Serviços Personalizados
Journal
artigo
Indicadores
Compartilhar
Journal of Human Growth and Development
versão impressa ISSN 0104-1282versão On-line ISSN 2175-3598
J. Hum. Growth Dev. vol.30 no.2 São Paulo maio/ago. 2020
https://doi.org/10.7322/jhgd.v30.10374
ORIGINAL
The effects of aerobic exercise on biochemical parameters in individuals with CKD on hemodialysis: A longitudinal study
Fabiano Santana de OliveiraI, II, III; Mauro José de Deus MoraisI, II, III; Luiz Carlos de AbreuII, III; Andrés Ricardo Pérez-RieraII, III; Vitor E ValentiIV; Laércio da Silva PaivaV; Rodrigo Daminello RaimundoII, III
IUniversidade Federal do Acre (UFAC) - Rio Branco (AC), Brasil
IIPrograma de Pós-Graduação em Ciências da Saúde, Centro Universitário Saúde ABC, Santo André (SP), Brasil
IIILaboratório de Delineamento de Estudos e Escrita Científica, Centro Universitário Saúde ABC, Santo André (SP), Brasil
IVCentro de Estudos do Sistema Nervoso Autônomo (CESNA), Departamento de Fonoaudiologia, Faculdade de Filosofia e Ciências, Universidade Estadual Paulista (UNESP) - Marília (SP), Brasil
VDepartamento de Saúde da Coletividade, Laboratório de Epidemiologia e Análise de Dados, Centro Universitário Saúde ABC, Santo André (SP), Brasil
ABSTRACT
BACKGROUNG: Chronic kidney disease is directly related to cardiovascular disorders. Guided physical exercises significantly improve the adverse effects of dialytic treatment
OBJECTIVE: To analyze changes in biochemical parameters of subjects with chronic kidney disease undergoing moderate exercise during hemodialysis
METHODS: This is an experimental study composed of 54 subjects submitted to hemodialysis, split into a control group and a group with intervention. The experimental group underwent three weekly sessions of aerobic exercise, performed during hemodialysis sessions, with a duration of 30 minutes, for 12 weeks. The blood parameters of both groups were compared
RESULTS: Statistically significant differences were observed between pre (p=0.001) and post-exercise protocol for urea (p=0.006), calcium (p=0.001), alanine aminotransferase (p=0.020) and sodium (p=<0.001). In the control group, we observed significant differences for the calcium variable (p<0.001), alanine aminotransferase (p=0.024), hematocrit (p=0.015), calcium vs phosphorus (p=0.018), and sodium (p=0.023), before and after the period
CONCLUSION: Aerobic training during hemodialysis was able to maintain blood level stability in patients with chronic kidney disease, both during and at the end of the protocol, even considering increased blood flow. This trial is registered in the Brazilian registry of clinical Trials - number RBR-7354r6. : July 5, 2018 at 12:59 PM. : July 24, 2018 at 10:24 AM. Identification of the test - UTN Number: U1111-1216-8272
Keywords: Chronic kidney disease, hemodialysis, blood parameters, aerobic exercises.
Authors summary
Why was this study done?
Chronic kidney disease is one of the major health problems worldwide, because in addition to the disease, we have associated comorbidities increasing morbidity as well as mortality. Physical exercise is a great ally, having beneficial effects on patients with CKD, and with that, this study was done to analyze the effects of aerobic exercise on the biochemical parameters of patients with CKD during hemodialysis.
What did the researchers do and find?
The researchers worked with two groups of patients on hemodialysis (control group and intervention group). The intervention group underwent 3 months of aerobic exercise on a cycle ergometer for 30 min three times a week. We performed analyzes of the blood parameters of the two groups at three times: at the beginning before we started to apply the protocol. After 45 days of exercise and three months after the exercise intervention. When comparing the two groups, the researchers found no significant differences in the parameters evaluated.
What do these findings mean?
This discovery means that when comparing the two groups of the project after 3 months of aerobic exercise 3 times a week, we did not have changes in blood levels of urea, creatinine, calcium, phosphorus, pyruvic glutamic transaminase, glucose, potassium, hemoglobin, hematocrit, calcium , phosphorus and sodium in patients with chronic kidney disease. They demonstrate that patients with CKD on hemodialysis have great weakness in their health, because a safe aerobic exercise intervention was not able to significantly improve their blood parameters when compared to a group that did not undergo this intervention. More efficient mechanisms in the treatment of this disease should be investigated.
