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

被引:47
作者
Becker, Matthijs L. [1 ,2 ]
Visser, Loes E. [1 ,2 ]
van Schaik, Ron H. N. [3 ,4 ]
Hofman, Albert [1 ,5 ]
Uitterlinden, Andre G. [1 ,5 ,6 ]
Stricker, Bruno H. Ch. [1 ,5 ,6 ,7 ]
机构
[1] Erasmus MC, Dept Epidemiol, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus MC, Hosp Pharm, NL-3000 CA Rotterdam, Netherlands
[3] Erasmus MC, Dept Clin Chem, NL-3000 CA Rotterdam, Netherlands
[4] STAR Med Diagnost Ctr, Rotterdam, Netherlands
[5] Netherlands Consortium Healthy Aging, Leiden, Netherlands
[6] Erasmus MC, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
[7] Inspectorate Hlth Care, Drug Safety Unit, The Hague, Netherlands
关键词
Organic Cation Transporter 1; Anti-Parkinson Agents; Pharmacogenetics; Pharmacoepidemiology; ORGANIC CATION TRANSPORTERS; DOPAMINE-D-2; AGONIST; PRAMIPEXOLE; KIDNEY; CELLS;
D O I
10.1007/s10048-010-0254-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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).
引用
收藏
页码:79 / 82
页数:4
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