Study on the correlation between DPP9 rs2109069 and IFNAR2 rs2236757 polymorphisms with COVID-19 mortality
Mahnaz Safari1, Rezvan Tavakoli2, Mohammadreza Aghasadeghi2,3
1Department of Biology, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Insights
Genetic variations in dipeptidylpeptidase 9 (DPP9) and interferon alpha and beta receptor subunit 2 (IFNAR2) genes impact COVID-19 severity. The IFNAR2 A allele correlates with milder disease, while the DPP9 A allele is linked to increased mortality.
Area of Science:
- Immunogenetics
- Molecular Biology
- Infectious Disease Research
Background:
- COVID-19 severity is influenced by the immune system's pro-inflammatory response.
- Cytokine and chemokine gene polymorphisms may play a role in COVID-19 outcomes.
Purpose of the Study:
- To investigate the association between single nucleotide polymorphisms (SNPs) in DPP9 and IFNAR2 genes and COVID-19 severity.
- To determine if specific genetic variants correlate with disease outcomes in COVID-19 patients.
Main Methods:
- Utilized polymerase chain reaction with restriction fragment length polymorphism (PCR-RFLP) assay.
- Analyzed 954 COVID-19 patients (528 recovered, 426 deceased).
- Examined polymorphisms in IFNAR2 (rs2236757) and DPP9 (rs2109069).
Main Results:
- The IFNAR2 rs2236757 A allele was associated with reduced COVID-19 severity.
- The DPP9 rs2109069 A allele frequency was higher in deceased patients compared to recovered patients.
- Carrying the DPP9 G allele and IFNAR2 A allele correlated with significantly better disease recovery.
Conclusions:
- IFNAR2 rs2236757 A allele is linked to decreased COVID-19 severity.
- DPP9 rs2109069 A allele frequency is higher in non-survivors, suggesting a role in COVID-19 mortality.
- Genetic variants in inflammatory response genes like DPP9 and IFNAR2 are crucial in determining COVID-19 severity.
Abstract:
Understanding the complex mechanisms of the immune system in dealing with the COVID-19 infection, which is probably related to the polymorphism in cytokine and chemokine genes, can explain the pro-inflammatory condition of patients. Therefore, in this study, the relationship between the frequency of single nucleotide polymorphisms in the two pro-inflammatory genes dipeptidylpeptidase 9 (DPP9) and interferon alpha and beta receptor subunit 2 (IFNAR2) and the severity of COVID-19 was assessed. This study involved 954 COVID-19 patients, including 528 recovered and 426 deceased patients. To investigate the polymorphisms of IFNAR2 rs2236757 and DPP9 rs2109069, we used the polymerase chain reaction with the restriction fragment length polymorphism assay. The results showed that IFNAR2 rs2236757 A allele is related to the reduced severity of the disease, whereas the incidence of DPP9 rs2109069 A allele was higher among the deceased than recovered individuals. On the other hand, in people carrying the G allele in the DPP9 gene polymorphism and the allele A in the IFNR2 gene polymorphism, the improvement of the disease was significantly higher. In conclusion, the results showed that IFNAR2 rs2236757 A allele is related to the decrease in the severity of the disease, while the frequency of DPP9 rs2109069 A allele was higher in deceased people than in recovered people. This shows the important role of genes related to inflammatory responses as well as the role of genetic variants of these genes in the severity of COVID-19.
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