Back to Search
Start Over
Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced Dyskinesia.
- Source :
-
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2024 Oct; Vol. 39 (10), pp. 1773-1783. Date of Electronic Publication: 2024 Aug 12. - Publication Year :
- 2024
-
Abstract
- Background: Levodopa-induced dyskinesia (LID) is a common adverse effect of levodopa, one of the main therapeutics used to treat the motor symptoms of Parkinson's disease (PD). Previous evidence suggests a connection between LID and a disruption of the dopaminergic system as well as genes implicated in PD, including GBA1 and LRRK2.<br />Objectives: Our goal was to investigate the effects of genetic variants on risk and time to LID.<br />Methods: We performed a genome-wide association study (GWAS) and analyses focused on GBA1 and LRRK2 variants. We also calculated polygenic risk scores (PRS) including risk variants for PD and variants in genes involved in the dopaminergic transmission pathway. To test the influence of genetics on LID risk we used logistic regression, and to examine its impact on time to LID we performed Cox regression including 1612 PD patients with and 3175 without LID.<br />Results: We found that GBA1 variants were associated with LID risk (odds ratio [OR] = 1.65; 95% confidence interval [CI], 1.21-2.26; P = 0.0017) and LRRK2 variants with reduced time to LID onset (hazard ratio [HR] = 1.42; 95% CI, 1.09-1.84; P = 0.0098). The fourth quartile of the PD PRS was associated with increased LID risk (OR <subscript>fourth&#95;quartile</subscript> = 1.27; 95% CI, 1.03-1.56; P = 0.0210). The third and fourth dopamine pathway PRS quartiles were associated with a reduced time to development of LID (HR <subscript>third&#95;quartile</subscript> = 1.38; 95% CI, 1.07-1.79; P = 0.0128; HR <subscript>fourth&#95;quartile</subscript> = 1.38; 95% CI = 1.06-1.78; P = 0.0147).<br />Conclusions: This study suggests that variants implicated in PD and in the dopaminergic transmission pathway play a role in the risk/time to develop LID. Further studies will be necessary to examine how these findings can inform clinical care. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.<br /> (© 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.)
- Subjects :
- Humans
Male
Female
Aged
Middle Aged
Dopamine metabolism
Antiparkinson Agents adverse effects
Genetic Predisposition to Disease genetics
Polymorphism, Single Nucleotide genetics
Levodopa adverse effects
Parkinson Disease genetics
Parkinson Disease drug therapy
Dyskinesia, Drug-Induced genetics
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 genetics
Glucosylceramidase genetics
Genome-Wide Association Study
Subjects
Details
- Language :
- English
- ISSN :
- 1531-8257
- Volume :
- 39
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Movement disorders : official journal of the Movement Disorder Society
- Publication Type :
- Academic Journal
- Accession number :
- 39132902
- Full Text :
- https://doi.org/10.1002/mds.29960