Figures
Abstract
Introduction
Congenital myopathies (CM) often affect contractile proteins of the sarcomere, which could render patients susceptible to exercise-induced muscle damage. We investigated if exercise is safe and beneficial in patients with CM.
Methods
Patients exercised on a stationary bike for 30 minutes, three times weekly, for 10 weeks at 70% of their maximal oxygen uptake (VO2max). Creatine kinase (CK) was monitored as a marker of muscle damage. VO2max, functional tests, and questionnaires evaluated efficacy.
Results
Sixteen patients with CM were included in a controlled study. VO2max increased by 14% (range, 6–25%; 95% CI 7–20; p < 0.001) in the seven patients who completed training, and tended to decrease in a non-intervention group (n = 7; change -3.5%; range, -11–3%, p = 0.083). CK levels were normal and remained stable during training. Baseline Fatigue Severity Scale scores were high, 4.9 (SE 1.9), and tended to decrease (to 4.4 (SE 1.7); p = 0.08) with training. Nine patients dropped out of the training program. Fatigue was the major single reason.
Conclusions
Ten weeks of endurance training is safe and improves fitness in patients with congenital myopathies. The training did not cause sarcomeric injury, even though sarcomeric function is affected by the genetic abnormalities in most patients with CM. Severe fatigue, which characterizes patients with CM, is a limiting factor for initiating training in CM, but tends to improve in those who train.
Trial Registration
The Regional Committee on Health Research Ethics of the Capital Region of Denmark H-2-2013-066 and ClinicalTrials.gov H2-2013-066
Citation: Hedermann G, Vissing CR, Heje K, Preisler N, Witting N, Vissing J (2016) Aerobic Training in Patients with Congenital Myopathy. PLoS ONE 11(1): e0146036. https://doi.org/10.1371/journal.pone.0146036
Editor: Jonatan R. Ruiz, University of Granada, SPAIN
Received: June 8, 2015; Accepted: December 11, 2015; Published: January 11, 2016
Copyright: © 2016 Hedermann et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: Funding provided by Direktør Jacob Madsen & Hustru Olga Madsen foundation. Grant no. 5289. No website. Received by GH. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: NP reports received research support, honoraria, and travel funding from Genzyme Corporation. JV reports received research support, honoraria, and travel funding from Genzyme Corporation. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials.
Abbreviations: CM, congenital myopathy; CK, creatine kinase; FSS, Fatigue Severity Scale; FRSTST, five repetition sit-to-stand test; MRC, Medical Research Council; T14SST, timed 14-step-stair-test; VO2max, maximal oxygen uptake; 6MWT, 6-minute walk test
Introduction
Congenital myopathies (CM) are genetically and histologically heterogeneous disorders caused by mutations in genes that often encode sarcomeric proteins. Traditionally, CM is divided into three subtypes defined by histopathological findings on muscle biopsy: nemaline, central core and centronuclear myopathy. Genetic studies have shown that this division cannot stand alone. Thus, each subtype, defined by histological findings, can be caused by mutations in multiple genes, and mutation in a single gene can result in multiple phenotypic and histological presentations. Despite the variations, these patients typically present with a non-progressive early-onset muscle weakness. Some patients have involvement of extraocular and/or facial musculature. Creatine kinase (CK) levels are in the normal range or slightly elevated [1–3]. Fatigue is a prominent symptom in patients with CM [4].
The majority of patients with neuromuscular disorders live a sedentary life [5]. It has become evident from several studies, conducted in the last decade, that aerobic training is beneficial for several muscle diseases [6–10]. The effect of training has never been investigated in patients with CM, and due to the involvement of contractile proteins of the sarcomere, it could be hypothesized that training is deleterious in these conditions. The aim for this study was to investigate the effect on maximal oxygen uptake (VO2max) of 10 weeks of aerobic training in a cohort of patients with CM.
Materials and Methods
Subjects
To be eligible for inclusion in the study, patients had to be over the age of 18 and had to have confirmed pathogenic mutation(s) in genes, which are known to cause CM (see Table 1).
