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Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation

Abstract

Background

The European registry for individuals with GSD5 and other muscle glycogenosis (EUROMAC) was launched to register rare muscle glycogenosis in Europe, to facilitate recruitment for research trials and to learn about the phenotypes and disseminate knowledge about the diseases. A network of twenty collaborating partners from eight European countries and the US contributed data on rare muscle glycogenosis in the EUROMAC registry.

Methods

Following the initial report on demographics, neuromuscular features and comorbidity (2020), we here present the data on social participation, previous and current treatments (medication, supplements, diet and rehabilitation) and limitations. Furthermore, the following questionnaires were used: Fatigue severity scale (FSS), WHO Disability Assessment Scale (DAS 2.0), health related quality of life (SF36) and International Physical Activity Questionnaire (IPAQ).

Results

Of 282 participants with confirmed diagnoses of muscle glycogenosis, 269 had GSD5. Of them 196 (73%) completed all questionnaires; for the others, the data were incomplete. The majority, 180 (67%) were currently working. Previous medical treatments included pain medication (23%) and rehabilitation treatment (60%). The carbohydrate-rich diet was reported to be beneficial for 68%, the low sucrose diet for 76% and the ketogenic diet for 88%. Almost all participants (93%) reported difficulties climbing stairs. The median FSS score was 5.22, indicating severe fatigue. The data from the WHODAS and IPAQ was not of sufficient quality to be interpreted.

Conclusions

The EUROMAC registry have provided insight into the functional and social status of participants with GSD5: most participants are socially active despite limitations in physical and daily life activities. Regular physical activity and different dietary approaches may alleviate fatigue and pain.

Introduction

Glycogen storage disease type 5, GSD5 (McArdle disease) is a rare metabolic myopathy with a prevalence of approximately 1:100,000 [1]. It is caused by inherited deficiency of muscle glycogen phosphorylase, also known as myophosphorylase. GSD5 is characterized by physical activity intolerance manifesting as muscle fatigue, cramping and pain, during vigorous activities [1]. If continuing activity at the same intensity, individuals are at risk for rhabdomyolysis and myoglobinuria [2]. GSD5 is rare and has an autosomal recessive inheritance pattern and a variable presentation. As a consequence, many participants experienced a long diagnostic delay [4]. This is expected to improve with the wide availability of diagnostic next-generation sequencing [31]. Once diagnosed, symptomatic treatment is often not provided.

The European registry for individuals with GSD5 and other muscle glycogenosis (EUROMAC) was launched to raise awareness of diagnostic accuracy of muscle GSDs, improve care, and collect important clinical and epidemiological data for use in future clinical trials by Scalco et al. [3, 4] The first two EUROMAC reports focused on the design of the registry and the clinical and genetic characteristics and comorbidities. The main findings were a high frequency of fixed weakness, normal CK values in a minority of participants, body mass index above background population and a high prevalence of hypothyroidism and coronary heart disease. [3, 4] We here present the additional data collected in the EUROMAC registry, including scores on social participation, previous and current treatments, functional limitations, fatigue, health disability, quality of life and physical activity.

Methods

EUROMAC registry

The registry was designed under the guidance and consensus of EUROMAC members at specific meetings during the first months of the EUROMAC project. EUROMAC members were twenty collaborating partners from eight European countries (Denmark, France, Germany, Greece, Italy, Spain, Turkey and United Kingdom) and USA. The Netherlands and Poland joined the project later and contributed individuals to the registry. The registry obtained the approval of all local Institutional review Boards for patient entry via the registry website (www.registryeuromac.eu).

The technical setup and data security for the registry are detailed in [3]. After review by people affected by GSDs and by a patient representative to ensure clarity [5], the participant information sheet and consent form were translated into the languages of the participating countries and adapted to follow local regulations.

Participants and data entry

All participants consented in writing before inclusion in the registry. Any clinician working at a European institution was able to register on the EUROMAC platform and enter patient data after joining the EUROMAC partnership. Inclusion criteria were individuals with a diagnosis of one of the 14 known muscle GSDs either verified by genetic testing or enzymatic testing of the muscle biopsy. Individuals with Pompe disease were excluded as there was a well-established registry for this disease already. Following informed consent from the participant, data were pseudonymized and uploaded onto a safe, encrypted web-based registry. Recruited participants were able to log in, review their own information and complete selected sections with their personal experiences. None of the recruited participants or participating clinicians were allowed to see data from other participants.