INTRODUCTION
The increase in chronic and degenerative diseases, such as chronic kidney disease (CKD), constitutes one of the most significant challenges of public health, as it is considered a worldwide social and economic problem, and associated to many co-morbidities, as well as to high expenses in public health1,2.
Subjects with CKD present less aerobic strength and functional capacity when compared to healthy inactive people3. Low cardiopulmonary and functional capacity are associated with higher mortality risk, hospital admissions, and co-morbidities in subjects in this population4,5. On the other hand, several types of exercises proved to improve tolerance to exercise and optimize physical activity in subjects undergoing hemodialysis (HD)6,7.
Regular physical exercise not only improves physical fitness, but also plays a beneficial and potentially therapeutic role in adults with CKD, through blood pressure control, a decrease in resting heart rate, and decrease in inflammatory cytokines8,9.
During exercise, the muscular system's energy demand increases oxygen consumption to a level 10 to 20 times higher than in rest10. This induces increased ROS flow in muscle fibers11. A response to the increase in ROS during physical training, especially when not exhaustive, is the induction of enzymatic Endogenous Antioxidant System (EAS) activation, which regulates enzymes such as Glutathione Peroxidase (GPx), Glutathione Reductase (GR) and Catalase (Cat) and Superoxide Reductase (SOD)12,13.
Subjects under HD undergo deconditioning and low tolerance to physical activities. Such elements seem to be related to muscle atrophy, uremic muscle dysfunction and malnutrition11,14. The presence of circulating toxins, the excess of body fluids, electrolytic disorders, nutrition alterations, inactivity and proinflammatory substance release, contribute directly or indirectly to the decrease of survival in subjects under HD15.
Qiu et al.16, conducted a meta-analysis about physical exercise in patients with Chronic Renal Failure; the researchers concluded the exercises programs improved body function and physical capacity in patients with hemodialysis. The benefits are in blood pressure and maximal oxygen consumption. When a decline of renal function occurs, there is a progression of disorders in mineral metabolism, deregulating plasma levels and tissue concentrations of calcium, phosphorus and potassium, which are common complications of CKD, a significant cause of morbidity and decrease in quality of life. There is increasing evidence suggesting that these disorders in mineral and bone metabolism are associated with an increased risk of cardiovascular calcification, morbidity and mortality.
Research that can investigate better ways to achieve positive results, with the intention of producing new knowledge and becoming products that better the health of the population. This could be a new diagnosis, new therapeutic treatments or aimed at promoting population health17,18. Corroborating the authors, the study followed a protocol of safe and reliable quality in its execution and data generation, providing reliable information for the health area.
We raised the hypothesis that aerobic exercise training during hemodialysis could improve biochemical markers in CKD subjects. In this sense, we aimed to analyze the changes in biochemical parameters of subjects with chronic kidney disease undergoing moderate exercise during hemodialysis.
METHODS
This study followed the guidelines of research involving humans. It was approved by the Ethics Committee in Research, of the Faculdade de Juazeiro do Norte, by number 1,962,092. All subjects that agreed to participate in the research signed an informed consent. This trial is registered in the Brazilian registry of clinical Trials - number RBR-7354r6.
It was an experimental study composed of 248 subjects from the Sistema Único de Saúde (SUS) in HD treatment for at least six months, 3 times a week, ambulatory, of both genders, with age ≥18 years. We selected a control group (n=27) and an intervention group (n=27) with a protocol of three weekly sessions of aerobic exercise, during the HD sessions, for 12 weeks. The research was conducted on 54 subjects (Figure 1). We performed studies on the blood parameters of all of them.
The study included patients with unstable angina, uncontrolled hypertension (systolic blood pressure, SBP: 200 mmHg and / or diastolic blood pressure, DBP: 100 mmHg), use of antiarrhythmic drugs, severe lung disease, acute systemic infection, severe renal osteodystrophy, neurological disorders, disabling musculoskeletal disorders and patients with lower limb access.
