Classification of GBA1 Variants in Parkinson's Disease: The GBA1‐PD Browser

Author:

Parlar Sitki Cem12,Grenn Francis P.3,Kim Jonggeol Jeffrey34,Baluwendraat Cornelis35ORCID,Gan‐Or Ziv126ORCID

Affiliation:

1. Department of Human Genetics McGill University Montréal Québec Canada

2. The Neuro (Montreal Neurological Institute‐Hospital), McGill University Montréal Québec Canada

3. Laboratory of Neurogenetics National Institute on Aging Bethesda Maryland USA

4. Preventive Neurology Unit, Centre for Prevention Diagnosis and Detection Wolfson Institute of Population Health, Queen Mary University of London London United Kingdom

5. Center for Alzheimer's and Related Dementias National Institutes of Health Bethesda Maryland USA

6. Department of Neurology and Neurosurgery McGill University Montréal Québec Canada

Abstract

AbstractBackground GBA1 variants are among the most common genetic risk factors for Parkinson's disease (PD). GBA1 variants can be classified into three categories based on their role in Gaucher's disease (GD) or PD: severe, mild, and risk variant (for PD).ObjectiveThis review aims to generate and share a comprehensive database for GBA1 variants reported in PD to support future research and clinical trials.MethodsWe performed a literature search for all GBA1 variants that have been reported in PD. The data have been standardized and complemented with variant classification, odds ratio if available, and other data.ResultsWe found 371 GBA1 variants reported in PD: 22 mild, 84 severe, 3 risk variants, and 262 of unknown status. We created a browser containing up‐to‐date information on these variants (https://pdgenetics.shinyapps.io/GBA1Browser/).ConclusionsThe classification and browser presented in this work should inform and support basic, translational, and clinical research on GBA1‐PD. © 2023 International Parkinson and Movement Disorder Society.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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