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Evaluation of Soluble Urokinase Plasminogen Activator Receptor in COVID-19 Patients
This retrospective study analyzed soluble urokinase plasminogen activator receptor (suPAR) plasma levels alongside routine inflammatory markers, including the neutrophil-to-lymphocyte count ratio, C-reactive protein (CRP), interleukin-6 (IL-6), procalcitonin (PCT), and D-dimers in COVID-19 patients...
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Published in: | Journal of clinical medicine 2024-10, Vol.13 (21), p.6340 |
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description | This retrospective study analyzed soluble urokinase plasminogen activator receptor (suPAR) plasma levels alongside routine inflammatory markers, including the neutrophil-to-lymphocyte count ratio, C-reactive protein (CRP), interleukin-6 (IL-6), procalcitonin (PCT), and D-dimers in COVID-19 patients hospitalized during the Omicron wave of the pandemic.
We measured plasma suPAR levels using a suPARnostic
Quick Triage kit. We divided COVID-19 patients into two groups based on the severity of SARS-CoV-2 infection according to the National Institutes of Health (NIH) criteria. The logistic regression analysis tested the predictive value of the biomarkers.
We evaluated 160 consecutive COVID-19 patients hospitalized between January and August 2022. The cohort exhibited a high incidence of comorbidities, with an in-hospital mortality rate of 5.6%. Upon admission, the median suPAR plasma levels were not significantly different between patients with mild COVID-19 (n = 110) and those with moderate/severe disease (n = 50), with 7.25 ng/mL and 7.55 ng/mL, respectively. We observed significant differences (
< 0.01) between the groups for CRP and IL-6 levels that were higher in moderate/severe disease than in mild infection. Additionally, suPAR plasma levels were above the normal range (0-2.00 ng/mL) in all patients, with a significant positive correlation identified between suPAR levels and serum IL-6, PCT, and creatinine levels.
These findings indicate that COVID-19 during the Omicron wave is strongly associated with elevated suPAR levels; however, these levels do not directly correlate with the severity of SARS-CoV-2 infection. |
doi_str_mv | 10.3390/jcm13216340 |
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We measured plasma suPAR levels using a suPARnostic
Quick Triage kit. We divided COVID-19 patients into two groups based on the severity of SARS-CoV-2 infection according to the National Institutes of Health (NIH) criteria. The logistic regression analysis tested the predictive value of the biomarkers.
We evaluated 160 consecutive COVID-19 patients hospitalized between January and August 2022. The cohort exhibited a high incidence of comorbidities, with an in-hospital mortality rate of 5.6%. Upon admission, the median suPAR plasma levels were not significantly different between patients with mild COVID-19 (n = 110) and those with moderate/severe disease (n = 50), with 7.25 ng/mL and 7.55 ng/mL, respectively. We observed significant differences (
< 0.01) between the groups for CRP and IL-6 levels that were higher in moderate/severe disease than in mild infection. Additionally, suPAR plasma levels were above the normal range (0-2.00 ng/mL) in all patients, with a significant positive correlation identified between suPAR levels and serum IL-6, PCT, and creatinine levels.
These findings indicate that COVID-19 during the Omicron wave is strongly associated with elevated suPAR levels; however, these levels do not directly correlate with the severity of SARS-CoV-2 infection.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm13216340</identifier><identifier>PMID: 39518479</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Biological markers ; Biomarkers ; Blood ; Care and treatment ; Comorbidity ; COVID-19 ; Creatinine ; Diagnosis ; Disease ; Dosage and administration ; Hospital patients ; Hospitalization ; Hospitals ; Infections ; Laboratories ; Mortality ; Oxygen therapy ; Pandemics ; Patients ; Plasma ; Regression analysis ; Severe acute respiratory syndrome coronavirus 2 ; Urokinase</subject><ispartof>Journal of clinical medicine, 2024-10, Vol.13 (21), p.6340</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c328t-6f6ab978d917d55ee3e32f5d597e9b8acb58543edf0c82289ebdc5d1dde3bd443</cites><orcidid>0000-0003-1894-2605</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3126049291/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3126049291?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39518479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arientová, Simona</creatorcontrib><creatorcontrib>Matúšková, Kateřina</creatorcontrib><creatorcontrib>Bartoš, Oldřich</creatorcontrib><creatorcontrib>Beran, Ondřej</creatorcontrib><creatorcontrib>Holub, Michal</creatorcontrib><title>Evaluation of Soluble Urokinase Plasminogen Activator Receptor in COVID-19 Patients</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>This retrospective study analyzed soluble urokinase plasminogen activator receptor (suPAR) plasma levels alongside routine inflammatory markers, including the neutrophil-to-lymphocyte count ratio, C-reactive protein (CRP), interleukin-6 (IL-6), procalcitonin (PCT), and D-dimers in COVID-19 patients hospitalized during the Omicron wave of the pandemic.