At the Nephrology unit, the HD sessions are held in four shifts from Monday to Saturday, divided into Monday, Wednesday and Friday and Tuesday, Thursday and Saturday, starting the first sessions at 5:00 p.m. and ending at 01:30 p.m., the following day. We initially selected 54 patients in two screening groups, in the first two shifts (5:00 to 9:30 and 10:00 to 14:00).
We selected, in the control group, patients with the same characteristics as the intervention group, taking into account the age range, time of treatment, presumed etiology of the disease, socio-demographic characteristics. The main findings of these characteristics are found in the Results section.
Program of aerobic exercise performed during HD
It is understood the importance of emphasizing the scientific method as a way to develop scientific research19. Following these guidelines, our protocol was directed according to Morais, where supervised aerobic training was performed in the initial two hours of hemodialysis, lasting 30 minutes. An ergometer cycle was used (Mini Bike Compact - E 14) with multifunction LCD: Scan, Time, ODO-RPM, distance, calories, speed, measuring (height x length x width: 49x41.5x34.5 m) to perform the aerobic exercise20.
The subjects performed the aerobic exercises in cyclic movements of lower limbs with 45 to 60% of maximum predicted heart rate (Maximum heart rate=220 - age)19. They were directed to have their arms extended as usual, at length reaching the hips, close to the body, arranged as pleasantly as possible. They started with the tolerated time and were encouraged to increase the intensity to achieve a set zone, and if possible even exceed their upper limit, until reaching the intervention time21.
In all the stages, the supplementary data of the subjects were collected through their clinical histories filled by the medical team of the hospital (age, gender, blood pressure, and heart rate measurement).
The criteria to interrupt the aerobic exercise included intense physical tiredness, chest pain, dizziness, pallor, fainting, tachycardia, hypotension and lower limbs fatigue, interdialytic weight gain greater than 5 kg, difficulty in vascular access and some significant complaint (pain, dyspnea, etc.) before or during training. In these cases, they were prevented from doing exercises on that day or while such alterations persisted, or according to the medical prescription of the sector. No patient was ill or had any undesirable symptoms that we had to discontinue the exercise with the cycle ergometer exercise.
The subjects blood parameters were evaluated monthly at the hospital of the clinics of Rio Branco, Acre, Brazil, in the department of Nephrology. In this way, during September, October, November and December, we took the blood results on the following parameters: Pre and post urea; Creatinine; Calcium; Phosphorus; pyruvic glutamic transaminase (GPT); Glucose; Potassium; Hemoglobin; Calcium, Phosphorus and Sodium. In this way, the subjects performed the exercises proposed in our work, and simultaneously, we collected the same blood parameters within their routine evaluations monthly.
Statistical analysis
The qualitative variables are presented by absolute and relative frequency and the quantitative variables are given by central tendency and variability measures, according to the normality test (Shapiro-Wilk test).
In order to evaluate the blood parameters before, during and after hemodialysis in the intervention group and in the control group, the Friedman test was used with post-test of pairwise comparison. Only the creatinine variable was compared before and after hemodialysis according to the group; this was made by Wilcoxon's test. A delta (Δ) was created by subtraction of the pre-HD time by the post HD time. To compare the deltas (Δ) of the blood parameters according to the type of treatment made, the Mann-Whitney test was used.
The magnitude of the difference between the groups of the biochemical parameters by the Cohen d test was calculated. The effect size was considered small (<0.5), medium (0.5 to 0.9) and large (> 0.9).
The level of significance adopted for this analysis was p<0.05. The statistical software used was Stata, version 11.0
RESULTS
A total of 54 patients were selected, 27 from the intervention group and 27 from the control group. The average age of the intervention group was 42+13 years, height of 1.59+0.08m, and weight was 64+15Kg. The control group, mean age was 46+15 years, with a mean height of 1.57+0.09m and weight average of 68+17Kg.
When analyzing Table 1, the intervention group, it shows an improvement in systolic blood pressure, from 160 mmHg to the beginning of the intervention to 150 mmHg three months later. In relation to diastolic blood pressure, the initial measure was 91 mmHg and after three months decreased to 90 mmHg remaining stable.
