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Association between plasminogen activator inhibitor-1 gene polymorphisms and susceptibility to Parkinson’s disease in Chinese patients

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Abstract

Purpose

Parkinson’s disease (PD) is a neurodegenerative disease that usually leads to memory impairment, cognitive decline and dementia. Previous studies have reported that plasminogen activator inhibitor-1 (PAI-1) gene polymorphisms play important roles in cardiovascular diseases, obesity, inflammation and other diseases. However, the role of PAI-1 in the diagnosis of Parkinson's disease has not been reported so far.

Methods

This study was a case–control study. This study included 131 PD patients and 97 healthy volunteers. polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) was used to analyze the polymorphic loci of five different regions in PAI-1 gene (rs2227631, rs1799889, rs6092, rs2227694 and rs7242). 60 PD patients and 60 healthy volunteers were selected to detect the plasma PAI-1 concentration. The allele and genotype frequencies of SNPs were assessed using the SHEsis program.

Results

We found that GG genotype frequency and G allele frequency of rs2227631 was significantly higher in the PD patients. Statistically significant difference for rs1799889 could be observed in overdominant model. In subgroup analysis, a significant difference in genotype frequency distribution and allele frequency was found for rs2227631 and rs1799889 between early-onset PD group and the control group. For cognitive dysfunction, the subcomponent showed that GG genotype frequency and G allele frequency of rs2227631 was significantly higher in normal cognition group. The codominant model of rs1799889 was significantly different between the cognitive impairment group and the control group. In addition, the expression of PAI-1 in plasma of PD patients was significantly higher than that of controls, and further analysis showed that the expression of PAI-1 in patients with cognitive impairment was significantly higher than that in patients with cognitive normal.

Conclusion

Our results indicate that the PAI-1 gene rs2227631 and rs1799889 polymorphisms were significantly associated with PD susceptibility in the Chinese Han population. PAI-1 has the potential to become a new therapeutic target and diagnostic marker.

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Availability of data and material

The data used to support the findings of this study are available from the corresponding author upon reasonable request.

Code availability

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Acknowledgements

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Funding

This work was supported by the Basic Research Project of Zhejiang Provincial Department of Science and Technology (2018C37132), the Key Provincial Ministry Joint Construction Program of Zhejiang Provincial Health Commission (WKJ-ZJ-1809).

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Authors and Affiliations

Authors

Contributions

QX and SQ conceived and designed the experiments and revised the manuscript. QL, JW, LZ, LC and YM did genetic analyzes and collected the clinical data. LL, ZZ, YZ and SW analyzed and interpreted the data; and drafted the manuscript. All authors were involved in the revision of the manuscript.

Corresponding author

Correspondence to Song Qiao.

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All authors report no declarations of interest.

Ethics approval

The study was designed and performed in agreement with the Declaration of Helsinki and was approved by Medical Ethics Committee of Zhejiang Hospital (Approval number: 2018(14K)). Written informed consent was obtained from individual or guardian participants.

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Xu, Q., Lai, Q., Wang, J. et al. Association between plasminogen activator inhibitor-1 gene polymorphisms and susceptibility to Parkinson’s disease in Chinese patients. Acta Neurol Belg 122, 1557–1566 (2022). https://doi.org/10.1007/s13760-021-01843-7

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  • DOI: https://doi.org/10.1007/s13760-021-01843-7

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