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Resistance exercise: an effective strategy to reverse muscle wasting in hemodialysis patients?
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PMID:  25163460     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Muscle wasting is a common complication afflicting maintenance hemodialysis (HD) patients, and it is associated with decreased muscle function, exercise performance, physical function, and quality of life. Meanwhile, numerous epidemiologic studies have consistently shown that greater muscle mass (ascertained by body anthropometry surrogates, body composition tests such as dual x-ray absorptiometry, and/or serum creatinine in patients with little to no residual kidney function) is associated with increased survival in this population. The pathophysiology of muscle wasting in HD patients is complex and may be caused by poor dietary intake, catabolic effects of dialysis therapy, hormonal alterations (e.g., decreased levels or resistance to anabolic hormones, increased levels of catabolic hormones), inflammation, metabolic acidosis, and concurrent comorbidities. Muscle disuse resulting from low physical activity is an important yet under-appreciated risk factor for muscle wasting. Intra-dialytic resistance exercise training has been suggested as a potential strategy to correct and/or prevent this complication in HD patients, but prior studies examining this exercise modality as an anabolic intervention have shown mixed results. In a recently published 12-week randomized controlled trial of a novel intra-dialytic progressive resistance exercise training (PRET) program vs. control therapy conducted in HD and non-HD patients, PRET resulted in increased muscle volume and strength in both groups. At this time, further study is needed to determine if anabolic improvements imparted by resistance exercise translates into improved physical function and quality of life, decreased hospitalization and mortality risk, and greater cost-effectiveness in HD patients.
Connie M Rhee; Kamyar Kalantar-Zadeh
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Type:  Journal Article     Date:  2014-08-28
Journal Detail:
Title:  Journal of cachexia, sarcopenia and muscle     Volume:  5     ISSN:  2190-5991     ISO Abbreviation:  J Cachexia Sarcopenia Muscle     Publication Date:  2014 Sep 
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Created Date:  2014-09-10     Completed Date:  2014-09-10     Revised Date:  2014-09-16    
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Nlm Unique ID:  101552883     Medline TA:  J Cachexia Sarcopenia Muscle     Country:  Germany    
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Languages:  eng     Pagination:  177-80     Citation Subset:  -    
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Journal ID (nlm-ta): J Cachexia Sarcopenia Muscle
Journal ID (iso-abbrev): J Cachexia Sarcopenia Muscle
ISSN: 2190-5991
ISSN: 2190-6009
Publisher: Springer Berlin Heidelberg, Berlin/Heidelberg
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© Springer-Verlag Berlin Heidelberg 2014
Received Day: 8 Month: 8 Year: 2014
Accepted Day: 8 Month: 8 Year: 2014
Electronic publication date: Day: 28 Month: 8 Year: 2014
Print publication date: Month: 9 Year: 2014
Volume: 5 Issue: 3
First Page: 177 Last Page: 180
PubMed Id: 25163460
ID: 4159495
Publisher Id: 160
DOI: 10.1007/s13539-014-0160-z

Resistance exercise: an effective strategy to reverse muscle wasting in hemodialysis patients?
Connie M. RheeAff1Aff2 Address: (714) 456-5142
Kamyar Kalantar-ZadehAff1Aff2Aff3 Address: (714) 456-5142
Harold Simmons Center for Chronic Disease Research and Epidemiology, Division of Nephrology and Hypertension, University of California Irvine Medicine Center, 101 The City Drive South, City Tower, Orange, CA 92868-3217 USA
Los Angeles Biomedical Research Institute, Harbor-UCLA, Torrance, CA USA
Veterans Affairs Long Beach Health Care System, Long Beach, CA USA

Main text

Approximately 20 to 50 % of maintenance hemodialysis (HD) patients suffer from protein-energy wasting (PEW), a condition of decreased body protein and fat mass that potently predicts morbidity and mortality in this population [13]. Muscle wasting is a key component of PEW, and it adversely affects multiple patient-centered outcomes including muscle function, exercise performance, physical function, and quality of life (QOL) [4, 5].

Numerous epidemiologic studies have also consistently shown that reduced muscle mass is associated with decreased survival in end-stage renal disease patients, including those receiving HD, peritoneal dialysis, or kidney transplantation [614]. While various body anthropometry surrogates (e.g., mid-arm muscle circumference [9]) and sophisticated equations have been utilized to estimate muscle mass in these studies [10], serum creatinine has been found to be a reliable marker of muscle mass in dialysis patients with little to no residual kidney function [13]. Indeed, a number of studies have shown that lower serum creatinine levels in HD patients are associated with increased death risk [6, 7, 11]. Recent data also suggest that decreased muscle strength may be an even more potent mortality predictor than muscle mass [15].

