A Mendelian randomization study of genetic predisposition to autoimmune diseases and COVID-19

Sci Rep. 2022 Oct 21;12(1):17703. doi: 10.1038/s41598-022-22711-1.

Abstract

Autoimmune diseases and coronavirus disease 2019 (COVID-19) share many similarities. Concerns have arisen that autoimmune diseases may increase the susceptibility and severity of COVID-19. We used Mendelian randomization to investigate whether liability to autoimmune diseases is related to COVID-19 susceptibility and severity. Genetic instruments for 8 autoimmune diseases, including type 1 diabetes mellitus, rheumatoid arthritis, systemic lupus erythematosus, psoriasis, multiple sclerosis, primary sclerosing cholangitis, primary biliary cirrhosis and juvenile idiopathic arthritis, were obtained from published genome-wide association studies. Two-sample Mendelian randomization analyses of the associations of liability to each autoimmune disease with COVID-19 infection, hospitalized COVID-19, and very severe COVID-19 were performed using the latest publicly available genome-wide association study for COVID-19. Genetic liability to each of the autoimmune diseases was largely not associated with COVID-19 infection, hospitalized COVID-19, or very severe COVID-19 after accounting for multiple comparison. Sensitivity analysis excluding genetic variants in the human leukocyte antigen gene, which has an important role in the immune response, showed similar results. The autoimmune diseases examined were largely not genetically associated with the susceptibility or severity of COVID-19. Further investigations are warranted.

MeSH terms

  • Arthritis, Juvenile* / genetics
  • Autoimmune Diseases* / epidemiology
  • Autoimmune Diseases* / genetics
  • COVID-19* / epidemiology
  • COVID-19* / genetics
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • HLA Antigens
  • Humans
  • Mendelian Randomization Analysis
  • Polymorphism, Single Nucleotide

Substances

  • HLA Antigens