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ABSTRACT: Background
Several lysosomal genes are associated with Parkinson's disease (PD), yet the association between PD and ARSA , which encodes for the enzyme arylsulfatase A, remains controversial.Objectives
To evaluate the association between rare ARSA variants and PD.Methods
To study possible association of rare variants (minor allele frequency<0.01) in ARSA with PD, we performed burden analyses in six independent cohorts with a total of 5,801 PD patients and 20,475 controls, using optimized sequence Kernel association test (SKAT-O), followed by a meta-analysis.Results
We found evidence for an association between functional ARSA variants and PD in four independent 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 UKBB cohort (P=0.005) and in the meta-analysis (P=0.049). However, despite replicating in four independent cohorts, these results should be interpreted with caution as no association survived correction for multiple comparisons. Additionally, we describe two families with potential co-segregation of the ARSA variant p.E384K and PD.Conclusions
Rare functional and loss-of-function ARSA variants may be associated with PD. Further replication in large case-control cohorts and in familial studies is required to confirm these associations.
SUBMITTER: Senkevich K
PROVIDER: S-EPMC10055435 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature
medRxiv : the preprint server for health sciences 20230313
<h4>Background</h4>Several lysosomal genes are associated with Parkinson's disease (PD), yet the association between PD and <i>ARSA</i> , which encodes for the enzyme arylsulfatase A, remains controversial.<h4>Objectives</h4>To evaluate the association between rare <i>ARSA</i> variants and PD.<h4>Methods</h4>To study possible association of rare variants (minor allele frequency<0.01) in <i>ARSA</i> with PD, we performed burden analyses in six independent cohorts with a total of 5,801 PD patients ...[more]