Brief Report
The DRD2 TaqIA polymorphism and demand of dopaminergic medication in Parkinson's disease
Article first published online: 3 JAN 2008
DOI: 10.1002/mds.21901
Copyright © 2007 Movement Disorder Society
Additional Information
How to Cite
Paus, S., Grünewald, A., Klein, C., Knapp, M., Zimprich, A., Janetzky, B., Möller, J. C., Klockgether, T. and Wüllner, U. (2008), The DRD2 TaqIA polymorphism and demand of dopaminergic medication in Parkinson's disease. Mov. Disord., 23: 599–602. doi: 10.1002/mds.21901
Publication History
- Issue published online: 26 MAR 2008
- Article first published online: 3 JAN 2008
- Manuscript Accepted: 18 NOV 2007
- Manuscript Revised: 16 NOV 2007
- Manuscript Received: 16 AUG 2007
Funded by
- Federal Ministry of Education and Research
- German Competence Network on Parkinson's disease, CNP. Grant Numbers: 01G19901, 01GI0201, 01GI0401
- NGFN. Grant Numbers: 01GS0115, NV-SO2T9
- BONFOR Program of the University of Bonn (UW)
- Volkswagen Foundation
- Abstract
- Article
- References
- Cited By
Keywords:
- Parkinson's disease;
- levodopa;
- DRD2;
- pharmacogenetics;
- German Competence Network on PD
Abstract
Previous studies have demonstrated that the TaqIA polymorphism of the D2 dopamine receptor gene (DRD2) is associated with response to dopaminergic and antidopaminergic treatment in Parkinson's disease (PD) and schizophrenia, respectively. We tested whether the TaqIA genotype in PD is responsible for demand of dopaminergic medication, measured in total dopaminergic load per year of disease, in a large scale association study based on the gene bank of the German Competence Network on Parkinson's disease. Regression analysis yielded no significant differences between the TaqIA genotypes. We conclude that the DRD2 TaqIA polymorphism alone has no pivotal role for interindividual variability of dopaminergic requirement in PD. We propose a practicable system of measuring dopaminergic treatment for future pharmacogenetic studies in PD. © 2007 Movement Disorder Society

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