Skip to main content
Top
Published in: Journal of Neurology 6/2017

01-06-2017 | Original Communication

High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial

Authors: Grete Andersen, Karen Heje, Astrid Emile Buch, John Vissing

Published in: Journal of Neurology | Issue 6/2017

Login to get access

Abstract

Increasing evidence suggests that high-intensity training (HIT) is a time-efficient exercise strategy to improve fitness. HIT has never been explored in neuromuscular diseases, likely because it may seem counterintuitive. A single session of high-intensity exercise has been studied without signs of muscle damage in facioscapulohumeral muscular dystrophy type 1 (FSHD1). We aimed to determine whether HIT is safe and effective in FSHD1 in a randomized, controlled parallel study. Untrained adults with genetically verified FSHD1 (n = 13) able to perform cycle-ergometer exercise were randomized to 8 weeks of supervised HIT (n = 6) (3 × 10-min cycle-ergometer-HIT/week) or 8 weeks of usual care (n = 7). Following this, all participants performed 8 weeks of unsupervised HIT (3 × 10-min cycle-ergometer-HIT/week). Primary outcome was fitness, maximal oxygen uptake/min/kg body weight. Furthermore, workload, 6-min walk distance, 5-time sit-to-stand time, muscle strength, and daily activity levels were measured. Pain, fatigue, and plasma-CK were monitored. Twelve patients completed the randomized part of the study. Plasma-CK levels and pain scores were unaffected by HIT. Supervised HIT improved fitness (3.3 ml O2/min/kg, CI 1.2–5.5, P < 0.01, n = 6, NNT = 1.4). Unsupervised HIT also improved fitness (2.0 ml O2/min/kg, CI 0.1–3.9, P = 0.04, n = 4). There was no training effect on other outcomes. Patients preferred HIT over strength and moderate-intensity aerobic training. It may seem counterintuitive to perform HIT in muscular dystrophies, but this RCT shows that regular HIT is safe, efficacious, and well liked by moderately affected patients with FSHD1, which suggests that HIT is a feasible method for rehabilitating patients with FSHD1.
Literature
10.
go back to reference Andersen G, Ørngreen MC, Preisler N et al (2015) Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study. Am J Physiol Regul Integr Comp Physiol 308:R123–R130. doi:10.1152/ajpregu.00321.2014 CrossRefPubMed Andersen G, Ørngreen MC, Preisler N et al (2015) Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study. Am J Physiol Regul Integr Comp Physiol 308:R123–R130. doi:10.​1152/​ajpregu.​00321.​2014 CrossRefPubMed
12.
go back to reference van der Kooi EL, Vogels OJM, van Asseldonk RJGP et al (2004) Strength training and albuterol in facioscapulohumeral muscular dystrophy. Neurology 63:702–708CrossRefPubMed van der Kooi EL, Vogels OJM, van Asseldonk RJGP et al (2004) Strength training and albuterol in facioscapulohumeral muscular dystrophy. Neurology 63:702–708CrossRefPubMed
13.
go back to reference Gillen JB, Gibala MJ (2014) Is high-intensity interval training a time-efficient exercise strategy to improve health and fitness? Appl Physiol Nutr Metab Physiol Appliquée Nutr Métabolisme 39:409–412. doi:10.1139/apnm-2013-0187 CrossRef Gillen JB, Gibala MJ (2014) Is high-intensity interval training a time-efficient exercise strategy to improve health and fitness? Appl Physiol Nutr Metab Physiol Appliquée Nutr Métabolisme 39:409–412. doi:10.​1139/​apnm-2013-0187 CrossRef
14.
15.
16.
go back to reference Lamperti C, Fabbri G, Vercelli L et al (2010) A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. Muscle Nerve 42:213–217. doi:10.1002/mus.21671 CrossRefPubMed Lamperti C, Fabbri G, Vercelli L et al (2010) A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. Muscle Nerve 42:213–217. doi:10.​1002/​mus.​21671 CrossRefPubMed
19.
go back to reference Bankolé L-C, Millet GY, Temesi J et al (2016) Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy: a randomized controlled trial. Medicine (Baltimore) 95:e4497. doi:10.1097/MD.0000000000004497 CrossRef Bankolé L-C, Millet GY, Temesi J et al (2016) Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy: a randomized controlled trial. Medicine (Baltimore) 95:e4497. doi:10.​1097/​MD.​0000000000004497​ CrossRef
20.
go back to reference Eichinger K, Heatwole C, Heininger S et al (2016) Validity of the six minute walk test in facioscapulohumeral muscular dystrophy. Muscle Nerve. doi:10.1002/mus.25251 Eichinger K, Heatwole C, Heininger S et al (2016) Validity of the six minute walk test in facioscapulohumeral muscular dystrophy. Muscle Nerve. doi:10.​1002/​mus.​25251
21.
go back to reference Gliemann L, Gunnarsson TP, Hellsten Y, Bangsbo J (2015) 10-20-30 training increases performance and lowers blood pressure and VEGF in runners. Scand J Med Sci Sports 25:e479–e489. doi:10.1111/sms.12356 CrossRefPubMed Gliemann L, Gunnarsson TP, Hellsten Y, Bangsbo J (2015) 10-20-30 training increases performance and lowers blood pressure and VEGF in runners. Scand J Med Sci Sports 25:e479–e489. doi:10.​1111/​sms.​12356 CrossRefPubMed
Metadata
Title
High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial
Authors
Grete Andersen
Karen Heje
Astrid Emile Buch
John Vissing
Publication date
01-06-2017
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 6/2017
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-017-8497-9

Other articles of this Issue 6/2017

Journal of Neurology 6/2017 Go to the issue