Association between CSF1 and CSF1R Polymorphisms and Parkinson's Disease in Taiwan.

Autor: Chang, Kuo-Hsuan, Wu, Yih-Ru, Chen, Yi-Chun, Wu, Hsiu-Chuan, Chen, Chiung-Mei
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Zdroj: Journal of Clinical Medicine; Oct2019, Vol. 8 Issue 10, p1529, 1p
Abstrakt: Background: CSF1/CSF1R neuroinflammatory signaling is emerging as an important pathway involved in the pathogenesis of Parkinson's disease (PD). However, the genetic associations between CSF1/CSF1R and PD have not yet been explored. Methods: We investigated the effects of two functional genetic variants, including CSF1 rs1058885 and CSF1R rs10079250 in a cohort including 502 Taiwanese patients with PD and 511 age- and gender-matched healthy controls. Results: The CSF1 rs1058885 TT genotype was less frequent in PD patients compared with control subjects (odds ratio (OR) = 0.63, 95% confidence interval (CI): 0.43–0.92, p = 0.015). The PD patients also had a lower frequency of the CSF1 rs1058885 T allele compared with the control subjects (OR = 0.80, 95% CI: 0.67–0.96, p = 0.014). No statistically significant differences in allelic and genotypic frequencies of CSF1R rs10079250 between the PD and control subjects were found, even after stratification by age at onset and gender. Conclusion: This study reports a genetic association between CSF1 and PD for the first time. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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