Data entry items are shown in Table 3 by Pinos et al. [3] We here present the results collected in Sects. 6, 7 and 8 Data was only entered once, except if missing data was uploaded later. Data was based on clinical status and medical history at the time of data entry.

Customized questions

Participants were asked about Limitations (Sect. 6), Previous/ongoing treatments (Drugs, Special diet, Supplements, Rehabilitation program, Other treatments; Sect. 7), and Services provided (including current work involvement and adaptations; Sect. 8). Drugs were categorized in groups: Pain Relief, ACE Inhibitors, Diuretics, Cardiovascular Drugs, Insulin or Antidiabetics, Muscle Relaxants, Psychoactive Drugs, Allopurinol, and Other. In addition, participants were asked to provide details of the provided health care and rehabilitation and to report what was most beneficial.

Questionnaires

The following validated questionnaires were used: FSS (fatigue severity scale), WHODAS 2.0 (World Health Organization Disability Assessment Schedule), QoL/SF-36v2 (Quality of life/Short Form Health Survey) and IPAQ (International physical activity questionnaire). Data from the SF-36v2 was analyzed with Quality Metric Health Outcomes Scoring Software 5.0, data from the WHODAS 2.0 was converted to IRT (item-response-theory)-based scoring [6, 7] and data from the IPAQ was calculated to metabolic equivalent of task (MET)-min per week. [8,9,10]

We only used the data from the Dutch participants for the analyses of the SF-36v2 and IPAQ since the data of other countries were incomplete or not reliable. We refer to the results section for details of data.

Data analysis

Mainly descriptive statistics were used to analyze the data and performed by using IBM SPSS Statistics 25. Absolute numbers and percentages of the number of answers on the item are presented. Correlations between age and disease severity were calculated (Pearson correlation coefficient). Analyses for the open-question sections were performed by narrative analysis using ATLAS.ti 2.0. Axial coding was used for the analyses to identify relations between the data and categorized when referring to the same phenomenon.

Results

Participants

In total 282 participants with confirmed diagnoses of muscle glycogenosis were included between 2015 and 2018. 269 (95%) of them had GSD5.

This report only presents the data of the participants with GSD5. Of the 269 GSD5 participants, 196 (73%) completed all mandatory questionnaires; for other participants, data were incomplete. Table 1 in Scalco et al. shows the completeness of data entry for different items [4]. The number of participants that have provided an answer to a question are provided in the tables and figures. Figure 1 in the first EUROMAC report by Scalco et al. [4] provides an overview of the geographical origin of the participants. The majority (215; 80%) were from the UK (United Kingdom), Spain, Italy or the Netherlands.

Table 1 Descriptive statistics on previous treatments
Fig. 1
figure 1

Work Involvement. ‘Total’ shows the number of answers for the question. Currently Working demonstrates how many people are currently working. Job Change demonstrates how many people have changed their job due to their disease (GSD5). Job Modification demonstrates for how many people their employer modified their work environment because of their disease conditions (GSD5). Job Activity demonstrates what people are doing most of their time during work

Work participation

Figure 1 provides an overview of the participants’ work involvement. Seventy (67%) participants reported to be working at the time of the study (0–20 years: 40% working; 20–60 years: 67% working and > 60 years: 32% working); the other 35 (33%) stated that they were not currently working. Participants were not asked if they had been working in the past. 28 (29%) of the respondents stated that they changed their job due to GSD5 and 18 (22%) needed their employer to modify their work environment because of their disease. Thirty-six (51%) participants reported that they were most of their time sitting during work, while 25 (36%) were mostly walking and 9 (13%) reported to have strenuous physical activities during work.

Previous and ongoing treatments

Table 1 outlines which treatments the respondents had previously received of. Mostly used were medications for pain medication (n = 45; 23%), psychoactive drugs (n = 34; 18%), and cardiovascular drugs (n = 33; 17%). The types of pain medication that were used in this cohort are illustrated in Fig. 2. Paracetamol was used by 21 (47%) participants with or without other analgesic drugs, non-steroidal anti-inflammatory drugs (NSAID’s) by 10 (22%), and opioids by 8 (18%) of the participants. All 45 individuals who used pain-relief, indicated that they had done so to treat their GSD5 symptoms at some point in their lives.

