Neuropediatrics 2004; 35(5): 262-266
DOI: 10.1055/s-2004-821173
Original Article

Georg Thieme Verlag KG Stuttgart · New York

Pilot Trial of Salbutamol in Central Core and Multi-Minicore Diseases

S. Messina[*] 1 , L. Hartley[*] 1 , M. Main2 , M. Kinali1 , H. Jungbluth1 , F. Muntoni1 , E. Mercuri1 , 3
  • 1Dubowitz Neuromuscular Centre, Department of Paediatrics, Imperial College, Hammersmith Hospital, London, UK
  • 2Department of Physiotherapy, Imperial College, Hammersmith Hospital, London, UK
  • 3Department of Paediatric Neurology, Catholic University, Rome, Italy
Further Information

Publication History

Received: February 5, 2004

Accepted after Revision: May 16, 2004

Publication Date:
10 August 2004 (online)

Abstract

Several studies have documented positive effects of β-adrenergic agonists on human skeletal muscle with regard to muscle mass and strength. The aim of this pilot study was to evaluate the effect of the β2-agonist salbutamol (albuterol) in a group of children with central core disease and multi-minicore disease. Thirteen patients, 8 with central core disease (mean age 17.5 years) and 5 with minicore disease (mean age 13.6 years) received oral salbutamol at a dose of 2 mg four times a day. Measures of efficacy were the change from baseline at 3 and 6 months in muscle strength, assessed by MRC score, myometry, functional measures and forced vital capacity. Statistical analysis was performed using repeated measures ANOVA (significance level < 0.05). Two patients with central core disease stopped the medication after one month because they did not notice any improvement and another one with minicore disease after 4 months because of increased tremors and palpitations. The remaining ten (6 with central core and 4 with minicore disease) completed the course of salbutamol without any significant adverse effects. There were significant increases in myometry, MRC scores and forced vital capacity between baseline and the six-month assessments. For both myometry and MRC the difference was already significant at 3 months and this was associated with a significant increase in functional abilities assessed with a structured functional scale. Our results suggest that salbutamol was overall well tolerated and might be beneficial in both central core and minicore patients. Larger prospective randomised, double-blind, placebo-controlled trials with salbutamol will be needed to confirm these preliminary findings.

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1 These authors contributed equally

Eugenio Mercuri

Department of Paediatrics
Hammersmith Hospital

Du Cane Road

London W12 OHN

UK

Email: e.mercuri@imperial.ac.uk

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