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Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.

Publication ,  Journal Article
Biggar, WD; Politano, L; Harris, VA; Passamano, L; Vajsar, J; Alman, B; Palladino, A; Comi, LI; Nigro, G
Published in: Neuromuscul Disord
September 2004

We compare the long-term benefits and side effects of deflazacort using two treatment protocols from Naples (N) and Toronto (T). Boys with Duchenne muscular dystrophy between the ages of 8 and 15 years and who had four or more years of deflazacort treatment were reviewed. Diagnostic criteria included males with proximal muscle weakness evident before 5 years, increased serum creatine kinase and genetic testing and/or a muscle biopsy consistent with Duchenne muscular dystrophy. Thirty-seven boys were treated with protocol-N using deflazacort at a dose of 0.6 mg/kg per day for the first 20 days of the month and no deflazacort for the remainder of the month. Boys with osteoporosis received daily vitamin D and calcium. Deflazacort treatment started between 4 and 8 years of age. Thirty-two were treated with protocol-T using deflazacort at a dose of 0.9 mg/kg per day, plus daily vitamin D and calcium. Treatment started between 6 and 8 years of age. All boys were monitored every 4-6 months. The results were compared with age-matched controls in the two groups (19 for protocol-N and 30 for protocol-T). For the boys treated with protocol-N, 97% were ambulatory at 9 years (control, 22%), 35% at 12 years (control, 0%), 25% at 15 years (control, 0%). For the 32 boys treated with protocol-T, 100% were ambulatory at 9 years (control, 48%), 83% at 12 years (control, 0%) and 77% at 15 years (control, 0%). No aids or leg braces were used for ambulation. In boys 13 years and older, a scoliosis of >20 degrees developed in 30% of the boys on protocol-N, 16% on protocol-T and 90% of controls. For protocol-N, no cataracts were observed while in protocol-T, 30% of boys had asymptomatic cataracts that required no treatment. Fractures occurred in 19% (control 16%) of boys on protocol-N and 16% (control, 20%) of boys on protocol-T. This report illustrates: (a) the importance of collaborative studies in developing treatment protocols in Duchenne muscular dystrophy and (b) the long-term beneficial effects of deflazacort treatment in both protocols. However, the protocol-T seems to be more effective and frequently is associated with asymptomatic cataracts.

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Published In

Neuromuscul Disord

DOI

ISSN

0960-8966

Publication Date

September 2004

Volume

14

Issue

8-9

Start / End Page

476 / 482

Location

England

Related Subject Headings

  • Vitamin D
  • Treatment Outcome
  • Scoliosis
  • Psychomotor Performance
  • Pregnenediones
  • Neurology & Neurosurgery
  • Muscular Dystrophy, Duchenne
  • Motor Activity
  • Male
  • Immunosuppressive Agents
 

Citation

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Biggar, W. D., Politano, L., Harris, V. A., Passamano, L., Vajsar, J., Alman, B., … Nigro, G. (2004). Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols. Neuromuscul Disord, 14(8–9), 476–482. https://doi.org/10.1016/j.nmd.2004.05.001
Biggar, W. D., L. Politano, V. A. Harris, L. Passamano, J. Vajsar, B. Alman, A. Palladino, L. I. Comi, and G. Nigro. “Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.Neuromuscul Disord 14, no. 8–9 (September 2004): 476–82. https://doi.org/10.1016/j.nmd.2004.05.001.
Biggar WD, Politano L, Harris VA, Passamano L, Vajsar J, Alman B, et al. Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols. Neuromuscul Disord. 2004 Sep;14(8–9):476–82.
Biggar, W. D., et al. “Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.Neuromuscul Disord, vol. 14, no. 8–9, Sept. 2004, pp. 476–82. Pubmed, doi:10.1016/j.nmd.2004.05.001.
Biggar WD, Politano L, Harris VA, Passamano L, Vajsar J, Alman B, Palladino A, Comi LI, Nigro G. Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols. Neuromuscul Disord. 2004 Sep;14(8–9):476–482.
Journal cover image

Published In

Neuromuscul Disord

DOI

ISSN

0960-8966

Publication Date

September 2004

Volume

14

Issue

8-9

Start / End Page

476 / 482

Location

England

Related Subject Headings

  • Vitamin D
  • Treatment Outcome
  • Scoliosis
  • Psychomotor Performance
  • Pregnenediones
  • Neurology & Neurosurgery
  • Muscular Dystrophy, Duchenne
  • Motor Activity
  • Male
  • Immunosuppressive Agents