qrhz4is

Property	Value
?:abstract	RATIONALE: Pre-clinical and autopsy studies have fueled the hypothesis that a dysregulated vascular endothelium might play a central role in the pathogenesis of ARDS and multi-organ failure in COVID-19. OBJECTIVES: To comprehensively characterize and quantify microvascular alterations in patients with COVID-19. METHODS: Hospitalized adult patients with moderate-to-severe or critical COVID-19 (n = 23) were enrolled non-consecutively in this prospective, observational, cross-sectional, multi-center study. Fifteen healthy volunteers served as controls. All participants underwent intravital microscopy by sidestream dark field imaging to quantify vascular density, red blood cell velocity (V(RBC)), and glycocalyx dimensions (perfused boundary region, PBR) in sublingual microvessels. Circulating levels of endothelial and glycocalyx-associated markers were measured by multiplex proximity extension assay and enzyme-linked immunosorbent assay. MEASUREMENTS AND MAIN RESULTS: COVID-19 patients showed an up to 90% reduction in vascular density, almost exclusively limited to small capillaries (diameter 4–6 µm), and also significant reductions of V(RBC). Especially, patients on mechanical ventilation showed severe glycocalyx damage as indicated by higher PBR values (i.e., thinner glycocalyx) and increased blood levels of shed glycocalyx constituents. Several markers of endothelial dysfunction were increased and correlated with disease severity in COVID-19. PBR (AUC 0.75, p = 0.01), ADAMTS13 (von Willebrand factor-cleaving protease; AUC 0.74, p = 0.02), and vascular endothelial growth factor A (VEGF-A; AUC 0.73, p = 0.04) showed the best discriminatory ability to predict 60-day in-hospital mortality. CONCLUSIONS: Our data clearly show severe alterations of the microcirculation and the endothelial glycocalyx in patients with COVID-19. Future therapeutic approaches should consider the importance of systemic vascular involvement in COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10456-020-09753-7) contains supplementary material, which is available to authorized users.
is ?:annotates of	<https://research.tib.eu/covid-19/entity/0qrhz4is_hasAnnotation_C0026766> <https://research.tib.eu/covid-19/entity/0qrhz4is_hasAnnotation_C1823521> <https://research.tib.eu/covid-19/entity/0qrhz4is_hasAnnotation_C1823619>
?:creator	<https://research.tib.eu/covid-19/entity/Rovas%2C_Alexandros%3B_Osiaevi%2C_Irina%3B_Buscher%2C_Konrad%3B_Sackarnd%2C_Jan%3B_Tepasse%2C_Phil-Robin%3B_Fobker%2C_Manfred%3B_K%C3%BChn%2C_Joachim%3B_Braune%2C_Stephan%3B_G%C3%B6bel%2C_Ulrich%3B_Th%C3%B6lking%2C_Gerold%3B_Gr%C3%B6schel%2C_Andreas%3B_Pavenst%C3%A4dt%2C_Hermann%3B_Vink%2C_Hans%3B_K%C3%BCmpers%2C_Philipp>
?:doi	10.1007/s10456-020-09753-7
?:doi	<https://research.tib.eu/covid-19/entity/10.1007/s10456-020-09753-7>
?:journal	Angiogenesis
?:license	cc-by
?:pdf_json_files	document_parses/pdf_json/78efa54d7af7ef7acae1ab1c0179358a59fe6b82.json
?:pmc_json_files	document_parses/pmc_json/PMC7556767.xml.json
?:pmcid	<https://research.tib.eu/covid-19/entity/PMC7556767>
?:pmid	<https://research.tib.eu/covid-19/entity/33058027.0>
?:pmid	33058027.0
?:publication_isRelatedTo_Disease	<https://research.tib.eu/covid-19/entity/COVID-19>
is ?:relation_isRelatedTo_publication of	<https://research.tib.eu/covid-19/entity/0qrhz4is_HAS_C0026766_COEXISTS_WITH_C5203670> <https://research.tib.eu/covid-19/entity/0qrhz4is_HAS_C0035222_COEXISTS_WITH_C5203670> <https://research.tib.eu/covid-19/entity/0qrhz4is_HAS_C0856169_COEXISTS_WITH_C5203670>
?:sha_id	<https://research.tib.eu/covid-19/entity/78efa54d7af7ef7acae1ab1c0179358a59fe6b82>
?:source	Medline; PMC
?:title	Microvascular dysfunction in COVID-19: the MYSTIC study
?:type	<https://research.tib.eu/covid-19/vocab/Publication>
?:year	2020-10-14

Property

Value

?:abstract

RATIONALE: Pre-clinical and autopsy studies have fueled the hypothesis that a dysregulated vascular endothelium might play a central role in the pathogenesis of ARDS and multi-organ failure in COVID-19. OBJECTIVES: To comprehensively characterize and quantify microvascular alterations in patients with COVID-19. METHODS: Hospitalized adult patients with moderate-to-severe or critical COVID-19 (n = 23) were enrolled non-consecutively in this prospective, observational, cross-sectional, multi-center study. Fifteen healthy volunteers served as controls. All participants underwent intravital microscopy by sidestream dark field imaging to quantify vascular density, red blood cell velocity (V(RBC)), and glycocalyx dimensions (perfused boundary region, PBR) in sublingual microvessels. Circulating levels of endothelial and glycocalyx-associated markers were measured by multiplex proximity extension assay and enzyme-linked immunosorbent assay. MEASUREMENTS AND MAIN RESULTS: COVID-19 patients showed an up to 90% reduction in vascular density, almost exclusively limited to small capillaries (diameter 4–6 µm), and also significant reductions of V(RBC). Especially, patients on mechanical ventilation showed severe glycocalyx damage as indicated by higher PBR values (i.e., thinner glycocalyx) and increased blood levels of shed glycocalyx constituents. Several markers of endothelial dysfunction were increased and correlated with disease severity in COVID-19. PBR (AUC 0.75, p = 0.01), ADAMTS13 (von Willebrand factor-cleaving protease; AUC 0.74, p = 0.02), and vascular endothelial growth factor A (VEGF-A; AUC 0.73, p = 0.04) showed the best discriminatory ability to predict 60-day in-hospital mortality. CONCLUSIONS: Our data clearly show severe alterations of the microcirculation and the endothelial glycocalyx in patients with COVID-19. Future therapeutic approaches should consider the importance of systemic vascular involvement in COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10456-020-09753-7) contains supplementary material, which is available to authorized users.

is ?:annotates of