Patients 1–7 completed the training program. Patients 8–16 dropped out of the training program. Patients 5–11 participated in the non-intervention group. Patients 2 and 11 had bilateral foot drop requiring braces. Patient 3 took Alendronat 70 mg weekly to prevent osteoporosis, and Patient 7 used BiPAP at night. Patient 8 took Budesonid inhalations for asthma.
Additionally, patients had to be able to cycle for 30 minutes to be included in the study. Patients with competing medical conditions such as contractures, arthritis, heart- and lung diseases that could interfere with interpretation of exercise testing in the eyes of the investigator, and patients that performed more than one hour of aerobic training weekly were excluded.
Patients were recruited from a cohort of 33 genetically confirmed cases of CM older than 18 years. Eleven of the patients did not fulfil inclusion criteria, and 6 patients were not interested in participating. The remaining 16 patients were included in the study (Fig 1A and Table 1)
(A) 16 patients with CM were included in the study. Four patients from the 1st training group completed the training program. A non-intervention group of seven CM patients were tested twice, 10 weeks apart, before they participated in the training program (2nd training group). Only 3 patients from the non-intervention group completed the subsequent training program. In total, nine patients dropped out of the training program. (B) VO2max before and after 10 weeks of aerobic training in seven CM patients with an improvement corresponding to 215 ml O2 · min-1 (CI 121–308 ml O2 · min-1, * p = 0.001) (left bars). VO2max before and after 10 weeks of normal daily living in seven patients with CM (right bars). Black bars represent values before, and gray bars represent values after. The change seen in the intervention group was significant compared to the change in the non-intervention group (mixed Anova, p < 0.001). (C) Maximal workload before and after 10 weeks of aerobic training in seven CM patients who improved Wmax by 18 W (CI 11–24 W, ** p = < 0.001) (left bars). Wmax before and after 10 weeks of normal daily living in seven CM patients (right bars). Black bars represent values before, and gray bars represent values after. The change seen in the intervention group was significant compared to the change in the non-intervention group (mixed Anova, p < 0.001). (D) Dots represent plasma CK levels at week 0, 3 and 10 from the seven CM patients who finished the training program. All values are within the normal range or slightly elevated when corrected for age and gender. VO2max: maximal oxygen uptake; CM: congenital myopathy; Wmax: maximal workload; CK: creatine kinase.
Study design
The study setup dictated a non-blinded design, but was controlled by a parallel non-intervention group that served as a control for the trained group (see Fig 1A, flowchart). On inclusion, all patients accepted to conduct a 10-week training program. Patients were divided in two groups; one started the training program and the other started a period of unchanged daily living (non-intervention group). After 10 weeks of unchanged daily living, the patients in the non-intervention group started their training program. The allocation to training first or later was not randomized, because of time constraints for a number of participants. All patients had to complete a test day before and after the 10-week intervention or non-intervention periods. Based on effect (a change of 18.6% or more) and variation (SD = 0.15) in VO2max responses to aerobic training for 10–12 weeks in other muscle diseases [6–9], and assuming a chance of type 1 error of 0.05 and a type 2 error of 0.19, the needed number in the training group to complete training is 7 persons.
Test days
Patients performed a peak exercise test on a cycle ergometer and three functional tests; a 6-minute walk test (6MWT), a five repetition sit-to-stand test (FRSTST), and a timed 14-step-stair-test (T14SST) (tests described in Table 2 and [10]). At inclusion, muscle strength was evaluated by a modified 10-step Medical Research Council (MRC) scale. Muscle strength has been measured by handheld dynamometry in previous studies on 10–12 weeks of cycle training in other muscle diseases [11–12]. No significant outcome was seen with this type of exercise, so muscle strength was not evaluated with a dynamometer in this study. Forced vital capacity (FVC) was measured by spirometry in all patients.
