When type II diabetes mellitus meets COVID-19-Identification of the shared gene signatures and biological mechanism between the two diseases

Eur J Clin Invest. 2023 May;53(5):e13955. doi: 10.1111/eci.13955. Epub 2023 Jan 31.

Abstract

Background: According to current studies, more than 20% of all patients diagnosed with COVID-19 globally have diabetes. Further, the mortality rate of these patients is 7.3%. Compared with non-diabetic COVID-19 patients, diabetic COVID-19 patients have higher rates of mortality and severe infection, suggesting that diabetes is associated with the severity of COVID-19 infection. This study aimed to analyse the relationship and susceptibility factors between COVID-19 and T2DM.

Methods: Using bioinformatics methods, potential targets for COVID-19 and T2DM were screened from GeneCards database. Potential targets of COVID-19 and T2DM were mapped to each other to identify overlapping targets, and a PPI network was constructed to extract the core target. The clusterProfiler package in R was used to analyse the function and pathway that core target involved. GO enrichment and KEGG pathway analysis were used to elucidate the correlation between COVID-19 and T2DM.

Results: A total of 277 potential pathogenic targets of COVID-19 were found, 282 potential targets were found for T2DM. Mapping of the potential COVID-19 and T2DM targets revealed 53 overlapping targets, with TNF as the core target. IL-17 signalling pathway was the most significant KEGG pathway involving TNF.

Conclusions: The inflammatory cytokine, TNF, was identified as a core target between COVID-19 and T2DM, which induces inflammatory response mainly through the IL-17 signalling pathway, leading to aggravation of infection and increased difficulty in blood glucose control. This study provides a reference for further exploring the potential correlation and endogenous mechanisms between two seemingly independent and unrelated diseases-T2DM and COVID-19.

Keywords: COVID-19; IL-17 signalling pathway; T2DM; correlation mechanism; shared gene signatures.

MeSH terms

  • COVID-19*
  • Computational Biology
  • Cytokines
  • Diabetes Mellitus, Type 2* / genetics
  • Drugs, Chinese Herbal*
  • Humans
  • Interleukin-17
  • Molecular Docking Simulation

Substances

  • Interleukin-17
  • Cytokines
  • Drugs, Chinese Herbal