We measured plasma suPAR levels using a suPARnostic
Quick Triage kit. We divided COVID-19 patients into two groups based on the severity of SARS-CoV-2 infection according to the National Institutes of Health (NIH) criteria. The logistic regression analysis tested the predictive value of the biomarkers.
We evaluated 160 consecutive COVID-19 patients hospitalized between January and August 2022. The cohort exhibited a high incidence of comorbidities, with an in-hospital mortality rate of 5.6%. Upon admission, the median suPAR plasma levels were not significantly different between patients with mild COVID-19 (n = 110) and those with moderate/severe disease (n = 50), with 7.25 ng/mL and 7.55 ng/mL, respectively. We observed significant differences (
< 0.01) between the groups for CRP and IL-6 levels that were higher in moderate/severe disease than in mild infection. Additionally, suPAR plasma levels were above the normal range (0-2.00 ng/mL) in all patients, with a significant positive correlation identified between suPAR levels and serum IL-6, PCT, and creatinine levels.
These findings indicate that COVID-19 during the Omicron wave is strongly associated with elevated suPAR levels; however, these levels do not directly correlate with the severity of SARS-CoV-2 infection.</description><subject>Analysis</subject><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Blood</subject><subject>Care and treatment</subject><subject>Comorbidity</subject><subject>COVID-19</subject><subject>Creatinine</subject><subject>Diagnosis</subject><subject>Disease</subject><subject>Dosage and administration</subject><subject>Hospital patients</subject><subject>Hospitalization</subject><subject>Hospitals</subject><subject>Infections</subject><subject>Laboratories</subject><subject>Mortality</subject><subject>Oxygen therapy</subject><subject>Pandemics</subject><subject>Patients</subject><subject>Plasma</subject><subject>Regression analysis</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Urokinase</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><recordid>eNptkt9rFDEQx4Motpx98l0WfBFka37uJk9ynFULhRZrfQ3ZZPbMuZtck90D_3tzttarmDxkSD7z_TKZQeglwaeMKfxuY0fCKGkYx0_QMcVtW2Mm2dOD-Aid5LzBZUnJKWmfoyOmBJG8Vcfo-mxnhtlMPoYq9tV1HOZugOomxR8-mAzV1WDy6ENcQ6iWdvI7M8VUfQEL233gQ7W6_Hb-oSaquioyEKb8Aj3rzZDh5P5coJuPZ19Xn-uLy0_nq-VFbRmVU930jelUK50irRMCgAGjvXBCtaA6aWwnpOAMXI-tpFQq6JwVjjgHrHOcswV6f6e7nbsRnC3eyQx6m_xo0k8djdePX4L_rtdxpwkRvOFKFIU39wop3s6QJz36bGEYTIA4Z80IlS3n-LfZ63_QTZxTKPXtqQZzRRX5S63NANqHPhZjuxfVS0kE40KVjizQ6X-osh2M3sYAvS_3jxLe3iXYFHNO0D8USbDez4E-mINCvzr8lwf2T9fZL95KrH4</recordid><startdate>20241023</startdate><enddate>20241023</enddate><creator>Arientová, Simona</creator><creator>Matúšková, Kateřina</creator><creator>Bartoš, Oldřich</creator><creator>Beran, Ondřej</creator><creator>Holub, Michal</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1894-2605</orcidid></search><sort><creationdate>20241023</creationdate><title>Evaluation of Soluble Urokinase Plasminogen Activator Receptor in COVID-19 Patients</title><author>Arientová, Simona ; Matúšková, Kateřina ; Bartoš, Oldřich ; Beran, Ondřej ; Holub, Michal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-6f6ab978d917d55ee3e32f5d597e9b8acb58543edf0c82289ebdc5d1dde3bd443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Analysis</topic><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Blood</topic><topic>Care and treatment</topic><topic>Comorbidity</topic><topic>COVID-19</topic><topic>Creatinine</topic><topic>Diagnosis</topic><topic>Disease</topic><topic>Dosage