In the heart rate assessment, it started with an average of 86.47 beats per minute, ended with an average of 105.11 beats per minute, with an increase of 18.64 bpm after three months. Considering that heart rate average of 105 bpm is defined as a safe value and at the same time much better than what was started, we concluded that the patient's physical conditions improved at the end of the program. The control group, on the other hand, maintained an average of these same variables over the same three months, with no significant changes, as well as keeping the results very close to the intervention group (Table 1).
In the comparison of blood parameters before, during and after hemodialysis for the intervention group, statistically significant differences were observed for urea (p=0.001, before vs during and after HD; p=0.006, before vs during HD), calcium (p=0.001, before vs during and before vs after HD), pyruvic glutamic transaminase (GPT) (p=0.020, before vs during HD) and sodium (p=<0.001, before vs during and before vs after HD) (Table 2).
When the blood parameters were compared before, during and after HD in the control group, we also observed significant differences for the calcium variable (p<0.001, before vs during and before vs after HD), GPT (p=0.024, before vs after HD), hematocrit (p=0.015, during vs after HD), calcium vs phosphorus (p=0.018, before vs during HD) and sodium (p=0.023, before vs during HD) (Table 2).
When comparing blood parameters between trained and control groups, no statistically significant differences were observed between all parameters analyzed (p>0.05) (Table 3).
DISCUSSION
The number of chronic kidney failure treated with hemodialysis is continuously increasing, and most patients have reduced exercise and are at high risk for heart and vascular disease22. The findings of our study showed that a moderate-load aerobic exercise protocol in patients undergoing hemodialysis for 3 months on a cycle ergometer did not change the blood parameters of patients with CKD.
Zhenzhen Qiu et al.23 in their research, evaluated the effects of exercise on the health of patients with chronic renal failure. They show that physical activity benefits blood pressure among sick people and improves their maximal oxygen uptake. This can help patients with physical function and aerobic capacity, while offering additional benefits23. Our findings corroborate the author with regard to systolic blood pressure and heart rate, because at the end of the 3 months of intervention, although there was no statistically significant difference in systolic blood pressure (Table 3), the results showed better control. in this aspect. In heart rate, there was significant difference, showing positive results in physical aspect.
In this context, Fuhro et al.24 reported that intradialytic exercise does not have the additional effect of removing systemic solutes (i.e., urea and creatinine) nor does it alter C-reactive protein levels, corroborating our findings.
Musavian et al.25 compared the effects of active and passive intradialytic pedaling exercises in subjects undergoing HD. The authors reported no significant alterations in potassium, phosphorus and calcium serum levels at the end of the fourth and eighth weeks of passive intradialytic exercise. However, phosphorus levels were insignificantly reduced and calcium levels slightly increased. The efficacy of dialysis and urea uptake discretely decreased in the fourth week and mildly increased at the end of the eighth week of passive exercise. Nevertheless, these changes were not statistically significant26. The same results of the analyzed parameters were approximated of these same values without statistical difference.
Mohseni et al.27 examined the effect of intradialytic aerobic exercise on the efficacy of dialysis in subjects under HD. There was no significant difference in the reduction rate of basal urea between the two groups. The investigation showed that aerobic exercise could improve the efficacy of dialysis. This improvement could be due to the direct beneficial effects of aerobic exercise or the general effects of regular physical exercise. It seems that during exercise under HD, muscle blood flow increases and opens the capillary surface area that subsequently increased the flow of urea from the tissue into the vascular compartment28. Such growth would lead to an increase in serum clearance of urea and improvement in the efficacy of dialysis29. In the study published by Indralingam Vaithilingam et al.30 the rate of urea reduction (69% ± 0.02% versus 68% ± 0.07, 4 versus 5 hours) and the weekly removal of urea were not different between the control group and the intervention group. In our study we also found no difference in urea reduction rate between the two groups.
According to the Hermes Pardini Laboratory, the reference values to measure GPT by using the kinetic study through UV are: men - up to 50 U/L and women - up to 35 U/L. Some studies showed that subjects with CKD under HD could have lower serum levels of liver enzymes than those with a normal renal function for reasons that remain uncertain31,32.
In our study, we verified no difference of GTP levels between control and trained groups. These data corroborate the research of Block et al.33, in which subjects with CKD under HD had reduced serum levels of aminotransferases.
