Brain biopterin and tyrosine hydroxylase in asymptomatic dopa-responsive dystonia

Ann Neurol. 2002 May;51(5):637-41. doi: 10.1002/ana.10175.

Abstract

It is assumed that brain biopterin and dopamine loss should not be as severe in asymptomatic dopa-responsive dystonia caused by GCH1 mutations as it is in symptomatic dopa-responsive dystonia. However, the actual status of dopaminergic systems in asymptomatic cases is unknown. In the autopsied putamen of an asymptomatic GCH1 mutation carrier, we found that brain biopterin loss (-82%) paralleled that reported in dopa-responsive dystonia patients (-84%). However, tyrosine hydroxylase protein and dopamine levels (-52 and -44%, respectively) were not as severely affected as in symptomatic patients (exceeding -97 and -88%, respectively). Our data suggest that the extent of striatal tyrosine hydroxylase protein loss may be critical in determining dopa-responsive dystonia symptomatology.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiparkinson Agents / therapeutic use
  • Biopterins / genetics*
  • Brain / enzymology
  • Brain / metabolism*
  • Brain / pathology
  • Dystonia / drug therapy*
  • Dystonia / enzymology*
  • Dystonia / genetics
  • Dystonia / metabolism
  • Fatal Outcome
  • Female
  • Humans
  • Levodopa / therapeutic use*
  • Middle Aged
  • Syndrome
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Antiparkinson Agents
  • Biopterins
  • Levodopa
  • Tyrosine 3-Monooxygenase