Catechol-O-methyltransferase Val158Met and the Risk of Dyskinesias in Parkinson's Disease

Lonneke M. L. de Lau, Dagmar Verbaan, Johan Marinus, Peter Heutink, Jacobus J. van Hilten

Research output: Contribution to journalArticleAcademicpeer-review

67 Citations (Scopus)

Abstract

Background: The A-allele of the catechol-O-methyltransferase (COMT) Val158Met polymorphism is associated with decreased enzymatic activity and higher dopamine availability. Methods: We studied 219 patients with PD who were free of dyskinesias at baseline and underwent thorough annual examinations. Results: The A-allele of the COMT Val158Met polymorphism was related to an increased risk of developing dyskinesias during follow-up, in a dose-dependent manner (adjusted hazard ratios for the AG and AA genotypes [compared to GG]: 2.09 [95% confidence interval (CI), 1.07-4.06] and 2.81 [CI, 1.43-5.54], respectively). Conclusions: This finding suggests that genetic factors may affect susceptibility to dyskinesias in PD. (C) 2011 Movement Disorder Society
Original languageEnglish
Pages (from-to)132-135
JournalMovement disorders
Volume27
Issue number1
DOIs
Publication statusPublished - 2012

Cite this