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Association of RAGE gene polymorphisms with sporadic Parkinson's disease in Chinese Han population
Jing Gao1, Jijun Teng1, Hongxin Liu1
1Department of Neurology, Affiliated Hospital of Medical College, Qingdao University, Qingdao, China.
Abstract:
Previous studies have corroborated receptor for advanced glycation end-products (RAGE) ablation had a protective effect on nigral dopaminergic neurons in the MPTP model of Parkinson's disease (PD). Genetic variation of RAGE gene may be associated with the development of onset of sporadic PD. The present study aimed to explore the possible association of RAGE gene polymorphisms namely -374T/A,-429T/C, and G82S with PD. A total of 285 PD patients and 285 healthy-matched individuals in Chinese Han population were enrolled. Genotype analyses were performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Only the -429T/C polymorphism denoted a significant difference between PD patients and controls (P=0.015) of the three examined single nucleotide polymorphisms (SNPs). Our data also revealed that -429C allele carriers seem to have a decreased risk of PD (OR=0.617, P=0.007). Moreover, there were significant differences in genotype distribution in female PD group and its healthy-matched control subgroup (P=0.014), as well as between late-onset PD (LOPD) and the controls subgroup (P=0.016). However, for -374T/A and 82GS polymorphisms, there was no significant difference in the genotype and allele frequencies between PD patients and the controls, as well as gender- and age-related differences. Our present findings indicate that the RAGE -429T/C polymorphism may be associated with the susceptibility of PD and the CC genotype of -429T/C may be a protective factor for PD in Chinese Han population.
Insights
The RAGE -429T/C gene polymorphism may be linked to Parkinson's disease (PD) susceptibility. Specifically, the CC genotype appears to offer protection against PD in the Chinese Han population.
Area of Science:
- Neuroscience
- Genetics
- Epidemiology
Background:
- Receptor for advanced glycation end-products (RAGE) ablation shows protective effects on dopaminergic neurons in Parkinson's disease (PD) models.
- Genetic variations in the RAGE gene are potentially linked to the development of sporadic PD.
- Investigating RAGE gene polymorphisms offers insights into PD pathogenesis.
Purpose of the Study:
- To explore the association between RAGE gene polymorphisms (-374T/A, -429T/C, G82S) and Parkinson's disease (PD).
- To determine if specific RAGE single nucleotide polymorphisms (SNPs) influence PD risk in the Chinese Han population.
- To examine potential gender and age-related differences in RAGE polymorphism associations with PD.
Main Methods:
- Case-control study involving 285 PD patients and 285 healthy controls from the Chinese Han population.
- Genotyping performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) for RAGE gene polymorphisms.
- Statistical analyses to compare genotype and allele frequencies between PD patients and controls, including subgroup analyses for gender and late-onset PD.
Main Results:
- The RAGE -429T/C polymorphism showed a significant difference between PD patients and controls (P=0.015).
- -429C allele carriers exhibited a decreased risk of PD (OR=0.617, P=0.007).
- Significant genotype distribution differences were observed in female PD patients and late-onset PD (LOPD) subgroups compared to controls.
Conclusions:
- The RAGE -429T/C polymorphism is associated with PD susceptibility in the Chinese Han population.
- The CC genotype of the RAGE -429T/C polymorphism may act as a protective factor against PD.
- Further research is warranted to elucidate the role of RAGE in PD pathogenesis and explore other RAGE polymorphisms.
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