The role of apolipoprotein E polymorphisms in levodopa-induced dyskinesia

Acta Neurol Scand. 2011 Feb;123(2):117-21. doi: 10.1111/j.1600-0404.2010.01352.x.

Abstract

Objectives: To determine the relationship between apolipoprotein E (APOE) polymorphisms to the time to appearance of levodopa-induced dyskinesia (LID) in patients with Parkinson's disease.

Methods: The APOE genotype of 155 consecutive patients treated with levodopa was determined and its effect on the time of onset of LID was examined using Cox regression model, controlling for gender, age of disease onset, time to initiation of levodopa treatment and history of smoking.

Results: Two patients were homozygous for the APOE ε2 allele, 7 had ε2/ε3, 1 had ε2/ε4, 130 had ε3/ε3, 12 had ε3/ε4 and 3 had ε4/ε4; LID appeared in 57.4% of the patients, appearing 4.1 ± 3.5 years after the initiation of levodopa treatment. The survival curve for LID was not affected by the APOE genotype (P = 0.34).

Conclusion: APOE polymorphisms were found not to be associated with either the occurrence or the time to development of LID.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antiparkinson Agents / adverse effects*
  • Apolipoproteins E / genetics*
  • Dyskinesia, Drug-Induced / etiology*
  • Dyskinesia, Drug-Induced / genetics*
  • Dyskinesia, Drug-Induced / mortality
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Kaplan-Meier Estimate
  • Levodopa / adverse effects*
  • Male
  • Middle Aged
  • Parkinson Disease / drug therapy
  • Parkinson Disease / genetics
  • Polymorphism, Genetic / genetics*
  • Retrospective Studies

Substances

  • Antiparkinson Agents
  • Apolipoproteins E
  • Levodopa