4.6 Article

Motor Progression of Parkinson's Disease with the Leucine-Rich Repeat Kinase 2 G2019S Mutation

Journal

MOVEMENT DISORDERS
Volume 29, Issue 8, Pages 1057-1060

Publisher

WILEY-BLACKWELL
DOI: 10.1002/mds.25931

Keywords

LRRK2; genetic; disease progression; Parkinson's disease

Funding

  1. Bharier Medical Fund

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Introduction: In this retrospective study, we compared motor disease progression in Ashkenazi-Jewish (AJ) Parkinson's disease (PD) patients carrying the LRRK2*G2019S mutation with that of noncarriers. Methods: Consecutive PD patients were recruited between 2004 and 2011. Disease progression of carriers versus noncarriers was compared using survival analysis, where the end-point was the time from PD onset to reaching Hoehn and Yahr stage 3 (HY3). Results: Overall, 405 AJ PD patients (males = 241[60%]) were genotyped, of whom 60 (males = 30) were LRRK2*G2019S mutation carriers. Time to HY3 did not differ significantly between mutation carriers and noncarriers (hazard ratio = 1.21, 95% CI = 0.83-1.77, P = 0.33). Age at PD onset was younger for carriers than for noncarriers (59.1 +/- 9.8 vs. 63.2 +/- 12.0 years, respectively; P = 0.005). In both groups, young age at onset was strongly associated with longer time to HY3, (P < 0.001). Conclusion: The LRRK2*G2019S mutation status has no discernible effect on the rate of motor disease progression in AJ PD patients. (C) 2014 International Parkinson and Movement Disorder Society

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