Given its high prevalence and dire sequelae, considerable study has been made to understand the underlying etiologies of muscle wasting in HD patients, in order to identify strategies that correct and/or prevent this complication (Fig. 1). The pathophysiology of muscle wasting and weakness appears to be complex and multifactorial and may be attributed to one or more of (1) insufficient nutritional intake; (2) catabolic effects of dialysis therapy; (3) hormonal aberrations including low levels or increased resistance to anabolic hormones (e.g., testosterone, growth hormone, insulin-like growth factor-1 [IGF-1]), increased levels of catabolic hormones (e.g., cortisol), and possible thyroid hormone deficiency; (4) chronic inflammation; (5) metabolic acidosis; and (6) concurrent comorbidities (e.g., diabetic gastroparesis) [1, 4, 16, 17].

Muscle disuse due to reduced physical activity (defined as “any bodily movement produced by contraction of skeletal muscle that increases energy expenditure above a basal level” [18]) is another important yet relatively under-appreciated risk factor for muscle wasting in HD patients [19]. Epidemiologic data show that physical activity levels in HD patients are exceedingly low. Among 1,547 ambulatory dialysis patients in the Comprehensive Dialysis Study, physical activity scores ascertained by the Human Activity Profile were below the fifth percentile of healthy individuals based on age and sex norms [20]. Similarly, among 134 patients in the Dialysis Outcomes and Practice Patterns Study, 64 % of patients had sedentary or low physical activity levels [21]. While the 2005 Kidney Disease Outcomes Quality Initiative Clinical Practice Guidelines on Cardiovascular Disease in Dialysis Patients recommend that nephrology and dialysis staff routinely counsel dialysis patients on increasing their physical activity levels [22], survey data has shown that less than one-third of nephrologists routinely recommend exercise (a form of physical activity that is “planned, structured, repetitive, and purposive in the sense that the improvement or maintenance of one or more components of physical fitness is the objective” [23, 24]) [25]. This may in part relate to providers’ uncertainties regarding the benefits of exercise upon short- and long-term outcomes in HD patients as well as its optimal modality, prescription, and associated risks in this population.

A number of studies have examined various modalities of exercise training in dialysis patients over the past three decades [26]. While most studies have focused on aerobic exercise, which primarily improves cardio-respiratory endurance and fitness, there have been fewer studies of resistance exercise, which promotes muscle growth, mass, and strength; has been shown to be an effective anabolic intervention in elderly patients and other chronic disease populations [27]; and is theoretically a more optimal exercise modality in enhancing physical function [4, 26, 28]. Furthermore, there has been particular interest in studying resistance exercise during or around the time of dialysis treatment, which is thought to enhance compliance and to counter-act muscle wasting at a time when catabolism is at its peak [1]. In a sentinel study by Johansen et al., among 79 HD patients randomized to a 2 × 2 factorial trial of moderate-intensity intra-dialytic resistance exercise training and anabolic steroid administration (nandrolone decanoate) for 12 weeks, exercise resulted in increased quadriceps muscle cross-sectional area measured by MRI, increased strength, and improved self-reported physical function [29]. However, resistance exercise did not increase lean body mass detected by dual-energy x-ray absorptiometry nor improve physical performance (e.g., walk test, stair climb, chair rise). Shortly thereafter, an elegant study conducted by Kopple et al. showed that, among 80 patients randomized to intra-dialytic strength/resistance training, endurance training, strength/resistance + endurance training, vs. no exercise training, those assigned to resistance or endurance training experienced increases in muscle mRNA, muscle IGF-1 protein, and lean body mass ascertained by anthropometric measurements [30]. However, other randomized controlled trials of moderate- to high-intensity resistance training alone, or in combination with intra-dialytic nutritional supplementation, have not shown improvements in muscle cross-sectional area nor lean body mass and have been inconsistent with respect to effects upon muscle strength [3133]. Hence, the utility of intra-dialytic resistance exercise as an anabolic intervention in HD patients has remained unclear.