6MWT: 6-minute walk test (m: distance in meters). FRSTST: five times repetitive sit-to-stand test (s: seconds), the patient was asked to rise and sit from a chair five times as fast as possible. T14SSTn: timed 14-step-stair-test (normal speed), the patient had to climb and decline 14 steps at their normal speed. T14SSTq: timed 14-step-stair-test (quick), the patient had to climb and decline 14 steps as fast as possible. FSS: fatigue severity scale. ND: not determined. Values are mean ± standard deviation. P-values in the right column are calculated by a mixed Anova test, no significant difference was found between the improvements seen in the intervention group compared with the improvements in the non-intervention group.
Patients completed four questions from the SF-36 questionnaire concerning fatigue on all test days.
Furthermore, they completed the Fatigue Severity Scale (FSS) at baseline and after the training. FSS rates fatigue perceived in the preceding week. FSS score ≥ 4 indicates abnormal fatigue, and a score ≥ 5 indicates severe fatigue [4].
Plasma creatine kinase (CK) levels were measured on test days and after three weeks of training as a marker of exercise-induced muscle damage.
Peak exercise testing
Testing was performed on an electronically braked Lode Excalibur Sport cycle ergometer. The person who measured VO2max was not blinded, but the tests were carried out systematically after standard guidelines in the laboratory. Prior to testing, patients were fitted with a heart rate monitor, 3-lead ECG electrodes and a facial mask. Pulmonary gas exchange was measured with breath-by-breath indirect calorimetry (Quark CPET, Cosmed Srl, Milan, Italy). Workload was increased incrementally. The patients were verbally encouraged to keep exercising for as long as possible. The test was terminated when the patients were unable to maintain their pedaling cadence (10% drop in rotation per minute (RPM) in 20 s). The VO2max was a mean of the period of 20 seconds where they performed the highest VO2max.
Home-based, pulse-monitored training
The patients trained at home on a stationary bike three times weekly for ten weeks. The patients were provided with stationary bikes and instructed in the set-up of the bike. It was not important that they trained on a specific type of stationary bike. They were instructed to have a small flexion of 5–15 degrees in their knee when they sat on the bike with the leg stretched. They were advised to cycle with the same cadence as used at the peak exercise test, between 60–80 RPM. The intensity was controlled by a pulse interval corresponding to 70% of their VO2max as determined from the peak exercise test. The duration of the training sessions increased from 20 minutes during the first two weeks to 30 minutes the last eight weeks. The training was always initiated by a 5-10-minute warm-up to allow the patients to reach their pulse interval gradually before starting the training session.
Compliance was monitored by downloading data from pulse watches. The patients also kept a diary of their training sessions and recorded adverse effects. Patients were phoned weekly to facilitate compliance.
Primary outcome measures
Primary efficacy was change in VO2max and fatigue (FSS questionnaire). VO2max is an indicator of cardiovascular fitness and aerobic endurance, and a change reflects the physiological response to training. Patients were not told prior to testing that training might improve their fatigue.
Ethics and statistics
The Regional Committee on Health Research Ethics of the Capital Region of Denmark approved the study (H-2-2013-066), and written informed consent was obtained from all patients.
Values are mean ± standard error, unless otherwise stated. Changes were assessed by a paired Student t-test, and a p-value < 0.05 (two tailed testing) was considered significant. Some results, when indicated, were assessed by a mixed Anova test.
Results
Demographic data of the patients
The included patients represent patients with CM, who have mutations in a broad range of genes (Table 1). The mean BMI for the patients was normal (Table 1). Two patients had a BMI of 13, which is not an uncommon finding in patients with CM [2].
Compliance and dropouts
Due to a high dropout rate, only seven of sixteen patients finished the training program (Fig 1A). Compliance was high in those who finished the training program. They completed 26–32 training sessions of 30 target sessions during the 10 weeks.
Nine patients dropped out of the training program, and fatigue was a major reason for dropping out for six of the patients. One patient dropped out due to personal matters, and two patients were lost to follow-up. None of the dropouts exercised for longer than half of the training period before exclusion and were therefore not evaluated for efficacy according to the protocol.
