DRD2 haplotype is associated with dyskinesia induced by levodopa therapy in Parkinson's disease patients

Pharmacogenomics. 2012 Nov;13(15):1701-10. doi: 10.2217/pgs.12.149.

Abstract

Aim: Dyskinesia and motor fluctuation are frequent and serious complications of chronic levodopa therapy in patients with Parkinson's disease. Since genetic factors could play a role in determining the occurrence of these problems, the aim of the present study was to investigate whether possible functional polymorphisms among DRD2 and ANKK1 genes are associated with the risk of developing dyskinesia and motor fluctuations in Parkinson's disease patients.

Patients & methods: One hundred and ninety nine patients in treatment with levodopa were genotyped for the -141CIns/Del, rs2283265, rs1076560, C957T, TaqIA and rs2734849 polymorphisms at the DRD2/ANKK1 gene region.

Results: Carriers of the TTCTA haplotype showed an increased risk for the presence of dyskinesia (p = 0.007; 1.538 [95% CI: 1.126-2.101]).

Conclusion: Our data suggest an influence of the DRD2/ANKK1 gene region on levodopa-induced dyskinesia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Dyskinesia, Drug-Induced / enzymology
  • Dyskinesia, Drug-Induced / etiology*
  • Dyskinesia, Drug-Induced / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Levodopa / adverse effects*
  • Levodopa / therapeutic use*
  • Male
  • Middle Aged
  • Parkinson Disease / drug therapy*
  • Parkinson Disease / genetics*
  • Polymorphism, Genetic
  • Protein Serine-Threonine Kinases / genetics
  • Receptors, Dopamine D2 / genetics*

Substances

  • DRD2 protein, human
  • Receptors, Dopamine D2
  • Levodopa
  • ANKK1 protein, human
  • Protein Serine-Threonine Kinases