A recent study by Kirkman et al. published in the Journal of Cachexia, Sarcopenia, and Muscle entitled “Anabolic Exercise in Haemodialysis Patients: A Randomized Controlled Pilot Study” has sought to address this knowledge gap by examining the impact of a novel intra-dialytic progressive resistance exercise training (PRET) program on muscle volume, strength, and physical function in HD patients as well as in non-HD healthy patients during university visits [19]. In this single-blind controlled study, 23 HD and 9 non-HD patients were randomized to PRET, which consisted of thrice-weekly high-intensity leg press exercises (three sets of eight to ten repetitions at 80 % of their predicted one-repetition maximum, which is the maximum weight that can be lifted one time with proper technique), vs. control (SHAM) therapy, which consisted of low-intensity lower body stretching activities using ultra-light resistance bands. An important innovation of this study was to incorporate an incremental increase in the weekly training load/volume in the PRET arm of the trial. After a 12-week interventional period, PRET resulted in a significant increase in (1) the primary outcome of thigh muscle volume ascertained by MRI and (2) the secondary outcome of knee extensor strength measured by isometric dynamometer in both HD and non-HD patients. Furthermore, patients randomized to SHAM therapy, particularly those in the HD group, experienced clinically significant amounts of muscle volume loss.

However, PRET did not enhance HD patients’ (3) performance in physical function tests (e.g., sit-to-stand, get-up-and-go, walk test) or (4) self-reported QOL ascertained by the Short Form-36, although improvements in non-HD patients were observed. This stands in contrast to prior studies in the elderly, those with other catabolic states, and dialysis patients in whom similar interventions have resulted in improved physical function [27, 34]. This study’s discrepant findings may have been due to (1) selection of particular physical function assessment tests that have a high degree of variability, are subject to a ceiling effect, or have limited ability to capture improvements in activities of daily living as compared to other physical function instruments and metrics (i.e., self-reported physical function) [29]; (2) type 2 error due to the small sample size of the pilot study; or (3) true absence of effect on physical function and QOL.

Several important contributions made by Kirkman et al.’s study should be noted. First, their incorporation of a graded increase in weekly training load/volume in the study arm may be necessary to promote an adequate anabolic response in HD patients, and the absence of this intervention in prior studies of resistance training may in part explain the inconsistencies across these collective data [19, 2933]. Second, while earlier studies of intra-dialytic resistance have employed combination anabolic interventions (i.e., anabolic hormone administration [29], intra-dialytic nutritional supplementation [33]) given concerns that exercise both stimulates muscle protein synthesis and breakdown, the findings of the Kirkman et al. study suggest that PRET alone can augment muscle volume and strength. Third, while there may be theoretical concerns related to the risk of exercise in HD patients (e.g., particularly musculoskeletal injury, cardiac ischemia, and sudden cardiac death as well as exercise-related hypo- and hypertension, electrolyte abnormalities, and hypoglycemia [26, 28]), the low frequency and rather mild nature of adverse events observed in HD patients assigned to the PRET arm provides further reassurance that resistance exercise is safe in this population. However, it is of our opinion that HD patients with underlying history or risk factors for cardiopulmonary disease and related comorbidities should undergo exercise testing prior to the initiation of a resistance exercise training program.

Taken together, these data corroborate that resistance exercise training administered at incrementally higher levels is an effective and safe anabolic intervention in HD patients. At this time, further study is needed to determine if these short-term augmentations in muscle volume and strength translate into improved physical function, QOL, hospitalization and mortality risk, and cost-effectiveness.

The authors certify that they comply with the ethical guidelines for authorship and publishing of the Journal of Cachexia, Sarcopenia, and Muscle (von Haehling S, Morley JE, Coats AJS, Anker SD. Ethical guidelines for authorship and publishing in the Journal of Cachexia, Sarcopenia, and Muscle. J Cachexia Sarcopenia Muscle. 2010;1:7–8.)

Conflict of interest

Connie M. Rhee and Kamyar Kalantar-Zadeh declare that they have no conflict of interests related to the present submission.

Funding source

The authors are supported by the research grants from the NIH/NIDDK including K24-DK091419 (KKZ), R01-DK078106 (KKZ), and philanthropist grants from Mr. Harold Simmons and Mr. Louis Chang.

