OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users

Neurogenetics. 2011 Feb;12(1):79-82. doi: 10.1007/s10048-010-0254-5. Epub 2010 Aug 1.

Abstract

Substrates for the Organic Cation Transporter 1, encoded by the SLC22A1 gene, are metformin, amantadine, pramipexole, and, possibly, levodopa. Recently, we identified that the rs622342 A > C polymorphism is associated with the HbA1c lowering effect in metformin users. In the Rotterdam Study, we associated this polymorphism with higher prescribed doses of all anti-Parkinsonian drugs. Between the first and fifth prescriptions for levodopa, for each minor rs622342 C allele, the prescribed doses were 0.34 defined daily dose higher (95% CI 0.064, 0.62; p=0.017). The mortality ratio after start of levodopa therapy was 1.47 times higher (95% CI 1.01, 2.13; p=0.045).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alleles
  • Antiparkinson Agents / administration & dosage
  • Antiparkinson Agents / pharmacokinetics
  • Antiparkinson Agents / therapeutic use*
  • Cohort Studies
  • Female
  • Humans
  • Levodopa / administration & dosage
  • Levodopa / pharmacokinetics
  • Male
  • Organic Cation Transporter 1 / genetics*
  • Organic Cation Transporter 1 / metabolism
  • Parkinson Disease / drug therapy*
  • Parkinson Disease / genetics*
  • Parkinson Disease / metabolism
  • Parkinson Disease / mortality
  • Pharmacogenetics
  • Polymorphism, Single Nucleotide*
  • Proportional Hazards Models
  • Survival Analysis

Substances

  • Antiparkinson Agents
  • Organic Cation Transporter 1
  • Levodopa