Fig. 2
figure 2

This Pie Chart demonstrates the types of pain medication that is being used by the participants as previous treatment for GSD5. It also shows the percentages per type of pain medication. Total number of answers: 45

Fifty-five participants (32%) had been on a low sucrose diet, and 41 (76%) of them found this diet beneficial for their GSD5-related symptoms. Twenty-nine (17%) had been on a carbohydrate-rich diet, and 19 (68%) of them reported a beneficial effect. A minority of the participants reported a positive effect of a protein-rich and lipid-rich diet. Other dietary interventions (n = 13) are illustrated in Fig. 3, including the ketogenic diet and other healthy diets. Of this group, 15 (88%) reported that those diets had positive/beneficial effect.

Fig. 3
figure 3

This pie chart demonstrates the mentioned ‘Other’ Diets in the open-question that have been used as a previous treatment. Ketogenic diet, modified Atkins and carbohydrate free are very similar, together 35%. Total number of answers: 17

Supplements had not been used by many participants. Only three participants had used branched chain amino acids (BCAA), two of whom reported it to be beneficial. Other supplements that had been used as a previous treatment by this cohort are illustrated in Fig. 4: galactose (n = 5; 26%), multivitamins (n = 3; 16%) and vitamin D (n = 3; 16%); 5 (26%) participants of this group reported a positive/beneficial effect.

Fig. 4
figure 4

This pie chart demonstrates the mentioned ‘other’ supplements in the open-question that have been used as a previous treatment. Total number of answers: 19 *MCT: Medium-Chain-Triglyceride

Health care and rehabilitation

Table 2 provides a summary of the types of rehabilitation program that were reported as previous ongoing treatments. The most frequently reported form of rehabilitation was walking (n = 69 (60%)). Physical therapy, muscle massage, working out in a gym and swimming also have been used more frequently than other programs.

Table 2 Program type of rehabilitation

Table 3 provides an overview of provided health care and rehabilitation. Physical therapy was reported to be mostly beneficial in the open questions (n = 10; 23%). Other beneficial approaches included receiving support for disabled workers, available literature and advice and the clinical assessments and follow-ups. Those types of health care have helped the participants with GSD5 related struggles.

Table 3 Health care details

The limitations the participants with GSD5 reported to experience in their everyday life are presented in Table 4. Almost all (n = 79; 93%) experienced limitations in climbing stairs. Also, limitations in running (n = 76; 89%), walking fast (n = 72; 85%) and carrying shopping bags (n = 69; 81%) were frequently reported.

Table 4 Limitations

Validated questionnaires

The results of the QoL, FSS, IPAQ and WHODAS are included in Table 5. We excluded data of the QoL, IPAQ and WHODAS from unrealistic (outside the range, below or above the standardized limit) and/or incomplete scores, resulting in the inclusion between 21 and 34 responses. For the analyses of the QoL we only used data from the Dutch sub cohort, since this data set was complete and accurate. Other sub-cohorts did not include any realistic or complete scores.

Table 5 Descriptive statistics on validated questionnaires

Fatigue. The median for the FSS was 5.22 [1.7;7]. Twenty-nine out of 34 participants had a FSS score of ≥ 4. Since a score of ≥ 4 generally indicates severe fatigue [11], this sample is considered to be severely fatigued.

Quality of life

The median for the total score of the SF-36 is 60 [16.0;80.0]. Higher scores indicate a higher quality of life. Compared to healthy adolescents the scores of the QoL for GSD5 participants were well below the normal range, especially the score of the physical functioning (PF) which was the lowest of all measures (44,8).

Disability. The median IRT-based range score for the WHODAS 2.0, is 10 [1.0;43.0]. The higher the domain score, the higher the level of experienced disability. The correlation between age and disability (measured by WHODAS) was analyzed, and due to the significance level being above the threshold (p < 0.05), this correlation is not considered statistically significant.

Physical activity

The median score on the IPAQ was 2491 [0.0;38,681.0]. MET-min/week and 20 out of 26 participants scored a low physical activity. With the calculated MET-min per week we can conclude that this sample scored a low physical activity since the score did not exceed the minimum criteria of 3000 METs. [9, 10]

Discussion

The EUROMAC registry was created to ensure data collection and its maintenance with the aim to improve diagnosis and care for individuals with rare glycogen storage diseases. The registry increases knowledge from clinical data from individuals with GSD5 and related conditions and has played a positive role in promoting translational research [3]. Moreover, it is one of few international registry of muscle glycogenosis available. Besides unraveling phenotypic characteristics of GSD5 as seen in the accompanying papers [3, 4], the current report provides insight in the previous treatments, functional limitations, fatigue, health disability, quality of life and physical activity. We will discuss the main findings below.

