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Updated: Jul 25, 2025

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Association of Rare Variants in ARSA with Parkinson's Disease
Konstantin Senkevich1,2, Mariia Beletskaia3, Aliza Dworkind4
1The Neuro (Montreal Neurological Institute-Hospital), McGill University, Montreal, Quebec, Canada.
Background:
Several lysosomal genes are associated with Parkinson's disease (PD), yet the association between PD and ARSA remains unclear.
Objectives:
To study rare ARSA variants in PD.
Methods:
To study rare ARSA variants (minor allele frequency < 0.01) in PD, we performed burden analyses in six independent cohorts with 5801 PD patients and 20,475 controls, followed by a meta-analysis.
Results:
We found evidence for associations between functional ARSA variants and PD in four cohorts (P ≤ 0.05 in each) and in the meta-analysis (P = 0.042). We also found an association between loss-of-function variants and PD in the United Kingdom Biobank cohort (P = 0.005) and in the meta-analysis (P = 0.049). These results should be interpreted with caution as no association survived multiple comparisons correction. Additionally, we describe two families with potential co-segregation of ARSA p.E382K and PD.
Conclusions:
Rare functional and loss-of-function ARSA variants may be associated with PD. Further replications in large case-control/familial cohorts are required. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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