO2) variables13,14. The absolute values of oxygen saturation (StO2) at rest are similar between individuals with PAD and healthy individuals15. However, during physically active individuals with PAD reach significantly lower values of StO2, present a sudden fall in StO2 at the beginning of the exercise, and present a longer recovery time compared to healthy individuals13,14,15,16. The recovery time of StO2 in diabetic individuals with PAD that are unable to complete a five-minute treadmill test is significantly longer than the recovery time of individuals that are able to complete the same test15,17. The evaluation of individuals with PAD with the aid of NIRS makes it possible to simultaneously analyze the effects of limiting or compensatory factors on perfusion, muscle metabolism and functional capacity18. Given the alterations secondary to PAD, it is important to increase our knowledge of the chronic effects of the different types of training (aerobic and resisted muscle) on the muscular metabolic response.
Therefore, the primary objective of this study was to evaluate the effects of a modified training program on muscle metabolism, using walking concomitant with the use of lower limb overload in individuals with peripheral arterial disease, and compare it to traditional aerobic walking with respect to limiting symptoms of ischemia. The secondary objective was to compare the functional capacity response to the two types of training. The hypothesis of the present study was that patients with PAD who performed the modified aerobic with a load on the lower limbs would present greater gains in functional capacity, metabolism and muscular performance than subjects submitted to traditional aerobic walking training.
Materials and Methods
Study design
This study was approved by the Research Ethics Committee of Universidade Federal de Minas Gerais on February 15, 2016 (CAAE registration 51274515.4.0000.5149) and was registered at http://www.isrctn.com (ISRCTN 44928994). The project summary and consort check list are shown in supplementary information. All methods were performed in accordance with the relevant guidelines and regulations. All participants were duly informed about the study, including possible risks and benefits of the interventions, before signing the informed consent form. The present study is a randomized, single-blind clinical trial. It was not possible to blind the participants and the professionals responsible for the intervention due to the obvious difference between the two types of intervention. Therefore, only the evaluators were blinded and did not know the allocation of the individuals to the intervention groups. Participants were included in the study upon meeting the inclusion criteria. After selection and evaluation, the project coordinator referred the subjects to the professional responsible for the intervention, who, from a, block-generated sequential list, randomly allocated participants to one of two groups, the conventional aerobic group (CG) or the modified aerobic group concomitant with the use of lower limb (MG) overload. The project coordinator was responsible for generating the random allocation sequence, performed in blocks of four at www.randomization.com.
Sample
From February 2016 to March 2017 adults with PAD and intermittent claudication were enrolled in the study, from the Cardiology and Vascular Surgery Clinic, Clinical Hospital, Universidade Federal de Minas Gerais. Individuals with PAD were included in the study, regardless of sex, according to the following inclusion criteria: (1) presenting an ankle-brachial index (ABI) at rest of less than 0.9 and (2) no pain at rest. The exclusion criteria of the study were: (1) participation in a supervised exercise program in the last six months or (2) presence of diseases or complications that impeded training such as heart failure, unstable angina, arrhythmia, decompensated diabetes (capillary glycemia greater than 250 mg/dl), or signs of hemodynamic instability.