Small et al.31, showed that exercise training and lifestyle intervention in subjects with CKD in standard nephrology care did not produce significant changes in systemic biomarkers of oxidative stress. Our data indicated that aerobic exercise during HD did not avoid the impairment of blood parameters in CKD subjects. We should be careful when investigating HD for kidney diseases treatment.
The acute effects of exercise on CKD subjects were evaluated by Santana et al.32 which reported that a single aerobic exercise of moderate intensity of 30 minutes does not harm renal function in subjects with non-dialytic CKD, regardless of the stage of the disease, supporting the notion that exercise training could be safe in this disease.
In a systematic review and meta-analysis, Heiwe et al.6, verified whether physical exercise could affect health results in individuals with CKD. This review proposed that training with regular physical exercise is generally associated with better health outcomes in individuals with CKD.
CONCLUSION
There was no change during moderate aerobic exercise in the biochemical parameters during the three months intervention on blood levels of urea, creatinine, calcium, phosphorus, pyruvic glutamic transaminase, glucose, potassium, hemoglobin, hematocrit, calcium, phosphorus and sodium in patients with chronic kidney disease. The feasibility of using exercise in this population should be considered to control blood pressure, cardiac function and improvement of physical condition.
Declarations
Abbreviations
ADP - Adenosine Diphosphate
AMPK - AMP-activated protein kinase
AMP - Adenosine Monophosphate
ATP - Adenosine Triphosphate
Cat - Catalase
CKD - Chronic kidney disease
DOQI - Disease Outcomes Quality Initiative
EAS - Endogenous antioxidant systems
ROS - Reactive oxygen species
ERRα - Orphan Nuclear Receptor
GR - Glutathione Reductase
GPT - Glutamic Pyruvic Transaminase
GPx - Glutathione Peroxidase
HD - Hemodialysis
H2O2 - Hydrogen peroxide
IL-6 - Interleukin 6
Keap1- Kelch-like protein 1
LCD - Panel Reader
Nrf1 - Nuclear Respiratory Factor 1,
Nrf2 - Nuclear factor erythroid 2-related factor 2
ODO-RPM - Odometer with Rotation Per Minute
PGC-1α - Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-Alpha
PPAR - Peroxisome Proliferator-Activated Receptor
PTH - Parathormone
SIRT1 - Sirtuin 1
SOD - Superoxide Reductase
TNF-α - Tumor necrosis factor alpha
U / L - Unit per liter
Ethics approval and consent to participate
Not applicable
Consent for publication, availability of data and material, competitive interest, funding, authors' contributions are all included in the letter described below.
REFERENCES
1.Heiwe S, Clyne N, Dahlgren MA. Living with chronic renal failure: patients' experiences of their physical and functional capacity. Physiother Res Int . 2003;8(4):167-77. DOI: http://doi.org/10.1002/pri.287 [ Links ]
2.Locatelli F, Del Vecchio L, Pozzoni P. The importance of early detection of chronic kidney disease. Nephrol Dial Transplant. 2002;17(suppl 11):2-7. DOI: http://doi.org/10.1093/ndt/17.suppl_11.2 [ Links ]
3.Moinuddin I, Leehey DJ. A comparison of aerobic exercise and resistance training in patients with and without chronic kidney disease. Adv Chronic Kidney Dis. 2008;15(1):83-96. DOI: http://doi.org/10.1053/j.ackd.2007.10.004 [ Links ]
4.Sietsema KE, Amato A, Adler SG, Brass EP. Exercise capacity as a predictor of survival among ambulatory patients with end-stage renal disease. Kidney Int. 2004;65(2):719-24. DOI: http://doi.org/10.1111/j.1523-1755.2004.00411.x [ Links ]