Peak oxidative capacity, workload and plasma CK levels
Training caused a significant increase in VO2max from 28 ± 3 to 31 ± 4 ml O2 · kg-1 · min-1 (range of increase, 1.9–7.1 ml O2 · kg-1 · min-1) (Fig 1B). Parallel changes were seen in peak workload (Fig 1C). Mean peak heart rate was 184 ± 4 before and 183 ± 2 after 10 weeks of training in the intervention group. No change was seen in the non-intervention group with an average VO2max of 31 ± 3 at baseline vs. 30 ± 3 ml O2 · kg-1 · min-1 at 10 weeks (Fig 1B).
All patients had stable CK levels during training (before, 92 ± 34; after, 80 ± 25 U/l; p = 0.334) (Fig 1D).
Functional tests, muscle strength, FVC and questionnaires
No changes were seen in any of the functional tests or SF36 questionnaire in either group (see Table 2). Baseline MRC scores are shown in Fig 2. FVC (n = 15) as percentage of predicted values were lower than seen in age-, sex- and height-matched healthy subjects (69 ± 5% of normal). Baseline FSS scores (n = 14) showed severe fatigue (5.1 ± 0.4), which is concordant to observations found in other CM patients [4]. FSS scores from the intervention group tended to decrease following training from 4.9 ± 1.9 to 4.4 ± 1.7 (p = 0.08).
A significant difference was found between the two groups in three muscle groups; ankle plantar flexion, * p < 0.001; ankle dorsal flexion, ** p = 0.032; hip abduction, *** p = 0.014. Error bars indicate standard error of the mean.
Discussion
This study indicates that 10 weeks of moderate-intensity, endurance training on a cycle ergometer is safe and an efficient way to improve fitness. But it is difficult to apply this therapy to all patients with CM due to fatigue. If trained, fatigue can potentially be reduced in patients with CM. Training improved VO2max significantly by 14% in the seven patients who completed the training program. No change was seen in mean peak heart rate indicating that the change was independent of will of the patient trying to push harder or encouragements by the un-blinded investigator. Improving fitness in patients with CM probably has other beneficial effects, as it is known that higher levels of physical fitness delay all-cause mortality, including lower rates of cardiovascular disease and cancer [13]. This is important, since patients with neuromuscular diseases are at higher risk of developing cardiovascular risk factors as a part of metabolic syndrome [5].
Although most patients carry mutations in genes encoding sarcomeric proteins or other contraction-excitation coupling related mechanisms, exercise does not appear to cause sarcomeric injury, since CK values were stable during the intervention and patients reported no myalgia. The improvement corresponds to improvements seen in similar training programs for patients with different types of muscular dystrophies [6–10].
Training of patients with other muscle diseases has shown unchanged or reduced fatigue following training. In our study, fatigue tended to decrease with training, which is of particular interest in this group, as fatigue is a disabling symptom in the every day life of patients with CM [4]. Fatigue was also the main single cause for dropping out. Nine patients dropped out of the training program, six of them due to fatigue. Fatigue therefore poses a limitation for initiating training in patients with CM, which is unlike the experience in other muscle diseases. However, fatigue is a major contributing factor for the lack of training effects in patients with motor neuron diseases [12, 14]. Unfortunately, fatigue was not assessed over time in the non-intervention group for comparison. However, fatigue is not likely to change in such a short period of time without interventions, as CMs are largely non-progressive. Pulmonary function tests showed a rather mild impairment, and only one patient used nocturnal respiratory assistance (Table 1). No correlation was seen between the FVC and FSS scores. It is therefore unlikely that increased fatigue in our patients with CM was caused by respiratory failure. Despite weekly phone contact between the investigator and the patient, patients were not compliant.
Since CM subtypes are very rare, it was necessary to include patients with different genetic backgrounds. Training responses could differ among CM genotypes and gender. However, training had the same consistent positive effect across all patients studied, which indicates that training is beneficial and safe in most types of CM.