Measures
Two evaluations were performed, the first was prior to the intervention, and the second was at 12 weeks after supervised training (Fig. 1). In the evaluation, in order to characterize the sample, clinical data were collected by interview regarding the presence of diabetes mellitus, beta-blocker use, use of cilostazol, smoking, level of obstruction, presence of clinical signs of chronic venous insufficiency, body mass index, and resting ABI. The body mass index was calculated from the weight and height of the individuals measured using an anthropometric scale (Filizola Indústria Ltda, São Paulo-SP, Brazil). A handheld Doppler instrument (DV-2001, MEDPEJ®) were used to measure resting ABI on the left and right sides, obtained using the highest ankle systolic blood pressure (SBP) divided by the highest brachial SBP. The participant remained in the supine position for a period of 15 minutes before the measures begin. A specific upper limb cuff was used to assess the systolic pressures of both limbs. In both lower limbs, SBP was measured from the posterior tibial and dorsal arteries of the foot19. In addition, the treadmill test was performed at a constant velocity and slope (3.2 km/h and 10% inclination)20. NIRS (Artinis®, Portamon system, The Netherlands) was used to evaluate the changes of StO2 and HHb of the medial gastrocnemius muscle during the arterial occlusion maneuver, and during the treadmill test using Oxysoft software (Artinis®). After the ABI measurement, the NIRS sensors were positioned in the medial region of the gastrocnemius muscle at the level of the largest circumference, and fixed with plastic film and an elastic band18,21. The data were initially obtained at a frequency of 10 Hz. With the individual positioned in the dorsal decubitus position after initial stabilization of the measurement, the baseline value of StO2 was recorded, and the arterial occlusion maneuver was initiated. This maneuver was performed with a cuff positioned between the medial and distal third of the individual’s thigh. The cuff was inflated above 250 mmHg, but to a maximum of 280 mmHg22,23,24, and maintained for a period of five minutes, until the measures stabilized. This procedure worked as a physiological calibration, creating a functional scale that enabled a better comparison between different individuals, as the variables HbO2 and HHb were provided by the software in arbitrary units22,25. The NIRS device was maintained in the lower limb of the patient until recovery after the treadmill test.
To perform the treadmill test, the participant was instructed to walk for as long as possible until experiencing the moderate-to-maximum claudication symptoms. One minute of warm-up was carried out on the treadmill, in which there was a progressive increase of speed and inclination until 3.2 km/h speed and 10% incline was reached. One to two minutes of active recovery was maintained, in accordance with the tolerance of the individual, with a speed of 2.0 km/h and 0% inclination, from the moment in which the individual experienced the moderate-to-maximum claudication symptoms.
Study variables
The maximum distance traveled in the treadmill test at a constant velocity and inclination, and the variables obtained from the NIRS assessment during the arterial occlusion maneuver and the treadmill test were established as study variables. The variables obtained during the arterial occlusion maneuver were: recovery time of StO2 after occlusion, delta/variation of HHb during occlusion and delta/variation of StO2 during occlusion. The variables obtained from the treadmill test were: delta/variation of HHb, delta/variation of StO2, time to reach lower StO2, time to resistance after reaching lower StO2, relative time of recovery on the treadmill, deoxygenation rate, re-oxygenation rate, relative re-oxygenation rate, walking economy relative to HHb (meters/delta HHb), and walking economy related to StO2. The variables related to StO2 are described in Fig. 2.
Variables obtained by NIRS during the treadmill test for peripheral arterial disease. Adapted from Boezeman et al., 2016. A = StO2 value at rest; B = StO2 delta: StO2 variation during exercise; C = lower saturation value reached during exercise; D = time to reach the lowest saturation; Z = time to resistance after reaching lower StO2; X = time taken to recover baseline StO2 from the beginning of the test; Y = test duration time; X/Y = Relative recovery time of StO2 on the treadmill/; B/D = deoxygenation rate; B/X = re-oxygenation rate; B/(X/Y) = relative re-oxygenation rate during the treadmill test; distance traveled on the treadmill/B = walking economy relative to StO2.
Training protocols
The aerobic exercise training was performed three times per week, over a 12-week period by volunteers from both groups. The CG performed traditional training, while the MG performed training with progressive overload in the lower limbs. In both groups, the walking exercise was performed at an acceptable intensity until the moderate-to-maximum claudication symptoms occurred, allowing periods of recovery. As soon as there was a resolution of the claudication symptoms, a new walk was begun. The time required for the resolution of symptoms between each walk was disregarded in recording the total activity time, which should have been 30 minutes. Warm-ups and recovery were performed at the beginning and end of each walk, respectively, by both groups. The following parameters in all sessions were recorded: time to symptom onset, time to the onset of limiting pain, rest time required for symptoms to disappear, and total distance walked by the volunteer in each session. The training supervision was made by physical therapists. They were responsible for monitoring the hemodynamic response, progression of the protocol, as well as providing standardized instructions for the patient to reach moderate-to-maximum claudication symptoms during training.
