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A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome.

Publication ,  Journal Article
Trojan, DA; Collet, JP; Shapiro, S; Jubelt, B; Miller, RG; Agre, JC; Munsat, TL; Hollander, D; Tandan, R; Granger, C; Robinson, A; Finch, L ...
Published in: Neurology
October 12, 1999

BACKGROUND: Postpoliomyelitis syndrome (PPS) is likely due to degeneration and dysfunction of terminal axons of enlarged postpolio motor units. Age-related decline in growth hormone and insulin-like growth factor (IGF-I) may be a contributing factor. Neuromuscular junction abnormalities and decreased IGF-I levels may respond to the anticholinesterase pyridostigmine, with consequent improvement in strength, fatigue, and quality of life. OBJECTIVES: To determine the effect of pyridostigmine in PPS on health-related quality of life, isometric muscle strength, fatigue, and serum IGF-I levels; and to assess the safety of pyridostigmine in PPS. METHODS: The study was a multicenter, randomized, double-blinded, placebo-controlled trial of a 6-month course of pyridostigmine 60 mg three times per day in 126 PPS patients. The primary data analysis compared mean changes of outcomes between treatment and control groups at 6 months using an intention to treat approach. Secondary analyses included a comparison of outcomes at 6 and 10 weeks, and in compliant patients. RESULTS: The study showed no significant differences in pyridostigmine and placebo-treated patients with regard to changes in quality of life, isometric strength, fatigue, and IGF-I serum levels at 6 months in the primary analysis and in compliant patients. There were no differences in outcomes at 6 and 10 weeks between groups. However, very weak muscles (1 to 25% predicted normal at baseline) were somewhat stronger (p = 0.10, 95% CI of difference -9.5 to 73.3%), and in compliant patients IGF-I was somewhat increased (p = 0.15, 95% CI of difference -6.4 to 44.8 ng/mL) at 6 months with the medication. Pyridostigmine was generally well tolerated. CONCLUSIONS: This study showed no significant differences between pyridostigmine and placebo-treated PPS patients on measures of quality of life, isometric strength, fatigue, and serum IGF-I.

Duke Scholars

Published In

Neurology

DOI

ISSN

0028-3878

Publication Date

October 12, 1999

Volume

53

Issue

6

Start / End Page

1225 / 1233

Location

United States

Related Subject Headings

  • Pyridostigmine Bromide
  • Postpoliomyelitis Syndrome
  • Neurology & Neurosurgery
  • Middle Aged
  • Male
  • Humans
  • Female
  • Double-Blind Method
  • Aged
  • 3209 Neurosciences
 

Citation

APA
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Trojan, D. A., Collet, J. P., Shapiro, S., Jubelt, B., Miller, R. G., Agre, J. C., … Cashman, N. R. (1999). A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome. Neurology, 53(6), 1225–1233. https://doi.org/10.1212/wnl.53.6.1225
Trojan, D. A., J. P. Collet, S. Shapiro, B. Jubelt, R. G. Miller, J. C. Agre, T. L. Munsat, et al. “A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome.Neurology 53, no. 6 (October 12, 1999): 1225–33. https://doi.org/10.1212/wnl.53.6.1225.
Trojan DA, Collet JP, Shapiro S, Jubelt B, Miller RG, Agre JC, et al. A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome. Neurology. 1999 Oct 12;53(6):1225–33.
Trojan, D. A., et al. “A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome.Neurology, vol. 53, no. 6, Oct. 1999, pp. 1225–33. Pubmed, doi:10.1212/wnl.53.6.1225.
Trojan DA, Collet JP, Shapiro S, Jubelt B, Miller RG, Agre JC, Munsat TL, Hollander D, Tandan R, Granger C, Robinson A, Finch L, Ducruet T, Cashman NR. A multicenter, randomized, double-blinded trial of pyridostigmine in postpolio syndrome. Neurology. 1999 Oct 12;53(6):1225–1233.

Published In

Neurology

DOI

ISSN

0028-3878

Publication Date

October 12, 1999

Volume

53

Issue

6

Start / End Page

1225 / 1233

Location

United States

Related Subject Headings

  • Pyridostigmine Bromide
  • Postpoliomyelitis Syndrome
  • Neurology & Neurosurgery
  • Middle Aged
  • Male
  • Humans
  • Female
  • Double-Blind Method
  • Aged
  • 3209 Neurosciences