The three functional tests were included, which improved with a similar training program in patients with LGMD2L (anoctamin 5 deficiency) [10]. However, no significant improvements were seen in patients with CM (see Table 2). This could relate to the short duration of the trial. Likely the improvements in endurance could translate into functional improvements if the training period had been prolonged, but future studies must investigate this.
Overall, the present study shows that for those CM patients who were able to complete the training, there was a significant improvement in VO2max, but it also illustrates how difficult it is to maintain CM patients on a training schedule, possibly due the high basal level of fatigue in this patient group. Alternative methods of training such as strength training or shorter training sessions at higher work intensities should be explored in CM.
Author Contributions
Conceived and designed the experiments: GH NW JV. Performed the experiments: GH CRV KH. Analyzed the data: GH NP JV. Contributed reagents/materials/analysis tools: GH NP JV. Wrote the paper: GH JV. Critical revision of manuscript: KH CRV NP NW JV.
References
- 1. Nance JR, Dowling JJ, Gibbs EM, Bönnemann CG. Congenital Myopathies: An Update. Curr Neurol Neurosci Rep 2012;12: 165–174. pmid:22392505
- 2. North KN, Wang CH, Clarke N, Jungbluth H, Vainzof M, Dowling JJ, et al. Approach to the diagnosis of congenital myopathies. Neuromuscul Disord 2014; 24: 97–116. pmid:24456932
- 3. Iannaccone ST, Castro D. Congenital Muscular Dystrophies and Congenital Myopathies. Contin Lifelong Learn Neurol 2013;19: 1509–1534.
- 4. Werlauff U, Højberg A, Firla-Holme R, Steffensen BF, Vissing J. Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale. Qual Life Res 2014;23: 1479–1488. pmid:24214178
- 5. Aitkens S, Kilmer DD, Wright NC, McCrory MA. Metabolic Syndrome in Neuromuscular Disease. Arch Phys Med Rehabil 2005;86: 1030–1036. pmid:15895353
- 6. Olsen DB, Orngreen MC, Vissing J. Aerobic training improves exercise performance in facioscapulohumeral muscular dystrophy. Neurol 2005;64: 1064–1066.
- 7. Ørngreen MC, Olsen DB, Vissing J. Aerobic training in patients with myotonic dystrophy type 1. Ann Neurol 2005;57: 754–757. pmid:15852373
- 8. Sveen ML, Jeppesen TD, Hauerslev S, Krag TO, Vissing J. Endurance training: An effective and safe treatment for patients with LGMD2I. Neurol 2007;68: 59–61.
- 9. Sveen ML, Jeppesen TD, Hauerslev S, Køber L, Krag TO, Vissing J. Endurance training improves fitness and strength in patients with Becker muscular dystrophy. Brain 2008;131: 2824–2831. pmid:18776212
- 10. Vissing CR, Preisler N, Husu E, Prahm KP, Vissing J. Aerobic training in patients with anoctamin 5 myopathy and hyperckemia. Muscle Nerve 2014;50: 119–123. pmid:24639367
- 11. Voet N, Bleijenberg G, Hendriks J, de Groot I, Padberg G, van Engelen B, et al. Both aerobic exercise and cognitive-behavioral therapy reduce chronic fatigue in FSHD: an RCT. Neurology 2014;83: 1914–1922. pmid:25339206
- 12. Madsen KL, Hansen RS, Preisler N, Thøgersen F, Berthelsen MP, Vissing J. Training improves oxidative capacity, but not function in Spinal Muscular Atrophy Type III. Muscle Nerve 2014;52: 240–244.
- 13. Blair SN, Kohl HW 3rd, Paffenbarger RS Jr, Clark DG, Cooper KH, Gibbons LW. Physical fitness and all-cause mortality: A prospective study of healthy men and women. JAMA 1989;262: 2395–2401. pmid:2795824
- 14. Preisler N, Andersen G, Thogersen F, Crone C, Jeppesen TD, Wibrand F, et al. Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease). Neurol 2009;72: 317–323.