High levels of von Willebrand factor with reduced specific activities in hospitalized patients with or without COVID-19

The COVID-19 pandemic is often accompanied by severe respiratory illness and thrombotic complications. Von Willebrand Factor (VWF) levels are highly elevated in this condition. However, limited data are available on the qualitative activity of VWF in COVID-19. We measured plasma VWF levels quantitatively (VWF antigen) and qualitatively (ristocetin-induced platelet agglutination, glycoprotein IbM (GPIbM) binding, and collagen binding). Consistent with prior reports, VWF antigen levels were significantly elevated in hospitalized patients with or without COVID-19. The GPIbM and collagen binding activity-to-antigen ratios were significantly reduced, consistent with qualitative changes in VWF in COVID-19. Of note, critically ill hospitalized patients without COVID-19 had similar reductions in VWF activity-to-antigen ratios as patients with COVID-19. Our data suggest that qualitative changes in VWF in COVID-19 may not be specific to COVID-19. Future studies are warranted to determine the mechanisms responsible for qualitative changes in VWF in COVID-19 and other critical illnesses. center dot VWF levels were increased in COVID-19 compared to healthy controls. center dot VWF activity-to-antigen ratios were decreased in COVID-19 compared to healthy controls. center dot There were no differences in VWF activity-to-antigen ratios between hospitalized patients with or without COVID-19. center dot These findings are consistent with qualitative changes in VWF in systemic inflammation which are not specific to COVID-19. center dot Future studies are needed to define possible roles of changes in conformation or multimer length in the qualitative changes in VWF in systemic inflammation.

Automated summary

COVID-19 is associated with changes in the activity and quality of VWF, but these changes are not specific to COVID-19. Similar changes in VWF activity and quality are observed in hospitalized patients with or without COVID-19. Further research is needed to understand the mechanisms responsible for qualitative changes in VWF in COVID-19 and other critical illnesses.