RAB32 Ser71Arg in Chinese patients with Parkinson's disease
- PMID: 39652162
- DOI: 10.1007/s10072-024-07910-0
RAB32 Ser71Arg in Chinese patients with Parkinson's disease
Abstract
Background: The RAB32 Ser71Arg variant has been identified as a novel risk locus for Parkinson's disease (PD) in North American, European and North African populations. However, its pathogenicity in Asian populations remains unclear.
Method: To investigate this, we screened for the RAB32 c.213C > G (Ser71Arg) variant using Sanger sequencing in 1,099 PD patients and 1,549 controls. And we search for the RAB32 Ser71Arg variant in public databases to identified its mutant frequency.
Results: Our results show that no individuals carrying the RAB32 Ser71Arg variant were identified in our cohort. Additionally, this variant rarely appears in Asian population databases.
Conclusion: Our findings suggest that the RAB32 Ser71Arg variant is unlikely to be a risk locus for PD in Chinese patients, which is potentially attributed to racial or ethnic differences.
Keywords: Chinese populations; Genetics; Parkinson’s disease; RAB32.
© 2024. Fondazione Società Italiana di Neurologia.
Conflict of interest statement
Declarations. Ethical compliance statement: The study was approved by the ethics committee of the First Affiliated Hospital of Zhengzhou University (No.2019-KY-294). Conflict of interest: We declare no competing interests. Informed consent: Written informed consent was obtained from all study participants before enrollment.
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- U1904207/the National Natural Science Foundation of China
- 82171434/the National Natural Science Foundation of China
- 92249305/the National Natural Science Foundation of China
- 2020-PT310-01/the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences
- 222300420070/the Excellent youth project of Henan Provincial Natural Science Foundation
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