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Article 2021 · 24 atıf

Evaluation of the relationship between KIM-1 and suPAR levels and clinical severity in COVID-19 patients: A different perspective on suPAR

Kerget, Bugra, Kerget, Ferhan, Aksakal, Alperen, Askin, Seda, Ucar, Elif Yilmazel, Saglam, Leyla

Özet

Coronavirus disease 2019 (COVID-19) is one of the most pressing health problems of this century, but our knowledge of the disease is still limited. In this study, we aimed to examine serum-soluble urokinase plasminogen activator receptor (suPAR) and kidney injury molecule 1 (KIM-1) levels based on the clinical course of COVID-19. Our study included 102 patients over the age of 18 who were diagnosed as having COVID-19 between September 2020 and December 2020 and a control group of 50 health workers over the age of 18 whose severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) PCR results were negative. KIM-1 was measured by ELISA and suPAR by suPARnostic (TM) assay. Analysis of previously identified variables of prognostic significance in COVID-19 revealed high neutrophil to lymphocyte ratio, lactose dehydrogenase, prothrombin time, C-reactive protein, PaO2/FiO(2), D-dimer, ferritin, and fibrinogen levels in patients with severe disease (p < 0.05 for all). KIM-1 and suPAR levels were significantly higher in COVID-19 patients compared to the control group (p = 0.001 for all). KIM-1 level was higher in severe patients compared to moderate patients (p = 0.001), while suPAR level was lower (p = 0.001). KIM-1, which is believed to play an important role in the endocytosis of SARS-CoV-2, was elevated in patients with severe COVID-19 and may be a therapeutic target in the future. SuPAR may have a role in defense mechanism and fibrinolysis, and low levels in severe patients may be associated with poor prognosis in the early period.

Anahtar Kelimeler
COVID-19 KIM-1 suPAR PLASMINOGEN-ACTIVATOR RECEPTOR
WoS Kategorileri
Virology
Sürdürülebilir Kalkınma Amaçları
Künye
Dergi
JOURNAL OF MEDICAL VIROLOGY
Yıl
2021
Cilt
93
Sayı
9
Sayfa
5568-5573
ISSN
0146-6615
eISSN
1096-9071
DOI
10.1002/jmv.27099
WoS UID
WOS:000655693800001
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