Conventional aerobic training
The aerobic training of the CG was started with walking on the floor for 30 minutes. From the moment that the individual ceased to report a moderate-to-maximum claudication symptoms within 30 minutes, treadmill training on the treadmill without inclination, was started at the average velocity achieved during the last walking session on the floor. A progressive rise of 0.2 km/h in velocity was performed from the moment the individual ceased to report moderate-to-maximum claudication symptoms within 30 minutes on the treadmill.
Modified aerobic training
The aerobic walking training performed by the MG included a progressive overload on the lower limbs through the addition of ankle weights. Training was started on the floor, at first without a load on lower limbs. The loads were added gradually, according to the load progression protocol. From the time the individual reached the minimum time of 15 minutes of walking on the floor without experiencing a moderate-to-maximum claudication symptoms, ankle weights were added, progressively, adding 0.5 kilo in each lower limb up to 2 kilos and taking into account the time and the absence of a moderate-to-maximum claudication symptoms. From the moment that the individual reached the minimum time of 15 minutes with an overload of 2 kilos while walking on the ground without reach moderate-to-maximum claudication symptoms, training was started on the treadmill. The treadmill training started with the average speed reached on the floor, but without overload on the lower limbs. Weights were added at the ankles to increase the overload, progressively, evolving from 0.5 kg in each lower limb up to 2 kg, in the same way as in the floor training. A progressive rise of 0.2 km/h in the speed of the treadmill was followed, if the individual did not reach moderate-to-maximum claudication symptoms within 15 minutes after the addition of the load of 2 kilos.
Statistical analysis
The Anderson-Darling test was used to evaluate the normal distribution of the continuous variables. The descriptive analysis of the data and the results are expressed as mean ± standard deviation, or as absolute and relative frequencies.
The comparisons of the categorical variables, to characterize the groups, were performed using Fisher’s exact test (2 × 2 tables) or the Cramer’s V coefficient (asymmetric tables). To evaluate the differences between the groups (conventional and modified), the situation (pre- and post-intervention treadmill tests), and the interaction between the groups and the situation, the Linear Mixed Model was used. The dependent variables “groups” and “situation” were entered into the model as fixed effects, and the “subjects” was entered as a random effect. For the choice of the best model, the values for the maximum restricted likelihood (−2 restricted log likelihood) were used, the diagonal covariance structure was used for the repeated measures, and the first order autoregressive structure was used for random effects. Compared to the intention-to-treat analysis, this method provides better estimates for lost data and addresses individual differences more adequately26,27. An alpha value of 5% was set for statistical significance. The data were analyzed using the statistical software Statistical Package for the Social Sciences - (SPSS, Inc., USA, version 15.0).
Sample size calculation
Initially, the sample size was calculated considering the variable total distance on the treadmill test as the most important variable for the analysis28. From previous studies of individuals with PAD with similar characteristics to the subjects allocated for this study29, the sample size calculated was 70 participants per group, setting a power of 80% and an alpha error of 5%. In a second moment, from a pilot study with 12 individuals in each group, the sample size was recalculated to represent the smallest size of effect for the estimation of the n sample size. To perform the calculation, an alpha error of 5% and a power of 0.80 were set, and the size of the effect of the ANOVA (f) was estimated by the equation: \((f=\sqrt{\frac{S{Q}_{A}}{S{Q}_{e}}})\), where SQA = the sum of the squares of the respective source of variation and SQE = the sum of the squares of the errors30,31. From the sample size calculation, 18 individuals were required per group. Considering the potential subject losses, 10% was added to the n calculated, totaling 20 individuals per group.
Results
Table 1 presents the clinical characteristics of the population sample included in the study. Initially, 54 volunteers with PAD and claudication, were eligible for the study. After applying the inclusion and exclusion criteria, 40 individuals were included. Over the course of the study, eight total participants abandoned treatment, comprising four from each group. The flowchart of the study is shown in Fig. 1. Figure 3 shows the data from one participant exemplifying the mean changes of the NIRS variables during and after the arterial occlusion maneuver.