1.. Dong J,Ikizler TA. New insights into the role of anabolic interventions in dialysis patients with protein energy wastingCurr Opin Nephrol HypertensYear: 2009184697510.1097/MNH.0b013e328331489d19713839
2.. Fouque D,Kalantar-Zadeh K,Kopple J,Cano N,Chauveau P,Cuppari L,et al. A proposed nomenclature and diagnostic criteria for protein-energy wasting in acute and chronic kidney diseaseKidney IntYear: 200873391810.1038/
3.. Kalantar-Zadeh K,Rhee C,Sim JJ,Stenvinkel P,Anker SD,Kovesdy CP. Why cachexia kills: examining the causality of poor outcomes in wasting conditionsJ Cachexia Sarcopenia MuscleYear: 20134899410.1007/s13539-013-0111-023749718
4.. Ikizler TA. Exercise as an anabolic intervention in patients with end-stage renal diseaseJ Ren Nutr Off J Counc Ren Nutr Natl Kidney FoundYear: 20112152610.1053/j.jrn.2010.10.012
5.. Johansen KL,Shubert T,Doyle J,Soher B,Sakkas GK,Kent-Braun JA. Muscle atrophy in patients receiving hemodialysis: effects on muscle strength, muscle quality, and physical functionKidney IntYear: 200363291710.1046/j.1523-1755.2003.00704.x12472795
6.. Kalantar-Zadeh K,Streja E,Kovesdy CP,Oreopoulos A,Noori N,Jing J,et al. The obesity paradox and mortality associated with surrogates of body size and muscle mass in patients receiving hemodialysisMayo Clin ProcYear: 201085991100110.4065/mcp.2010.033621037042
7.. Kalantar-Zadeh K,Streja E,Molnar MZ,Lukowsky LR,Krishnan M,Kovesdy CP,et al. Mortality prediction by surrogates of body composition: an examination of the obesity paradox in hemodialysis patients using composite ranking score analysisAm J EpidemiolYear: 201217579380310.1093/aje/kwr38422427612
8.. Molnar MZ,Streja E,Kovesdy CP,Bunnapradist S,Sampaio MS,Jing J,et al. Associations of body mass index and weight loss with mortality in transplant-waitlisted maintenance hemodialysis patientsAm J Transplant Off J AmSoc Transplant Ame SocTransplant SurgYear: 2011117253610.1111/j.1600-6143.2011.03468.x
9.. Noori N,Kopple JD,Kovesdy CP,Feroze U,Sim JJ,Murali SB,et al. Mid-arm muscle circumference and quality of life and survival in maintenance hemodialysis patientsClin J Am Soc NephrolYear: 2010522586810.2215/CJN.0208031020947789
10.. Noori N,Kovesdy CP,Bross R,Lee M,Oreopoulos A,Benner D,et al. Novel equations to estimate lean body mass in maintenance hemodialysis patientsAm J Kidney Dis Off J Natl Kidney FoundYear: 201157130910.1053/j.ajkd.2010.10.003
11.. Park J,Jin DC,Molnar MZ,Dukkipati R,Kim YL,Jing J,et al. Mortality predictability of body size and muscle mass surrogates in Asian vs white and African American hemodialysis patientsMayo Clin ProcYear: 2013884798610.1016/j.mayocp.2013.01.02523562348
12.. Park J,Mehrotra R,Rhee CM,Molnar MZ,Lukowsky LR,Patel SS,et al. Serum creatinine level, a surrogate of muscle mass, predicts mortality in peritoneal dialysis patientsNephrol Dial Transplant Off Publ Eur Dial Transplant Assoc Eur Ren AssocYear: 201328214655
13.. Patel SS,Molnar MZ,Tayek JA,Ix JH,Noori N,Benner D,et al. Serum creatinine as a marker of muscle mass in chronic kidney disease: results of a cross-sectional study and review of literatureJ Cachexia Sarcopenia MuscleYear: 20134192910.1007/s13539-012-0079-122777757
14.. Streja E,Molnar MZ,Kovesdy CP,Bunnapradist S,Jing J,Nissenson AR,et al. Associations of pretransplant weight and muscle mass with mortality in renal transplant recipientsClin J Am Soc NephrolYear: 2011614637310.2215/CJN.0913101021415312
15.. Isoyama N, Qureshi AR, Avesani CM, Lindholm B, Barany P, Heimburger O, et al. Comparative associations of muscle mass and muscle strength with mortality in dialysis patients. Clinical Journal of the American Society of Nephrology: CJASN. 2014. Epub 2014/07/31.
16.. Rhee CM,Alexander EK,Bhan I,Brunelli SM. Hypothyroidism and mortality among dialysis patientsClin J Am Soc NephrolYear: 2013859360110.2215/CJN.0692071223258793
17.. Rhee CM, Brent GA, Kovesdy CP, Soldin OP, Nguyen D, Budoff MJ, et al. Thyroid functional disease: an under-recognized cardiovascular risk factor in kidney disease patients. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association—European Renal Association. 2014. Epub 2014/02/28.
