Abnormal glycogen in astrocytes is sufficient to cause adult polyglucosan body disease

Gene. 2013 Feb 25;515(2):376-9. doi: 10.1016/j.gene.2012.12.065. Epub 2012 Dec 21.

Abstract

Background: A 45-year old woman of Cambodian ethnic background presented with fatal respiratory failure due to a severe diaphragmatic dysfunction. Two years before, she had developed early onset of urinary symptoms.

Methods and results: Neuroimaging showed atrophy of the spine and medulla as well as a leukodystrophy affecting both supra- and infra-tentorial regions. At autopsy, polyglucosan bodies (PB) were seen in several peripheral tissues, including the diaphragm, and nervous tissues such as peripheral nerves, cerebral white matter, basal ganglia, hippocampus, brainstem and cerebellum. Immunohistochemistry and electron microscopy of the brain revealed an exclusive astrocytic localization of the PB. The diagnosis of adult polyglucosan body disease (APBD) was confirmed by enzymatic and molecular studies.

Conclusion: Storage of abnormal glycogen in astrocytes is sufficient to cause the leukodystrophy of APBD. Since brain glycogen is almost exclusively metabolized in astrocytes, this observation sheds light on the pathophysiology of APBD. In addition, this is the first report of an APBD patient presenting with a subacute diaphragmatic failure.

Publication types

  • Case Reports

MeSH terms

  • Astrocytes / metabolism*
  • Brain / pathology
  • DNA Mutational Analysis
  • Fatal Outcome
  • Female
  • Glucans / metabolism
  • Glycogen / metabolism
  • Glycogen Debranching Enzyme System / genetics
  • Glycogen Storage Disease / diagnosis*
  • Glycogen Storage Disease / genetics
  • Glycogen Storage Disease / pathology
  • Humans
  • Middle Aged
  • Mutation
  • Nervous System Diseases / diagnosis*
  • Nervous System Diseases / genetics
  • Nervous System Diseases / pathology

Substances

  • Glucans
  • Glycogen Debranching Enzyme System
  • Glycogen
  • polyglucosan
  • GBE1 protein, human

Supplementary concepts

  • Polyglucosan Body Disease, Adult Form