Data from one participant exemplifying the mean changes of the NIRS variables during (A to B) and after (after B) the arterial occlusion maneuver. In the left pannel (I) the red line represents oxyhemoglobin (HbO2); the blue line represents deoxyhemoglobin (HHb) and the green line represents the total hemoglobin (tHb). In the right pannel (II) green line represents tissue saturation (StO2).
No difference in exercise intensity, characterized by the mean percentage of predicted maximum heart rate for age that was reached by both groups during the sessions (73.77 ± 12.1% in the conventional group and 72.42 ± 10.52% in the modified group, p = 0.740), was observed in the present study. Adherence to treatment was not different between the two groups (91.17 ± 6.39% in the conventional group and 89.05 ± 10.85% in the modified group; p = 0.894). There was no difference in ABI between the groups, or between the pre- and post-intervention situations (CG pre-intervention: right ABI 0.63 ± 0.17 and left ABI 0.63 ± 0.17; CG post-intervention: right ABI 0.65 ± 0.2 and left ABI 0.68 ± 0.16; GM pre-intervention: right ABI 0.62 ± 0.18 and left ABI 0.63 ± 0.18, and post-intervention: right ABI 0.63 ± 0.16 and left ABI 0.62 ± 0.15; right ABI effect group p = 0.531 and effect situation p = 0.070; left ABI effect group p = 0.689 and effect situation p = 0.101).
The mean changes of the NIRS variables during the occlusion maneuver and during the pre- and post-intervention treadmill tests are described in Tables 2 and 3, respectively. In Table 3, one can observe significant differences between the groups in the training response time to reach the lower StO2 on the treadmill, and in the deoxygenation rate. An improvement in the functional capacity of the individuals of both groups was observed on the treadmill test after the intervention (CG pre-intervention 183.98 meters 95% CI 115.44–293.19, and CG post-intervention 1669.64 meters 95% CI 1210.41–2303.09; GM pre-intervention 173.95 meters 95% CI 111.78–270.68, and GM post-intervention 1154.48 meters 95% CI 690.97–1928.84; effect group p = 0.385, effect situation p < 0.001, and effect interaction p = 0.444).
Discussion
The present study is innovative as an assessment of the effects on muscle metabolism of overload training on the lower limbs compared to conventional walking, by means of adjustments of the NIRS. Our hypothesis was that patients with PAD who performed the modified aerobic with a load on the lower limbs would present greater gains in functional capacity, metabolism and muscular performance than subjects submitted to traditional aerobic walking training. Although differences in the muscular metabolic adaptive mechanisms were observed between the two groups, as verified by changes of the NIRS variables, both interventions resulted in improved walking capacity as evaluated by the treadmill test. A high adherence rate was observed, which was not different between the two intervention modalities. Despite the difference in body mass index (BMI) between the groups, both groups were in the overweight range. We believe that the possible clinical repercussions of being overweight were similar between the groups, so no adjustment was made in the statistical analysis for the variable BMI.
In both groups, there was a reduction of the relative recovery time on the treadmill, characterized by the ratio between the time required to return to the baseline StO2 and the total test time. Therefore, after the training the individuals took relatively less time to recover the baseline StO2 value as they walked longer. Our study corroborates the results of two other studies that verified the reduction of time required to recover StO2 after treadmill testing, following 12 weeks of training32,33. According to Beckit et al. (2012), the improvement in StO2 recovery after physical training reflects the combination of improvement in metabolic economy and muscle oxidative capacity. This suggests that exercise helps to reverse the metabolic myopathy acquired by individuals with PAD33. In addition, after the training, in both groups there was an increase in the time of resistance after reaching the lowest StO2. This finding indicates that after the intervention, the subjects were able to maintain walking exercise for a longer period of time, despite the level of muscle ischemia. The improvement of resistance after reaching the lowest StO2 reinforces the theory that training optimizes the transport and use of oxygen in patients with PAD34.