The number of participants currently working (67%) is in line with the proportion of the general adult population that is working in various European countries: 72% in the Netherlands [13], 76% in the UK [25], and 66% in Spain [26]. This normal labor force participation rate might be related to the reported adaptations: 29% had changed their job and 22% had their work environment modified. Reported physical activity during work is variable, including sitting and non-sitting labor.

In line with previous studies, many participants reported use of medication to relieve pain. Both over the counter and prescribed drugs were used, mostly paracetamol (acetaminophen). Paracetamol is unlikely to relieve acute muscle pain but may be taken to manage more severe pain, which may last for hours after exercise [14]. Furthermore, 26% of participants reported opioid medication in combination with other analgesic drugs. This is not recommended, as these drugs may mask feedback from muscles, leading to further muscle damage and recurring pain [14]. The recently published Clinical Practice Guidelines recommend a regular exercise program as a safe manner to reduce chronic pain [14,15,16,17]. Other drugs commonly used are psychoactive drugs (18% compared to 5.5% in general population) and cardiovascular drugs (17% compared to), which make sense since a high rate of coronary heart disease was described in the EUROMAC paper [4]. For comparison, 10.7% of U.S. adults used one or more prescribed pain medications in the past 30 days; 13% of males use over the counter analgesics weekly and 11.9% of US adults reported having used opioids in the past 12 months (data mainly from USA, 2015–2018) [32,33,34].

Most of the participants who used a sucrose supplementation and carbohydrate rich diet found it beneficial. The beneficial effects of oral sucrose supplementation before exercise are well established [14, 19, 29]. Also, a carbohydrate rich diet has shown to attenuate muscle pain in the first few minutes of exercise before the second wind compared to a protein rich diet and has proven beneficial because it maintains the hepatic glycogen stores [14, 20, 21]. Both the protein-rich and the lipid-rich diet were reported as not beneficial for our cohort but only by a low sample size. Still, improvement in parameters for the sucrose supplementation and carbohydrate rich diet need to be studied since none indicated significant clinical benefits.

In the open-questions the ketogenic diet was reported as beneficial. Other studies that have investigated the effects of a modified ketogenic diet in individuals with GSD5 and one informal survey showed improvement in symptoms and exercise tolerance for most of the cohort after using the ketogenic diet. [22, 23] The BCAA supplementation was found beneficial for 67% but since only 3 participants have used it, not much can be concluded.

The reported rehabilitation programs are in line with recommended physical and occupational therapy. Remarkably, 60% of the participants reported walking as an important rehabilitation approach. The international patient support group IamGSD has promoted walking as a training for GSD5 for years [24]. Also, walking can easily be implemented in daily life. Future research could focus on objectively demonstrating the positive effect of walking and other forms of aerobic exercise in daily life. The inclusion of participants in the registry may have resulted in a higher proportion of individuals who are more active, presumably both mentally and physically, as they actively seek medical assistance. However, caution should be exercised due to the potential overestimation of rehabilitation use stemming from selection bias.

Moreover, for comparison of fatigue, the FSS score for individuals with Lyme disease is 4.8, Parkinson’s disease is 4.1 and for a healthy population it is 2.3. [11, 12, 30]

Limitations of this study include the collection of retrospective data and the issue of missing data, which reduces the validity. The data was collected in the prospective EUROMAC registry and had to be entered by various researchers and clinicians. This carries the risk of observation or confirmation bias in case of subjective outcome measures. The data from the WHODAS was not of sufficient quality to be interpreted further. It is also important to note that the present study had a limited number of correlation analyses, which may restrict the generalizability of the findings and the ability to explore potential relationships between additional variables of interest. Furthermore, to have researchers and clinicians enter the patient-reported outcome measures scores was challenging. It has led to missing data and implies propensity to error. Prospective patient registries where patient-reported outcome measures (PROMS) are completed by patients themselves are expected to have a better validity [27, 28]. Nevertheless, the EUROMAC has raised awareness of diagnostic accuracy and collected important data for use in future clinical trials with the accompanying papers [3, 4].

