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Association Analyses of SNAP25, HNMT, FCHSD1 , and DBH Single-Nucleotide Polymorphisms with Parkinson's Disease in a Northern Chinese Population
Sequencing potentially causal and susceptible genes and genome-wide association studies in samples from Parkinson's disease (PD) patients has revealed several related loci. The genes for synaptosome-associated protein of 25 kDa (SNAP25), histamine-N-methyltransferase (HNMT), FCH and double SH3...
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Published in: | Neuropsychiatric disease and treatment 2021-01, Vol.17, p.1689-1695 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Sequencing potentially causal and susceptible genes and genome-wide association studies in samples from Parkinson's disease (PD) patients has revealed several related loci. The genes for synaptosome-associated protein of 25 kDa (SNAP25), histamine-N-methyltransferase (HNMT), FCH and double SH3 domains 1 (FCHSD1) and dopamine β-hydroxylase (DBH) are candidate loci and have not been studied in a northern Chinese population. We explored the genetic distribution of four single-nucleotide polymorphisms (rs3746544, rs11558538, rs456998, rs129882) located on
and
, respectively.
A total of 330 patients with sporadic PD and 332 healthy controls (HCs) were recruited from a northern Chinese population. Polymerase chain reaction restriction fragment length polymorphism was used to genotype these four SNPs.
After statistical analyses and correction of the genotyping results, the mutant-allele T in rs456998 of
was found to be significantly related to reducing the PD risk (
= 0.029, OR = 0.754, 95% CI = 0.586-0.971, power = 0.591). However, rs3746544, rs11558538, and rs129882 did not show an association with PD.
rs456998 may have a protective role in PD in a northern Chinese population, but more studies are needed to support this suggestion. |
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ISSN: | 1176-6328 1178-2021 1178-2021 |
DOI: | 10.2147/NDT.S304062 |