18.. Painter P,Marcus RL. Assessing physical function and physical activity in patients with CKDClin J Am Soc NephrolYear: 201388617210.2215/CJN.0659071223220421
19.. Kirkman DL, Mullins P, Junglee NA, Kumwenda M, Jibani MM, Macdonald JH. Anabolic exercise in haemodialysis patients: a randomised controlled pilot study. J Cachexia Sarcopenia Muscle. 2014. Epub 2014/04/09.
20.. Johansen KL,Chertow GM,Kutner NG,Dalrymple LS,Grimes BA,Kaysen GA. Low level of self-reported physical activity in ambulatory patients new to dialysisKidney IntYear: 20107811647010.1038/ki.2010.31220811334
21.. Avesani CM,Trolonge S,Deleaval P,Baria F,Mafra D,Faxen-Irving G,et al. Physical activity and energy expenditure in haemodialysis patients: an international surveyNephrol Dial Transplant Off Publ Eur Dial Transplant Assoc Eur Ren AssocYear: 20122724304
22.. K/DOQI clinical practice guidelines for cardiovascular disease in dialysis patients. American journal of kidney diseases: the official journal of the National Kidney Foundation. 2005; 45(4 Suppl 3):S1–153.
23.. Physical Activity Guidelines Advisory Committee: Physical Activity Guidelines Advisory Committee Report, 2008, Washington, DC, U.S. Department of Health and Human Services, 2008.
24.. Caspersen CJ,Powell KE,Christenson GM. Physical activity, exercise, and physical fitness: definitions and distinctions for health-related researchPublic Health RepYear: 1985100126313920711
25.. Johansen KL,Sakkas GK,Doyle J,Shubert T,Dudley RA. Exercise counseling practices among nephrologists caring for patients on dialysisAm J Kidney Dis Off J Natl Kidney FoundYear: 200341171810.1053/ajkd.2003.50001
26.. Johansen KL. Exercise in the end-stage renal disease populationJ Am Soc NephrolYear: 20071818455410.1681/ASN.200701000917442789
27.. Lemmey AB,Marcora SM,Chester K,Wilson S,Casanova F,Maddison PJ. Effects of high-intensity resistance training in patients with rheumatoid arthritis: a randomized controlled trialArthritis RheumYear: 20096117263410.1002/art.2489119950325
28.. Johansen KL,Painter P. Exercise in individuals with CKDAm J Kidney Dis Off J Natl Kidney FoundYear: 2012591263410.1053/j.ajkd.2011.10.008
29.. Johansen KL,Painter PL,Sakkas GK,Gordon P,Doyle J,Shubert T. Effects of resistance exercise training and nandrolone decanoate on body composition and muscle function among patients who receive hemodialysis: a randomized, controlled trialJ Am Soc NephrolYear: 20061723071410.1681/ASN.200601003416825332
30.. Kopple JD,Wang H,Casaburi R,Fournier M,Lewis MI,Taylor W,et al. Exercise in maintenance hemodialysis patients induces transcriptional changes in genes favoring anabolic muscleJ Am Soc NephrolYear: 20071829758610.1681/ASN.200607079417942969
31.. Cheema B,Abas H,Smith B,O’Sullivan A,Chan M,Patwardhan A,et al. Randomized controlled trial of intradialytic resistance training to target muscle wasting in ESRD: the Progressive Exercise for Anabolism in Kidney Disease (PEAK) studyAm J Kidney Dis Off J Natl Kidney FoundYear: 2007505748410.1053/j.ajkd.2007.07.005
32.. Cheema B,Abas H,Smith B,O’Sullivan A,Chan M,Patwardhan A,et al. Progressive exercise for anabolism in kidney disease (PEAK): a randomized, controlled trial of resistance training during hemodialysisJ Am Soc NephrolYear: 200718159460110.1681/ASN.200612132917409306
33.. Dong J,Sundell MB,Pupim LB,Wu P,Shintani A,Ikizler TA. The effect of resistance exercise to augment long-term benefits of intradialytic oral nutritional supplementation in chronic hemodialysis patientsJ Ren Nutr Off J Counc Ren Nutr Natl Kidney FoundYear: 2011211495910.1053/j.jrn.2010.03.004
34.. Headley S,Germain M,Mailloux P,Mulhern J,Ashworth B,Burris J,et al. Resistance training improves strength and functional measures in patients with end-stage renal diseaseAm J Kidney Dis Off J Natl Kidney FoundYear: 2002403556410.1053/ajkd.2002.34520


[Figure ID: Fig1]
Fig. 1 

Risk factors and sequelae of muscle wasting in hemodialysis patients

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