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Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia
PURPOSE: To evaluate the role of C-reactive protein (CRP) in predicting severe COVID-19 patients. METHODS: A prospective observational cohort study was conducted from July 15 to October 28, 2020, at Kuyha COVID-19 isolation and treatment center hospital, Mekelle City, Northern Ethiopia. A total of 6...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199690/ https://www.ncbi.nlm.nih.gov/pubmed/37215303 http://dx.doi.org/10.2147/IDR.S410053 |
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author | Gebrecherkos, Teklay Challa, Feyissa Tasew, Geremew Gessesse, Zekarias Kiros, Yazezew Gebreegziabxier, Atsbeha Abdulkader, Mahmud Desta, Abraham Aregay Atsbaha, Ataklti Hailu Tollera, Getachew Abrahim, Saro Urban, Britta C Schallig, Henk Rinke de Wit, Tobias Wolday, Dawit |
author_facet | Gebrecherkos, Teklay Challa, Feyissa Tasew, Geremew Gessesse, Zekarias Kiros, Yazezew Gebreegziabxier, Atsbeha Abdulkader, Mahmud Desta, Abraham Aregay Atsbaha, Ataklti Hailu Tollera, Getachew Abrahim, Saro Urban, Britta C Schallig, Henk Rinke de Wit, Tobias Wolday, Dawit |
author_sort | Gebrecherkos, Teklay |
collection | PubMed |
description | PURPOSE: To evaluate the role of C-reactive protein (CRP) in predicting severe COVID-19 patients. METHODS: A prospective observational cohort study was conducted from July 15 to October 28, 2020, at Kuyha COVID-19 isolation and treatment center hospital, Mekelle City, Northern Ethiopia. A total of 670 blood samples were collected serially. SARS-CoV-2 infection was confirmed by RT-PCR from nasopharyngeal swabs and CRP concentration was determined using Cobas Integra 400 Plus (Roche). Data were analyzed using STATA version 14. P-value <0.05 was considered statistically significant. RESULTS: Overall, COVID-19 patients had significantly elevated CRP at baseline when compared to PCR-negative controls [median 11.1 (IQR: 2.0–127.8) mg/L vs 0.9 (IQR: 0.5–1.9) mg/L; p=0.0004)]. Those with severe COVID-19 clinical presentation had significantly higher median CRP levels compared to those with non-severe cases [166.1 (IQR: 48.6–332.5) mg/L vs 2.4 (IQR: 1.2–7.6) mg/L; p<0.00001)]. Moreover, COVID-19 patients exhibited higher median CRP levels at baseline [58 (IQR: 2.0–127.8) mg/L] that decreased significantly to 2.4 (IQR: 1.4–3.9) mg/L after 40 days after symptom onset (p<0.0001). Performance of CRP levels determined using ROC analysis distinguished severe from non-severe COVID-19 patients, with an AUC value of 0.83 (95% CI: 0.73–0.91; p=0.001; 77.4% sensitivity and 89.4% specificity). In multivariable analysis, CRP levels above 30 mg/L were significantly associated with an increased risk of developing severe COVID-19 for those who have higher ages and comorbidities (ARR 3.99, 95% CI: 1.35–11.82; p=0.013). CONCLUSION: CRP was found to be an independent determinant factor for severe COVID-19 patients. Therefore, CRP levels in COVID-19 patients in African settings may provide a simple, prompt, and inexpensive assessment of the severity status at baseline and monitoring of treatment outcomes. |
format | Online Article Text |
id | pubmed-10199690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-101996902023-05-21 Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia Gebrecherkos, Teklay Challa, Feyissa Tasew, Geremew Gessesse, Zekarias Kiros, Yazezew Gebreegziabxier, Atsbeha Abdulkader, Mahmud Desta, Abraham Aregay Atsbaha, Ataklti Hailu Tollera, Getachew Abrahim, Saro Urban, Britta C Schallig, Henk Rinke de Wit, Tobias Wolday, Dawit Infect Drug Resist Original Research PURPOSE: To evaluate the role of C-reactive protein (CRP) in predicting severe COVID-19 patients. METHODS: A prospective observational cohort study was conducted from July 15 to October 28, 2020, at Kuyha COVID-19 isolation and treatment center hospital, Mekelle City, Northern Ethiopia. A total of 670 blood samples were collected serially. SARS-CoV-2 infection was confirmed by RT-PCR from nasopharyngeal swabs and CRP concentration was determined using Cobas Integra 400 Plus (Roche). Data were analyzed using STATA version 14. P-value <0.05 was considered statistically significant. RESULTS: Overall, COVID-19 patients had significantly elevated CRP at baseline when compared to PCR-negative controls [median 11.1 (IQR: 2.0–127.8) mg/L vs 0.9 (IQR: 0.5–1.9) mg/L; p=0.0004)]. Those with severe COVID-19 clinical presentation had significantly higher median CRP levels compared to those with non-severe cases [166.1 (IQR: 48.6–332.5) mg/L vs 2.4 (IQR: 1.2–7.6) mg/L; p<0.00001)]. Moreover, COVID-19 patients exhibited higher median CRP levels at baseline [58 (IQR: 2.0–127.8) mg/L] that decreased significantly to 2.4 (IQR: 1.4–3.9) mg/L after 40 days after symptom onset (p<0.0001). Performance of CRP levels determined using ROC analysis distinguished severe from non-severe COVID-19 patients, with an AUC value of 0.83 (95% CI: 0.73–0.91; p=0.001; 77.4% sensitivity and 89.4% specificity). In multivariable analysis, CRP levels above 30 mg/L were significantly associated with an increased risk of developing severe COVID-19 for those who have higher ages and comorbidities (ARR 3.99, 95% CI: 1.35–11.82; p=0.013). CONCLUSION: CRP was found to be an independent determinant factor for severe COVID-19 patients. Therefore, CRP levels in COVID-19 patients in African settings may provide a simple, prompt, and inexpensive assessment of the severity status at baseline and monitoring of treatment outcomes. Dove 2023-05-16 /pmc/articles/PMC10199690/ /pubmed/37215303 http://dx.doi.org/10.2147/IDR.S410053 Text en © 2023 Gebrecherkos et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Gebrecherkos, Teklay Challa, Feyissa Tasew, Geremew Gessesse, Zekarias Kiros, Yazezew Gebreegziabxier, Atsbeha Abdulkader, Mahmud Desta, Abraham Aregay Atsbaha, Ataklti Hailu Tollera, Getachew Abrahim, Saro Urban, Britta C Schallig, Henk Rinke de Wit, Tobias Wolday, Dawit Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title | Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title_full | Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title_fullStr | Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title_full_unstemmed | Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title_short | Prognostic Value of C-Reactive Protein in SARS-CoV-2 Infection: A Simplified Biomarker of COVID-19 Severity in Northern Ethiopia |
title_sort | prognostic value of c-reactive protein in sars-cov-2 infection: a simplified biomarker of covid-19 severity in northern ethiopia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199690/ https://www.ncbi.nlm.nih.gov/pubmed/37215303 http://dx.doi.org/10.2147/IDR.S410053 |
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