5.Knight EL, Ofsthun N, Teng M, Lazarus JM, Curhan GC. The association between mental health, physical function, and hemodialysis mortality. Kidney Int. 2003;63(5):1843-51. DOI: http://doi.org/10.1046/j.1523-1755.2003.00931.x [ Links ]
6.Heiwe S, Jacobson SH. Exercise Training in Adults With CKD: A Systematic Review and Meta-analysis. Am J Kidney Dis. 2014;64(3):383-93. DOI: http://doi.org/10.1053/j.ajkd.2014.03.020 [ Links ]
7.Aoike DT, Baria F, Kamimura MA, Ammirati A, Mello MT, Cuppari L. Impact of home-based aerobic exercise on the physical capacity of overweight patients with chronic kidney disease. Int Urol Nephrol. 2015;47(2):359-67. DOI: http://doi.org/10.1007/s11255-014-0894-8 [ Links ]
8.Heiwe S, Jacobson SH. Exercise training for adults with chronic kidney disease. Cochrane Database Syst Rev. 2011;10(10):CD003236. DOI: http://doi.org/10.1002/14651858.CD003236.pub2 [ Links ]
9.Ploeger HE, Takken T, Greef MHG, Timmons BW. The effects of acute and chronic exercise on inflammatory markers in children and adults with a chronic inflammatory disease: a systematic review. Exerc Immunol Rev. 2009;15(1):6-41 [ Links ]
10.Powers SK, Jackson MJ. Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiol Rev. 2008;88(4):1243-76. DOI: http://doi.org/10.1152/physrev.00031.2007 [ Links ]
11.Roxo RS, Xavier VB, Miorin LA, Magalhaes AO, Sens YA, Alves VL. Impact of neuromuscular electrical stimulation on functional capacity of patients with chronic kidney disease on hemodialysis. J Bras Nefrol. 2016;38(3):344-50. DOI: http://dx.doi.org/10.5935/0101-2800.20160052 [ Links ]
12.Vargas-Mendoza N, Morales-Gonzalez A, Madrigal-Santillan EO, Madrigal-Bujaidar E, Alvarez-Gonzalez I, Garcia-Melo LF, et al. Antioxidant and Adaptative Response Mediated by Nrf2 during Physical Exercise. Antioxidants (Basel). 2019;8(6):196. DOI: http://dx.doi.org/10.3390/antiox8060196 [ Links ]
13.Cartee GD, Hepple RT, Bamman MM, Zierath JR. Exercise Promotes Healthy Aging of Skeletal Muscle. Cell Metab. 2016;23(6):1034-47. DOI: http://dx.doi.org/10.1016/j.cmet.2016.05.007 [ Links ]
14.Viana JL, Kosmadakis GC, Watson EL, Bevington A, Feehally J, Bishop NC, et al. Evidence for anti-inflammatory effects of exercise in CKD. J Am Soc Nephrol. 2014;25(9):2121-30. DOI: http://dx.doi.org/10.1681/ASN.2013070702 [ Links ]
15.Sethna CB, Salerno AE, McBride MG, Shults J, Paridon SM, Sharma N, et al. Cardiorespiratory fitness in pediatric renal transplant recipients. Transplantation. 2009;88(3):395. DOI: http://dx.doi.org/10.1097/TP.0b013e3181aed7d1 [ Links ]
16.Parsons TL, Toffelmire EB, King-VanVlack CE. The effect of an exercise program during hemodialysis on dialysis efficacy, blood pressure and quality of life in end-stage renal disease (ESRD) patients. Clin Nephrol. 2004;61(4):261-74. DOI: http://doi.org/10.5414/cnp61261 [ Links ]
17.Abreu LC, Pereira VX, Silva RPM, Macedo Jr H, Bezerra IMP. The right to scientific information: one of the main elements of the unified health system. J Hum Growth Dev. 2017;27(3):258-61. DOI: http://dx.doi.org/10.7322/jhgd.141485 [ Links ]
18.Bezerra IMP. Translational medicine and its contribution to public health. J Hum Growth Dev. 2017;27(1):6-9. DOI: http://dx.doi.org/10.7322/jhgd.127642 [ Links ]
19.Moraes SDTA. Scientific method and research in health: orientation for professional practice. J Hum Growth Dev. 2019;29(1):5-9. DOI: http://dx.doi.org/10.7322/jhgd.157742 [ Links ]
20.Morais MJD, Raimundo RD, Oliveira FS, Abreu LC, Bezerra IMP, Silva RPM, et al. Evaluation of the effects of aerobic training during hemodialysis on autonomic heart rate modulation in patients with chronic renal disease. Medicine (Baltimore). 2019;98(23):e15976. DOI: http://doi.org/10.1097/MD.0000000000015976 [ Links ]
