Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b

Eur J Pediatr. 2009 Sep;168(9):1069-74. doi: 10.1007/s00431-008-0889-5. Epub 2008 Dec 9.

Abstract

Background: Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (GSD1b) phenotype. Recent studies indicated that activation of apoptosis and increased reactive oxygen species are implicated in the pathogenesis of neutropenia in GSD1b.

Methods: We studied seven GSD1b patients over a 2-year-period to evaluate the efficacy of vitamin E, a known antioxidant, in preventing or improving the clinical manifestations associated with neutropenia and neutrophil dysfunction. Frequency and severity of infections, neutrophil counts and function, ileocolonoscopy and intestinal histology, were monitored. During the first year, patients did not assume vitamin E; during the second year of the study, vitamin E supplementation was added to their therapeutic regimens.

Results: During vitamin E supplementation, the mean values of neutrophil counts were significantly higher (p < 0.05) and neutrophil counts lower than 500/mm(3) were found less frequently (p < 0.05); the frequency and severity of infections, mouth ulcers and perianal lesions, was reduced (p < 0.05); ileocolonoscopy and histology showed a mild improvement. Vitamin E supplementation did not result in changes in neutrophil function.

Conclusions: These results suggest that vitamin E supplementation might be beneficial in GSD1b patients and may alleviate disease manifestations associated with neutropenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antiporters / genetics
  • Bacterial Infections / epidemiology*
  • Bacterial Infections / prevention & control*
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Female
  • Glycogen Storage Disease Type I / drug therapy*
  • Glycogen Storage Disease Type I / genetics
  • Humans
  • Male
  • Monosaccharide Transport Proteins / genetics
  • Neutropenia / drug therapy*
  • Point Mutation / genetics
  • Prospective Studies
  • Treatment Outcome
  • Vitamin E / therapeutic use*
  • Young Adult

Substances

  • Antiporters
  • Monosaccharide Transport Proteins
  • SLC37A4 protein, human
  • Vitamin E