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.