and administration</topic><topic>Hospital patients</topic><topic>Hospitalization</topic><topic>Hospitals</topic><topic>Infections</topic><topic>Laboratories</topic><topic>Mortality</topic><topic>Oxygen therapy</topic><topic>Pandemics</topic><topic>Patients</topic><topic>Plasma</topic><topic>Regression analysis</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Urokinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arientová, Simona</creatorcontrib><creatorcontrib>Matúšková, Kateřina</creatorcontrib><creatorcontrib>Bartoš, Oldřich</creatorcontrib><creatorcontrib>Beran, Ondřej</creatorcontrib><creatorcontrib>Holub, Michal</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arientová, Simona</au><au>Matúšková, Kateřina</au><au>Bartoš, Oldřich</au><au>Beran, Ondřej</au><au>Holub, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Soluble Urokinase Plasminogen Activator Receptor in COVID-19 Patients</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2024-10-23</date><risdate>2024</risdate><volume>13</volume><issue>21</issue><spage>6340</spage><pages>6340-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>This retrospective study analyzed soluble urokinase plasminogen activator receptor (suPAR) plasma levels alongside routine inflammatory markers, including the neutrophil-to-lymphocyte count ratio, C-reactive protein (CRP), interleukin-6 (IL-6), procalcitonin (PCT), and D-dimers in COVID-19 patients hospitalized during the Omicron wave of the pandemic.
We measured plasma suPAR levels using a suPARnostic
Quick Triage kit. We divided COVID-19 patients into two groups based on the severity of SARS-CoV-2 infection according to the National Institutes of Health (NIH) criteria. The logistic regression analysis tested the predictive value of the biomarkers.
We evaluated 160 consecutive COVID-19 patients hospitalized between January and August 2022. The cohort exhibited a high incidence of comorbidities, with an in-hospital mortality rate of 5.6%. Upon admission, the median suPAR plasma levels were not significantly different between patients with mild COVID-19 (n = 110) and those with moderate/severe disease (n = 50), with 7.25 ng/mL and 7.55 ng/mL, respectively. We observed significant differences (
< 0.01) between the groups for CRP and IL-6 levels that were higher in moderate/severe disease than in mild infection. Additionally, suPAR plasma levels were above the normal range (0-2.00 ng/mL) in all patients, with a significant positive correlation identified between suPAR levels and serum IL-6, PCT, and creatinine levels.
These findings indicate that COVID-19 during the Omicron wave is strongly associated with elevated suPAR levels; however, these levels do not directly correlate with the severity of SARS-CoV-2 infection.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39518479</pmid><doi>10.3390/jcm13216340</doi><orcidid>https://orcid.org/0000-0003-1894-2605</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Biological markers Biomarkers Blood Care and treatment Comorbidity COVID-19 Creatinine Diagnosis Disease Dosage and administration Hospital patients Hospitalization Hospitals Infections Laboratories Mortality Oxygen therapy Pandemics Patients Plasma Regression analysis Severe acute respiratory syndrome coronavirus 2 Urokinase |
title | Evaluation of Soluble Urokinase Plasminogen Activator Receptor in COVID-19 Patients |
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