Towards a Global View of Parkinson's Disease Genetics

Author:

Khani Marzieh1ORCID,Cerquera‐Cleves Catalina23,Kekenadze Mariam45,Wild Crea Peter1,Singleton Andrew B.1,Bandres‐Ciga Sara1

Affiliation:

1. Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health Bethesda Maryland USA

2. Pontificia Universidad Javeriana, San Ignacio Hospital, Neurology Unit Bogotá Colombia

3. CHU de Québec Research Center, Axe Neurosciences, Laval University Quebec City Quebec Canada

4. Tbilisi State Medical University Tbilisi Georgia

5. University College London, Queen Square Institute of Neurology London UK

Abstract

Parkinson's disease (PD) is a global health challenge, yet historically studies of PD have taken place predominantly in European populations. Recent genetics research conducted in non‐European populations has revealed novel population‐specific genetic loci linked to PD risk, highlighting the importance of studying PD globally. These insights have broadened our understanding of PD etiology, which is crucial for developing disease‐modifying interventions. This review comprehensively explores the global genetic landscape of PD, emphasizing the scientific rationale for studying underrepresented populations. It underscores challenges, such as genotype–phenotype heterogeneity and inclusion difficulties for non‐European participants, emphasizing the ongoing need for diverse and inclusive research in PD. ANN NEUROL 2024;95:831–842

Funder

National Institute on Aging

Publisher

Wiley

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