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10.1016/j.vph.2021.106857

http://scihub22266oqcxt.onion/10.1016/j.vph.2021.106857
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33746068!7970796!33746068
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suck abstract from ncbi

pmid33746068      Vascul+Pharmacol 2021 ; 138 (?): 106857
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  • A possible role for ST2 as prognostic biomarker for COVID-19 #MMPMID33746068
  • Ragusa R; Basta G; Del Turco S; Caselli C
  • Vascul Pharmacol 2021[Jun]; 138 (?): 106857 PMID33746068show ga
  • COVID-19 is a pandemic illness caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2). It has been estimated that 80% of subject infected are asymptomatic or have mild to moderate symptoms. Differently, in severe cases of COVID-19, cytokine storm, acute respiratory distress syndrome (ARDS), severe systemic inflammatory response and cardiovascular diseases were observed Even if all molecular mechanisms leading to cardiovascular dysfunction in COVID-19 patients remain to be clarified, the evaluation of biomarkers of cardiac injury, stress and inflammation proved to be an excellent tool to identify the COVID-19 patients with worse outcome. However, the number of biomarkers used to manage COVID-19 patients is expected to increase with the increasing knowledge of the pathophysiology of the disease. It is our view that soluble suppressor of tumorigenicity 2 (sST2) can be used as biomarker in COVID-19. sST2 is routinely used as prognostic biomarker in patients with HF. Moreover, high circulating levels of sST2 have also been found in subjects with ARDS, pulmonary fibrosis and sepsis. Keeping in mind these considerations, in this review the possible mechanisms through which the SARS-CoV2 infection could damage the cardiovascular system were summarized and the possible role of sST2 in COVID-19 patients with CVD was discussed.
  • |Animals[MESH]
  • |Biomarkers/metabolism[MESH]
  • |COVID-19/diagnosis/*epidemiology/*metabolism[MESH]
  • |Cardiovascular Diseases/diagnosis/epidemiology/metabolism[MESH]
  • |Cytokine Release Syndrome/diagnosis/*epidemiology/*metabolism[MESH]
  • |Humans[MESH]
  • |Interleukin-1 Receptor-Like 1 Protein/*metabolism[MESH]


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