Both groups displayed improvement in the re-oxygenation rate relative to the total time for the treadmill test, characterized by the ratio between the StO2 variation during the test and the relative recovery time on the treadmill. Recovery after exercise reflects how much the oxygen supply exceeds the oxygen demand for muscle recovery16. As no change was observed in the variation of the StO2 after the intervention, the improvement in the rate of re-oxygenation is the result of a reduction in the time required for recovery of StO2 relative to the total test time. That is, for the same variation of StO2 during the test, the individual was able to recover faster, even having walked for longer after the intervention. The improvement in the re-oxygenation rate and the relative time of recovery suggest a probable optimization of both muscular oxidative capacity and vascular function34.
An improvement of the deoxygenation rate after the treatment was also observed in both groups. However, the conventional group presented a significantly higher result than the modified group. The deoxygenation rate is characterized by the ratio between the variation of StO2 during the test and the time to reach the lowest StO2 value. The improvement observed with regard to this variable implies a reduction in the velocity of deoxygenation induced by the exercise, indicating a probable improvement of the muscular oxidative capacity33. Although both groups showed an improvement in the deoxygenation rate, only the conventional group showed an increase in the time to reach the lowest StO2 on the treadmill after the intervention. This may have contributed to a higher magnitude of response in relation to the observed deoxygenation rate in the conventional group. Published studies have shown that both traditional walking and pole stride walking increased both the time required to achieve the lowest StO2 during the treadmill test and the walking capacity of individuals with PAD35,36. Another study also observed an increase in the time required to achieve the lowest StO2 during treadmill tests, in a group undergoing supervised walking training, and in a group that underwent unsupervised walking. This finding indicated that improvement in microvascular function as desaturation of oxygen-induced exercise was slower after training32. Tew et al.37 performed training with upper limb cycle ergometers in individuals with PAD, and also observed an increase in the time required to reach the lowest StO2 during exercise. Ischemia caused by the reduction of exercise-induced microvascular oxygenation is known to potentially cause the release of nitric oxide from the endothelium, therefore, improving vascular function38,39. The results found by these authors37, demonstrated an improvement in global vascular function, characterized by an improvement in the availability of oxygen to the lower limb during exercise that was detected by NIRS, even with training carried out using the upper limbs. Although in our study, the modified group did not show an improvement in the time to reach the lowest saturation on the treadmill, this group displayed an improvement in the distance. This result suggests that other adaptive mechanisms resulted in improved functional capacity in the modified group.
An improvement in walking economy relative to StO2, defined as the ratio between the number of meters traveled for each unit of StO2 fall, was observed in both groups. After the intervention the subjects were able to walk greater distances for each unit of StO2 fall. Although no statistically significant difference was detected between the groups after treatment, a clinically significant difference was observed in favor of the conventional group, with an increase in the walking economy by 11.09-fold versus a 5.75-fold increase in the modified group. The differences in the adaptations generated by the two types of interventions may justify the clinically significant difference in walking economy between the two groups.
The difference in the use of cilostazol between conventional and aerobic groups in this study may be considered a limitation. A recent meta-analysis found that cilostazol presents a negligible benefit in improving the maximum distance walked by individuals with PAD when compared to usual care. However, only exercise training was found to have a positive effect on the ability to walk40, Therefore, cilostazol, when compared with the usual care, has no positive effect on walking ability in individuals with PAD40. Although a decreased need for cilostazol was observed in the conventional group, the use of the drug did not influence adaptations to training, especially because there was no difference in walking ability among the groups.
The possible adverse effects expected from modified aerobic training were fatigue and muscular pain secondary to adding weights to the legs of people with PAD. However, none of these adverse effects were reported during the study demonstrating the viability of this type of training for PAD individuals. A pilot study was previously conducted to assess the viability and the progression of the aerobic training protocol with a load on the lower limbs in adults with PAD.
