VEGFR and DPP-IV as Markers of Severe COVID-19 and Predictors of ICU Admission.
Ewa Pius-SadowskaPiotr KuligAnna NiedźwiedźBartłomiej BaumertKarolina ŁuczkowskaDorota RogińskaAnna SobuśZofia UlańczykMiłosz KawaEdyta PaczkowskaMiłosz ParczewskiAnna MachalińskaBogusław MachalińskiPublished in: International journal of molecular sciences (2023)
The pathophysiology of the severe course of COVID-19 is multifactorial and not entirely elucidated. However, it is well known that the hyperinflammatory response and cytokine storm are paramount events leading to further complications. In this paper, we investigated the vascular response in the pathophysiology of severe COVID-19 and aimed to identify novel biomarkers predictive of ICU admission. The study group consisted of 210 patients diagnosed with COVID-19 (age range: 18-93; mean ± SD: 57.78 ± 14.16), while the control group consisted of 80 healthy individuals. We assessed the plasma concentrations of various vascular factors using the Luminex technique. Then, we isolated RNA from blood mononuclear cells and performed a bioinformatics analysis investigating various processes related to vascular response, inflammation and angiogenesis. Our results confirmed that severe COVID-19 is associated with vWF/ADAMTS 13 imbalance. High plasma concentrations of VEGFR and low DPP-IV may be potential predictors of ICU admission. SARS-CoV-2 infection impairs angiogenesis, hinders the generation of nitric oxide, and thus impedes vasodilation. The hypercoagulable state develops mainly in the early stages of the disease, which may contribute to the well-established complications of COVID-19.
Keyphrases
- coronavirus disease
- sars cov
- nitric oxide
- respiratory syndrome coronavirus
- emergency department
- intensive care unit
- end stage renal disease
- vascular endothelial growth factor
- chronic kidney disease
- induced apoptosis
- oxidative stress
- endothelial cells
- risk factors
- newly diagnosed
- signaling pathway
- peritoneal dialysis
- drug induced
- prognostic factors
- risk assessment
- cell cycle arrest
- acute respiratory distress syndrome
- cell proliferation
- patient reported outcomes
- nucleic acid
- nitric oxide synthase