21.Morais MJD, Abreu LC, Oliveira FS, Bezerra IMP, Raimundo RD, Silva RPM, et al. Is aerobic exercise training during hemodialysis a reliable intervention for autonomic dysfunction in individuals with chronic kidney disease? A prospective longitudinal clinical trial. J Multidiscip Healthc. 2019;12:711-8. DOI: http://doi.org/10.2147/JMDH.S202889 [ Links ]
22.Vecchi AF, Colucci P, Salerno F, Scalamogna A, Ponticelli C. Outcome of peritoneal dialysis in cirrhotic patients with chronic renal failure. Am J Kidney Dis. 2002;40(1):161-8. DOI: http://doi.org/10.1053/ajkd.2002.33925 [ Links ]
23.Qiu Z, Zheng K, Zhang H, Feng J, Wang L, Zhou H. Physical Exercise and Patients with Chronic Renal Failure: A Meta-Analysis. Biomed Res Int. 2017;2017:7191826. DOI: http://doi.org/10.1155/2017/7191826 [ Links ]
24.Fuhro MI, Dorneles GP, Andrade FP, Romao PRT, Peres A, Monteiro MB. Acute exercise during hemodialysis prevents the decrease in natural killer cells in patients with chronic kidney disease: a pilot study. Int Urol Nephrol. 2018;50(3):527-34. DOI: DOI: http://doi.org/10.1007/s11255-017-1747-z [ Links ]
25.Musavian AS, Soleimani A, Masoudi Alavi N, Baseri A, Savari F. Comparing the effects of active and passive intradialytic pedaling exercises on dialysis efficacy, electrolytes, hemoglobin, hematocrit, blood pressure and health-related quality of life. Nurs Midwifery Stud. 2015;4(1):e25922. DOI: http://doi.org/10.17795/nmsjournal25922 [ Links ]
26.Mohseni R, Emami Zeydi A, Ilali E, Adib-Hajbaghery M, Makhlough A. The effect of intradialytic aerobic exercise on dialysis efficacy in hemodialysis patients: a randomized controlled trial. Oman Med J. 2013;28(5):345-9. DOI: http://doi.org/10.5001/omj.2013.99 [ Links ]
27.Vaithilingam I, Polkinghorne KR, Atkins RC, Kerr PG. Time and exercise improve phosphate removal in hemodialysis patients. Am J Kidney Dis. 2004;43(1):85-9. DOI: http://doi.org/10.1053/j.ajkd.2003.09.016 [ Links ]
28.Dinkova-Kostova AT, Abramov AY. The emerging role of Nrf2 in mitochondrial function. Free Radic Biol Med. 2015;88(Pt B):179-88. DOI: http://doi.org/10.1016/j.freeradbiomed.2015.04.036 [ Links ]
29.Scarpulla RC. Nuclear control of respiratory chain expression by nuclear respiratory factors and PGC-1-related coactivator. Ann N Y Acad Sci. 2008;1147:321-34. DOI: http://doi.org/10.1196/annals.1427.006 [ Links ]
30.Sette LHBC, Lopes EPA. Liver enzymes serum levels in patients with chronic kidney disease on hemodialysis: a comprehensive review. Clinics (Sao Paulo, Brazil). 2014;69(4):271-8. DOI: http://doi.org/10.6061/clinics/2014(04)09 [ Links ]
31.Small DM, Beetham KS, Howden EJ, Briskey DR, Johnson DW, Isbel NM, et al. Effects of exercise and lifestyle intervention on oxidative stress in chronic kidney disease. Redox Rep. 2017;22(3):127-36. DOI: http://doi.org/10.1080/13510002.2016.1276314 [ Links ]
32.Santana DA, Poortmans JR, Dorea EL, Machado JBA, Fernandes AL, Sá-Pinto AL, et al. Acute exercise does not impair renal function in nondialysis chronic kidney disease patients regardless of disease stage. Am J Physiol Renal Physiol. 2017;313(2):F547-52. DOI: http://doi.org/10.1152/ajprenal.00131.2017 [ Links ]
33.Block GA, Hulbert-Shearon TE, Levin NW, Port FK. Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: a national study. Am J Kidney Dis. 1998;31(4):607-17. DOI: http://doi.org/10.1053/ajkd.1998.v31.pm9531176 [ Links ]
Correspondence:
profsantana@outlook.com
Manuscript received: September 2019
Manuscript accepted: January 2020
Version of record online: May 2020