Conventional training resulted in greater optimization of the muscular oxidative capacity and vascular function in this study, since the CG presented an increase in the time to reach the lower StO2. Additionally, CG showed a greater improvement in the deoxygenation rate and a clinically significant difference in walking economy compared to MG. Although the two types of interventions resulted in different adaptive responses to training, as detected by NIRS, no difference in walking ability between the groups was observed. Despite different adaptive responses, the two groups showed significant functional improvement. The results of this study suggest that training has the potential to optimize microvascular perfusion and oxidative capacity, further increasing the availability of oxygen in the active fibers and resulting in functional improvement. The results of the present study are in agreement with previous studies performed on individuals with PAD, in which there was an increase in extraction capacity, muscle oxygen availability and functional capacity after training sessions18,32,34,35,36,37. These results, together with our data, suggest a relationship between muscle metabolic improvement and endothelial function, and clinical and functional improvement observed in individuals with PAD34.
Conclusion
The present study demonstrated that traditional aerobic training was superior to modified walk training concomitant with overload in the lower limbs with respect to improvement of muscle metabolism. The conventional training resulted in a greater optimization of muscular oxidative capacity and vascular function in patients with PAD. However, the differences in the adaptive mechanisms did not result in differences in the walking ability among the groups after the intervention. The findings of this study broaden the understanding of the adjustments produced by two different types of exercise, and their utility in the optimization of rehabilitation programs for individuals with PAD, and for future studies.
References
McDermott, M. M. Lower extremity manifestations of peripheral artery disease: the pathophysiologic and functional implications of leg ischemia. Circ Res 116, 1540–1550, https://doi.org/10.1161/CIRCRESAHA.114.303517 (2015).
Hamburg, N. M. & Creager, M. A. Pathophysiology of Intermittent Claudication in Peripheral Artery Disease. Circ J 81, 281–289, https://doi.org/10.1253/circj.CJ-16-1286 (2017).
Hiatt, W. R., Armstrong, E. J., Larson, C. J. & Brass, E. P. Pathogenesis of the limb manifestations and exercise limitations in peripheral artery disease. Circ Res 116, 1527–1539, https://doi.org/10.1161/CIRCRESAHA.116.303566 (2015).
Hamburg, N. M. & Balady, G. J. Exercise rehabilitation in peripheral artery disease: functional impact and mechanisms of benefits. Circulation 123, 87–97, https://doi.org/10.1161/CIRCULATIONAHA.109.881888 (2011).
Hiatt, W. R., Wolfel, E. E., Meier, R. H. & Regensteiner, J. G. Superiority of treadmill walking exercise versus strength training for patients with peripheral arterial disease. Implications for the mechanism of the training response. Circulation 90, 1866–1874 (1994).
McGuigan, M. R. et al. Resistance training in patients with peripheral arterial disease: effects on myosin isoforms, fiber type distribution, and capillary supply to skeletal muscle. J Gerontol A Biol Sci Med Sci 56, B302–310 (2001).
McDermott, M. M. et al. Leg strength in peripheral arterial disease: associations with disease severity and lower-extremity performance. Journal of vascular surgery 39, 523–530 (2004).
Atkins, L. M. & Gardner, A. W. The relationship between lower extremity functional strength and severity of peripheral arterial disease. Angiology 55, 347–355, https://doi.org/10.1177/000331970405500401 (2004).
McDermott, M. M. et al. Treadmill exercise and resistance training in patients with peripheral arterial disease with and without intermittent claudication: a randomized controlled trial. JAMA 301, 165–174, https://doi.org/10.1001/jama.2008.962 (2009).
Regensteiner, J. G., Steiner, J. F. & Hiatt, W. R. Exercise training improves functional status in patients with peripheral arterial disease. J Vasc Surg 23, 104–115 (1996).
Ritti-Dias, R. M. et al. Strength training increases walking tolerance in intermittent claudication patients: randomized trial. J Vasc Surg 51, 89–95, https://doi.org/10.1016/j.jvs.2009.07.118 (2010).
