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Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients

Background: The Coronavirus Disease-19 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has been declared a worldwide pandemic. The severity of COVID-19 varies greatly across infected individuals. Possible factors may include plasma levels of 25(OH)D and vitamin...

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Autores principales: Alabdullatif, Wajude, Almnaizel, Ahmad, Alhijji, Ali, Alshathri, Aldanah, Albarrag, Ahmed, Bindayel, Iman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142640/
https://www.ncbi.nlm.nih.gov/pubmed/37111039
http://dx.doi.org/10.3390/nu15081818
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author Alabdullatif, Wajude
Almnaizel, Ahmad
Alhijji, Ali
Alshathri, Aldanah
Albarrag, Ahmed
Bindayel, Iman
author_facet Alabdullatif, Wajude
Almnaizel, Ahmad
Alhijji, Ali
Alshathri, Aldanah
Albarrag, Ahmed
Bindayel, Iman
author_sort Alabdullatif, Wajude
collection PubMed
description Background: The Coronavirus Disease-19 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has been declared a worldwide pandemic. The severity of COVID-19 varies greatly across infected individuals. Possible factors may include plasma levels of 25(OH)D and vitamin D binding protein (DBP), as both are involved in the host immune response. Other possible nutrition-related factors include malnutrition and/or obesity which disrupt the optimal host immune response to infections. Current literature shows inconsistent evidence about the association of plasma 25(OH)D(3) and DBP on infection severity and clinical outcomes. Objectives: This study aimed to measure plasma 25(OH)D(3) and DBP in hospitalized COVID-19 cases and assess their correlation with infection severity, inflammatory markers, and clinical outcome. Methods: 167 patients were included in this analytical cross-sectional study, of which 81 were critical and 86 were non-critical hospitalized COVID-19 patients. Plasma levels of 25(OH)D(3), DBP, and the inflammatory cytokines, IL-6, IL-8, IL-10, and TNF-α were assessed using the Enzyme-linked Immunosorbent Assay (ELISA). Information regarding biochemical and anthropometrical indices, hospital length of stay (LoS), and illness outcome was obtained from the medical records. Results: Plasma 25(OH)D(3) level was found to be significantly lower in critical compared to non-critical patients (Median = 8.38 (IQR = 2.33) vs. 9.83 (IQR = 3.03) nmol/L, respectively; p < 0.001), and it positively correlated with hospital LoS. However, plasma 25(OH)D(3) did not correlate with mortality or any of the inflammatory markers. DBP on the other hand correlated positively with mortality (r(s) = 0.188, p = 0.015) and hospital LoS (r(s) = 0.233, p = 0.002). DBP was significantly higher in critical than non-critical patients (Median = 1262.18 (IQR = 463.66) vs. 1153.35 (IQR = 418.46) ng/mL, respectively; p < 0.001). Furthermore, IL-6 and IL-8 were significantly higher in critical than non-critical patients. However, no differences were found in IL-10, TNF-α, IL-10/TNF-α, TNF-α/IL-10, IL-6/IL-10, or CRP between groups. Conclusion: The current study found that critical COVID-19 patients had lower 25(OH)D(3) than non-critical patients, yet, levels were found to be suboptimal in both groups. Further, critical patients had higher DBP levels as compared to non-critical patients. This finding may encourage future research to unravel the effects of this understudied protein that appears to have significant associations with inflammation, even though the precise mechanism is unknown.
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spelling pubmed-101426402023-04-29 Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients Alabdullatif, Wajude Almnaizel, Ahmad Alhijji, Ali Alshathri, Aldanah Albarrag, Ahmed Bindayel, Iman Nutrients Article Background: The Coronavirus Disease-19 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has been declared a worldwide pandemic. The severity of COVID-19 varies greatly across infected individuals. Possible factors may include plasma levels of 25(OH)D and vitamin D binding protein (DBP), as both are involved in the host immune response. Other possible nutrition-related factors include malnutrition and/or obesity which disrupt the optimal host immune response to infections. Current literature shows inconsistent evidence about the association of plasma 25(OH)D(3) and DBP on infection severity and clinical outcomes. Objectives: This study aimed to measure plasma 25(OH)D(3) and DBP in hospitalized COVID-19 cases and assess their correlation with infection severity, inflammatory markers, and clinical outcome. Methods: 167 patients were included in this analytical cross-sectional study, of which 81 were critical and 86 were non-critical hospitalized COVID-19 patients. Plasma levels of 25(OH)D(3), DBP, and the inflammatory cytokines, IL-6, IL-8, IL-10, and TNF-α were assessed using the Enzyme-linked Immunosorbent Assay (ELISA). Information regarding biochemical and anthropometrical indices, hospital length of stay (LoS), and illness outcome was obtained from the medical records. Results: Plasma 25(OH)D(3) level was found to be significantly lower in critical compared to non-critical patients (Median = 8.38 (IQR = 2.33) vs. 9.83 (IQR = 3.03) nmol/L, respectively; p < 0.001), and it positively correlated with hospital LoS. However, plasma 25(OH)D(3) did not correlate with mortality or any of the inflammatory markers. DBP on the other hand correlated positively with mortality (r(s) = 0.188, p = 0.015) and hospital LoS (r(s) = 0.233, p = 0.002). DBP was significantly higher in critical than non-critical patients (Median = 1262.18 (IQR = 463.66) vs. 1153.35 (IQR = 418.46) ng/mL, respectively; p < 0.001). Furthermore, IL-6 and IL-8 were significantly higher in critical than non-critical patients. However, no differences were found in IL-10, TNF-α, IL-10/TNF-α, TNF-α/IL-10, IL-6/IL-10, or CRP between groups. Conclusion: The current study found that critical COVID-19 patients had lower 25(OH)D(3) than non-critical patients, yet, levels were found to be suboptimal in both groups. Further, critical patients had higher DBP levels as compared to non-critical patients. This finding may encourage future research to unravel the effects of this understudied protein that appears to have significant associations with inflammation, even though the precise mechanism is unknown. MDPI 2023-04-10 /pmc/articles/PMC10142640/ /pubmed/37111039 http://dx.doi.org/10.3390/nu15081818 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Alabdullatif, Wajude
Almnaizel, Ahmad
Alhijji, Ali
Alshathri, Aldanah
Albarrag, Ahmed
Bindayel, Iman
Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title_full Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title_fullStr Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title_full_unstemmed Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title_short Correlation of Plasma 25(OH)D(3) and Vitamin D Binding Protein Levels with COVID-19 Severity and Outcome in Hospitalized Patients
title_sort correlation of plasma 25(oh)d(3) and vitamin d binding protein levels with covid-19 severity and outcome in hospitalized patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142640/
https://www.ncbi.nlm.nih.gov/pubmed/37111039
http://dx.doi.org/10.3390/nu15081818
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