Successful use of albuterol in a patient with central core disease and mitochondrial dysfunction.

L. T. Schreuder, M. W. Nijhuis-van der Sanden, A. de Hair, G. Peters, S. Wortmann, L. A. Bok, E. Morava

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13 Scopus citations


Albuterol, a selective beta-adrenergic agonist, has been used experimentally in combination with exercise therapy in a few inherited neuromuscular disorders to increase muscle strength and muscle volume . We report on a 9-year-old boy with central core disease and mitochondrial dysfunction due to compound heterozygous RYR1 mutations receiving albuterol treatment for 1 year. Throughout the period of albuterol administration, the patient underwent an aerobic exercise regime of training sessions three times a week that lasted 20 min each. No side effects of albuterol use were seen. Significant clinical progress, including self care, sitting up, raising arms above the shoulders, independent feeding, and better speech and writing were observed compared with minimal development of these abilities in the previous years on physiotherapy. Improved forced expiratory volume in 1 s (FEV1) score was detected and increased muscle strength was noted: progress was measured using various functional tests and assessment scales. The only complication observed was a mild progression of the joint contractures, possibly due to an unbalance between the flexor and extensor musculature. In general, in this pilot study in a complex case of metabolic myopathy our patient has shown promising results following albuterol treatment and aerobic exercise therapy.

Original languageEnglish (US)
Pages (from-to)S205-209
JournalJournal of inherited metabolic disease
Volume33 Suppl 3
StatePublished - Dec 2010

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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