Parmenter, B. J., Raymond, J., Dinnen, P., Lusby, R. J. & Fiatarone Singh, M. A. High-intensity progressive resistance training improves flat-ground walking in older adults with symptomatic peripheral arterial disease. J Am Geriatr Soc 61, 1964–1970, https://doi.org/10.1111/jgs.12500 (2013).
Boezeman, R. P., Moll, F. L., Ünlü, Ç. & de Vries, J. P. Systematic review of clinical applications of monitoring muscle tissue oxygenation with near-infrared spectroscopy in vascular disease. Microvasc Res 104, 11–22, https://doi.org/10.1016/j.mvr.2015.11.004 (2016).
Kooijman, H. M., Hopman, M. T., Colier, W. N., van der Vliet, J. A. & Oeseburg, B. Near infrared spectroscopy for noninvasive assessment of claudication. J Surg Res 72, 1–7, https://doi.org/10.1006/jsre.1997.5164 (1997).
Comerota, A. J., Throm, R. C., Kelly, P. & Jaff, M. Tissue (muscle) oxygen saturation (StO2): a new measure of symptomatic lower-extremity arterial disease. Journal of vascular surgery 38, 724–729 (2003).
Kemp, G. J. et al. Mitochondrial function and oxygen supply in normal and in chronically ischemic muscle: a combined 31P magnetic resonance spectroscopy and near infrared spectroscopy study in vivo. J Vasc Surg 34, 1103–1110, https://doi.org/10.1067/mva.2001.117152 (2001).
Komiyama, T., Shigematsu, H., Yasuhara, H. & Muto, T. Near-infrared spectroscopy grades the severity of intermittent claudication in diabetics more accurately than ankle pressure measurement. Br J Surg 87, 459–466, https://doi.org/10.1046/j.1365-2168.2000.01381.x (2000).
Manfredini, F. et al. A dynamic objective evaluation of peripheral arterial disease by near-infrared spectroscopy. Eur J Vasc Endovasc Surg 38, 441–448, https://doi.org/10.1016/j.ejvs.2009.06.011 (2009).
Aboyans, V. et al. Measurement and interpretation of the ankle-brachial index: a scientific statement from the American Heart Association. Circulation 126, 2890–2909 (2012).
Chaudhry, H., Holland, A. & Dormandy, J. Comparison of graded versus constant treadmill test protocols for quantifying intermittent claudication. Vasc Med 2, 93–97, https://doi.org/10.1177/1358863X9700200204 (1997).
Quaresima, V. et al. Calf and shin muscle oxygenation patterns and femoral artery blood flow during dynamic plantar flexion exercise in humans. Eur J Appl Physiol 84, 387–394, https://doi.org/10.1007/s004210100390 (2001).
McLay, K. M., Nederveen, J. P., Pogliaghi, S., Paterson, D. H. & Murias, J. M. Repeatability of vascular responsiveness measures derived from near‐infrared spectroscopy. Physiological reports 4, e12772 (2016).
Crenshaw, A. G., Elcadi, G. H., Hellstrom, F. & Mathiassen, S. E. Reliability of near-infrared spectroscopy for measuring forearm and shoulder oxygenation in healthy males and females. European journal of applied physiology 112(2703–2715%@), 1439–6319 (2012).
Martin, D. S., Levett, D. Z. H., Bezemer, R., Montgomery, H. E. & Grocott, A. T. C. X. E. R. G. M. P. W. The use of skeletal muscle near infrared spectroscopy and a vascular occlusion test at high altitude. High altitude medicine & biology 14(256–262%@), 1527–0297 (2013).
Ferrari, M., Muthalib, M. & Quaresima, V. The use of near-infrared spectroscopy in understanding skeletal muscle physiology: recent developments. Philos Trans A Math Phys Eng Sci 369, 4577–4590, https://doi.org/10.1098/rsta.2011.0230 (2011).
Press, R. A mixed model approach for intent-to-treat analysis in longitudinal clinical trials with missing values (2009).