Conclusions

The EUROMAC registry helps to gain more understanding of GSD5. It provides inspiration for other clinicians to develop patient registries for other rare diseases. The analyses in this paper has given insight into the functional limitations and treatments and rehabilitation approaches used. The findings support the recent international recommendations for people with GSD5, including adopting an active, healthy lifestyle and careful use of analgesic drugs. Moreover, participants that used diet and supplementation mentioned beneficial effects. This can be promising, however placebo-controlled studies with larger cohorts are warranted to provide conclusive evidence of the effects of these diets and supplementations.

Availability of data and materials

Only data that is relevant and not analyzed before is included in this article. Other data are reported in the accompanied paper by Scalco et al. in 2020 in this journal [4]. The database is available upon reasonable request to the EUROMAC consortium.

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Acknowledgements

EUROMAC was supported by several patients’ associations and large networks of patient registries, such as the Association for Glycogen Storage Disease (https://agsd.org.uk/) and the EPIRARE Group on Rare Disease Registries (https://www.eurordis.org/content/epirare). The European Neuromuscular Centre (https://www.enmc.org/) also supported the project by contributing to the organization and funding of a dedicated workshop. We are grateful to all the participants for their participation in EUROMAC.

Funding

W. Karazi received financial support of Stichting McArdle and Stichting Stofwisselkracht, two non-profit foundations in the Netherlands that support research on McArdle disease and metabolic disorders in general.

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Contributions

WK contributed to data analysis, data interpretation, and writing of the manuscript. RSS contributed to the design of the study, data collection, data analysis, and data interpretation. MGS contributed to the design of the study, data collection, data analysis, and data interpretation. NL to the data collection, data analysis, and data interpretation. AL contributed to the design of the study, data collection, data analysis, and data interpretation. AS contributed to the design of the study, data collection, data analysis, and data interpretation. AM contributed to the design of the study, data collection, data analysis, and data interpretation. MV contributed to the design of the study, data collection, data analysis, and data interpretation. GR contributed to the design of the study, data collection, data analysis, and data interpretation. AT contributed to the design of the study, data collection, data analysis, and data interpretation. OM contributed to the design of the study, data collection, data analysis, and data interpretation. CVK contributed to the data collection, data analysis, and data interpretation. PL contributed to the design of the study, data collection, data analysis, and data interpretation. BSM contributed to the design of the study, data collection, data analysis, and data interpretation. IV contributed the design of the study, data collection, data analysis, and data interpretation. GS contributed to the design of the study, data collection, data analysis, and data interpretation. EK contributed to the design of the study, data collection, data analysis, and data interpretation. RT contributed to the design of the study, data collection, data analysis, and data interpretation. SS contributed to the design of the study, data collection, data analysis, and data interpretation. HD contributed to the design of the study, data collection, data analysis, and data interpretation. BK contributed to the design of the study, data collection, data analysis, and data interpretation. AW contributed to the design of the study, data analysis, and data interpretation. ALA contributed to the design of the study, data collection, data analysis, and data interpretation. TP contributed the design of the study, data collection, data analysis, data interpretation, and the writing of the manuscript. RM contributed to the design of the study, data collection, data analysis, and data interpretation.. RQ contributed to the design of the study, data collection, data analysis, and data interpretation. JV contributed to the design of the study, data collection, data analysis, data interpretation, and the writing of the manuscript. NCV contributed to the design of the study, data collection, data analysis, data interpretation, and the writing of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Nicol C. Voermans.

Ethics declarations

Ethics approval and consent to participate

The registry was designed under the guidance and consensus of EUROMAC members at specific meetings during the first months of the EUROMAC project. EUROMAC members were twenty collaborating partners from eight European countries (Denmark, France, Germany, Greece, Italy, Spain, Turkey and United Kingdom) and USA. The Netherlands and Poland joined the project later and contributed individuals to the registry. The registry obtained the approval of all local Institutional review Boards for patient entry via the registry website (www.registryeuromac.eu). The technical setup and data security for the registry are detailed in [3]. After review by people affected by GSDs and by a patient representative to ensure clarity [5], the participant information sheet and consent form were translated into the languages of the participating countries and adapted to follow local regulations.

Consent for publication

All participants gave informed consent for analysis and publication of the data obtained from this study.

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There are no competing interests.

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Karazi, W., Scalco, R.S., Stemmerik, M.G. et al. Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation. Orphanet J Rare Dis 18, 210 (2023). https://doi.org/10.1186/s13023-023-02825-z

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