TOMÁŠKOVÁ, Veronika, Alexandra MÝTNIKOVÁ, Marcela HORTOVÁ KOHOUTKOVÁ, Ondřej MRKVA, Monika SKOTÁKOVÁ, Michal ŠITINA, Kateřina HELÁNOVÁ, Jan FRIČ, Jiří PAŘENICA, Vladimír ŠRÁMEK and Martin HELÁN. Prognostic value of soluble endoglin in patients with septic shock and severe COVID-19. Frontiers in Medicine. Laussane: Frontiers, 2022, vol. 9, August 2022, p. 1-10. ISSN 2296-858X. Available from: https://dx.doi.org/10.3389/fmed.2022.972040.
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Basic information
Original name Prognostic value of soluble endoglin in patients with septic shock and severe COVID-19
Authors TOMÁŠKOVÁ, Veronika (203 Czech Republic, belonging to the institution), Alexandra MÝTNIKOVÁ (703 Slovakia, belonging to the institution), Marcela HORTOVÁ KOHOUTKOVÁ (203 Czech Republic), Ondřej MRKVA (203 Czech Republic), Monika SKOTÁKOVÁ (203 Czech Republic), Michal ŠITINA (203 Czech Republic, belonging to the institution), Kateřina HELÁNOVÁ (203 Czech Republic, belonging to the institution), Jan FRIČ (203 Czech Republic), Jiří PAŘENICA (203 Czech Republic, belonging to the institution), Vladimír ŠRÁMEK (203 Czech Republic, belonging to the institution) and Martin HELÁN (203 Czech Republic, guarantor, belonging to the institution).
Edition Frontiers in Medicine, Laussane, Frontiers, 2022, 2296-858X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30218 General and internal medicine
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.900
RIV identification code RIV/00216224:14110/22:00129697
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3389/fmed.2022.972040
UT WoS 000854438500001
Keywords in English endoglin; COVID-19; sepsis; shock; endothelial dysfunction; biomarker; mortality
Tags 14110122, 14110211, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 1/11/2022 13:50.
Abstract
Sepsis is a clinical syndrome characterized by a dysregulated response to infection. It represents a leading cause of mortality in ICU patients worldwide. Although sepsis is in the point of interest of research for several decades, its clinical management and patient survival are improving slowly. Monitoring of the biomarkers and their combinations could help in early diagnosis, estimation of prognosis and patient's stratification and response to the treatment. Circulating soluble endoglin (sEng) is the cleaved extracellular part of transmembrane glycoprotein endoglin. As a biomarker, sEng has been tested in several pathologic conditions where its elevation was associated with endothelial dysfunction. In this study we have tested the ability of sEng to predict mortality and its correlation with other clinical characteristics in the cohort of septic shock patients (n = 37) and patients with severe COVID-19 (n = 40). In patients with COVID-19 sEng did not predict mortality or correlate with markers of organ dysfunction. In contrast, in septic shock the level of sEng was significantly higher in patients with early mortality (p = 0.019; AUC = 0.801). Moreover, sEng levels correlated with signs of circulatory failure (required dose of noradrenalin and lactate levels; p = 0.002 and 0.016, respectively). The predominant clinical problem in patients with COVID-19 was ARDS, and although they often showed signs of other organ dysfunction, circulatory failure was exceptional. This potentially explains the difference between sEng levels in COVID-19 and septic shock. In conclusion, we have confirmed that sEng may reflect the extent of the circulatory failure in septic shock patients and thus could be potentially used for the early identification of patients with the highest degree of endothelial dysfunction who would benefit from endothelium-targeted individualized therapy.
Links
NU21-06-00408, research and development projectName: Prediktivní potenciál dynamických změn v subpopulacích neutrofilů a monocytů ve vývoji SIRS a sepse po operaci nebo traumatu.
Investor: Ministry of Health of the CR, Subprogram 1 - standard
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