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
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Aged, 80 and over
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Alleles
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Antiparkinson Agents / administration & dosage
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Antiparkinson Agents / pharmacokinetics
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Antiparkinson Agents / therapeutic use*
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Cohort Studies
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Female
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Humans
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Levodopa / administration & dosage
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Levodopa / pharmacokinetics
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Male
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Organic Cation Transporter 1 / genetics*
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Organic Cation Transporter 1 / metabolism
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Parkinson Disease / drug therapy*
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Parkinson Disease / genetics*
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Parkinson Disease / metabolism
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Parkinson Disease / mortality
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Pharmacogenetics
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Polymorphism, Single Nucleotide*
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Proportional Hazards Models
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Survival Analysis
Substances
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Antiparkinson Agents
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Organic Cation Transporter 1
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Levodopa