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

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 a...

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Autores principales: Becker, Matthijs L., Visser, Loes E., van Schaik, Ron H. N., Hofman, Albert, Uitterlinden, André G., Stricker, Bruno H. Ch.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029819/
https://www.ncbi.nlm.nih.gov/pubmed/20680652
http://dx.doi.org/10.1007/s10048-010-0254-5
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author Becker, Matthijs L.
Visser, Loes E.
van Schaik, Ron H. N.
Hofman, Albert
Uitterlinden, André G.
Stricker, Bruno H. Ch.
author_facet Becker, Matthijs L.
Visser, Loes E.
van Schaik, Ron H. N.
Hofman, Albert
Uitterlinden, André G.
Stricker, Bruno H. Ch.
author_sort Becker, Matthijs L.
collection PubMed
description 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).
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spelling pubmed-30298192011-03-16 OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users Becker, Matthijs L. Visser, Loes E. van Schaik, Ron H. N. Hofman, Albert Uitterlinden, André G. Stricker, Bruno H. Ch. Neurogenetics Short Communication 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). Springer-Verlag 2010-08-01 2011 /pmc/articles/PMC3029819/ /pubmed/20680652 http://dx.doi.org/10.1007/s10048-010-0254-5 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Short Communication
Becker, Matthijs L.
Visser, Loes E.
van Schaik, Ron H. N.
Hofman, Albert
Uitterlinden, André G.
Stricker, Bruno H. Ch.
OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title_full OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title_fullStr OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title_full_unstemmed OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title_short OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
title_sort oct1 polymorphism is associated with response and survival time in anti-parkinsonian drug users
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029819/
https://www.ncbi.nlm.nih.gov/pubmed/20680652
http://dx.doi.org/10.1007/s10048-010-0254-5
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