Detry, M. A. & Ma, Y. Analyzing Repeated Measurements Using Mixed Models. JAMA 315, 407–408, https://doi.org/10.1001/jama.2015.19394 (2016).
Triola, M. F. In Introdução à estatística: atualização da tecnologia (Ltc, 2014).
da Cunha-Filho, I. T. et al. The reliability of walking tests in people with claudication. Am J Phys Med Rehabil 86, 574–582, https://doi.org/10.1097/PHM.0b013e31806de721 (2007).
Hedeker, D., Gibbons, R. D. & Waternaux, C. Sample size estimation for longitudinal designs with attrition: comparing time-related contrasts between two groups. Journal of Educational and Behavioral Statistics 24, 70–93 (1999).
Portney, L. G. & Watkins, M. P. Foundations of clinical research: applications to practice. (FA Davis, 2015).
Gardner, A. W., Parker, D. E., Montgomery, P. S. & Blevins, S. M. Step-monitored home exercise improves ambulation, vascular function, and inflammation in symptomatic patients with peripheral artery disease: a randomized controlled trial. J Am Heart Assoc 3, e001107, https://doi.org/10.1161/JAHA.114.001107 (2014).
Beckitt, T. A., Day, J., Morgan, M. & Lamont, P. M. Calf muscle oxygen saturation and the effects of supervised exercise training for intermittent claudication. J Vasc Surg 56, 470–475, https://doi.org/10.1016/j.jvs.2011.11.140 (2012).
Fiogbé, E., de Vassimon-Barroso, V. & de Medeiros Takahashi, A. C. Exercise training in older adults, what effects on muscle oxygenation? A systematic review. Arch Gerontol Geriatr 71, 89–98, https://doi.org/10.1016/j.archger.2017.03.001 (2017).
Collins, E. G. et al. Comparison of walking with poles and traditional walking for peripheral arterial disease rehabilitation. J Cardiopulm Rehabil Prev 32, 210–218, https://doi.org/10.1097/HCR.0b013e31825828f4 (2012).
Collins, E. G. et al. The effects of walking or walking-with-poles training on tissue oxygenation in patients with peripheral arterial disease. International journal of vascular medicine 2012 (2012).
Tew, G., Nawaz, S., Zwierska, I. & Saxton, J. M. Limb-specific and cross-transfer effects of arm-crank exercise training in patients with symptomatic peripheral arterial disease. Clin Sci (Lond) 117, 405–413, https://doi.org/10.1042/CS20080688 (2009).
Pohl, U. & Busse, R. Hypoxia stimulates release of endothelium-derived relaxant factor. American Journal of Physiology-Heart and Circulatory Physiology 256, H1595–H1600 (1989).
Brendle, D. C., Joseph, L. J., Corretti, M. C., Gardner, A. W. & Katzel, L. I. Effects of exercise rehabilitation on endothelial reactivity in older patients with peripheral arterial disease. The American journal of cardiology 87, 324–329 (2001).
Vemulapalli, S. et al. Comparative Effectiveness of Medical Therapy, Supervised Exercise, and Revascularization for Patients With Intermittent Claudication: A Network Meta-analysis. Clin Cardiol 38, 378–386, https://doi.org/10.1002/clc.22406 (2015).
Acknowledgements
This study received financial support from Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Pró-Reitoria de Pesquisa da Universidade Federal de Minas Gerais.
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D.P. conceived and designed research; G.S. analyzed data; D.M. was responsible for implementation of the study; D.P. and D.M. drafted manuscript; R.B. revised manuscript; D.P., D.M., G.S. and R.B. approved final version of manuscript.
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Monteiro, D.P., Ribeiro-Samora, G.A., Britto, R.R. et al. Effects of modified aerobic training on muscle metabolism in individuals with peripheral arterial disease: a randomized clinical trial. Sci Rep 9, 15966 (2019). https://doi.org/10.1038/s41598-019-52428-7
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DOI: https://doi.org/10.1038/s41598-019-52428-7