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Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson’s Disease Progression

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Abstract

Parkinson’s disease (PD) is a chronic neurodegenerative disease that has relatively slow progression with motor symptoms. Leucine-rich repeat kinase 2 (LRRK2) gene mutations and polymorphisms are suggested to be associated with PD. In this study, we aimed to investigate the association between single-nucleotide polymorphisms (SNPs) of the LRRK2 gene, namely, rs11176013, rs10878371, rs11835105, and PD. Genotypes of 132 PD cases and 133 healthy individuals were determined by qRT-PCR. Haplotype analysis was performed. Additionally, LRRK2 mRNA expression levels were determined in 83 PD cases and 55 healthy subjects. The relationship between LRRK2 mRNA levels, the target SNPs, and clinical data was also investigated. Our results indicated that the “GG” genotype and “G” allele of rs11176013 and the “CC” genotype and “C” allele of rs10878371 were more frequent in cases. The “GCG” haplotype was significantly more frequent in cases. LRRK2 mRNA expression levels in patients were significantly lower than those in healthy individuals. The patients with the “CC” genotype for rs10878371 and the “GG” genotype for rs11176013 had decreased LRRK2 mRNA levels. We found that the rs11176013 “GG” genotype and the rs10878371 “CC” genotype were less frequently seen in cases with akinetic rigid or combined akinetic rigid and tremor-dominant initial symptoms. Consequently, our results demonstrate that the rs11176013 and rs10878371 polymorphisms are associated with PD in a Turkish cohort, and moreover, these results suggest that these polymorphisms may affect the expression of the LRRK2 gene and disease progression and thus play a role in the pathogenesis of PD.

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Acknowledgements

The present work was supported by the Research Fund of Istanbul University-Cerrahpasa. Project Nos. 58745, 27781, 26989. The English of the manuscript has been edited by American Journal Experts (AJE) Language Editing Service with the Reference Number 36C1-0FDB-3704-D03B-B8D5.

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Conceptualization: DGA, SE, ED; Data Curation: EC, DGA, MA, BŞ, GG, AG, HA, GK, SE, ED; Formal Analysis: DGA, EC, ED; Funding Acquisition: SY; Investigation: SY, EC, DGA, ED; Methodology: DGA, EC, MA, GG, BŞ, SY, SE, ED; Project Administration: SY, DGA, ED; Resources; SY, DGA, ED; Supervision: SY, SE, DGA, ED; Validation: DGA, ED; Writing—Original Draft Preparation: DGA, ED; Writing—Review & Editing: DGA, SY, SE, ED. All authors read and approved the final manuscript.

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Correspondence to Selma Yılmazer.

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The authors declare that they have no conflict of interest.

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Participants in the present study were treated according to the ethical principles for medical research involving human participants described in the World Medical Association’s Declaration of Helsinki, and the study was approved by the Ethics Committee of Istanbul University.

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Signed informed consent was obtained from all study participants.

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Yılmazer, S., Candaş, E., Genç, G. et al. Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson’s Disease Progression. Neuromol Med 23, 292–304 (2021). https://doi.org/10.1007/s12017-020-08619-x

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  • DOI: https://doi.org/10.1007/s12017-020-08619-x

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