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Free Zinc as a Predictive Marker for COVID-19 Mortality Risk
Free zinc is considered to be the exchangeable and biological active form of zinc in serum, and is discussed to be a suitable biomarker for alterations in body zinc homeostasis and related diseases. Given that coronavirus disease 2019 (COVID-19) is characterized by a marked decrease in total serum z...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9002649/ https://www.ncbi.nlm.nih.gov/pubmed/35406020 http://dx.doi.org/10.3390/nu14071407 |
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author | Maares, Maria Hackler, Julian Haupt, Alessia Heller, Raban Arved Bachmann, Manuel Diegmann, Joachim Moghaddam, Arash Schomburg, Lutz Haase, Hajo |
author_facet | Maares, Maria Hackler, Julian Haupt, Alessia Heller, Raban Arved Bachmann, Manuel Diegmann, Joachim Moghaddam, Arash Schomburg, Lutz Haase, Hajo |
author_sort | Maares, Maria |
collection | PubMed |
description | Free zinc is considered to be the exchangeable and biological active form of zinc in serum, and is discussed to be a suitable biomarker for alterations in body zinc homeostasis and related diseases. Given that coronavirus disease 2019 (COVID-19) is characterized by a marked decrease in total serum zinc, and clinical data indicate that zinc status impacts the susceptibility and severity of the infection, we hypothesized that free zinc in serum might be altered in response to SARS-CoV-2 infection and may reflect disease severity. To test this hypothesis, free zinc concentrations in serum samples of survivors and nonsurvivors of COVID-19 were analyzed by fluorometric microassay. Similar to the reported total serum zinc deficit measured by total reflection X-ray fluorescence, free serum zinc in COVID-19 patients was considerably lower than that in control subjects, and surviving patients displayed significantly higher levels of free zinc than those of nonsurvivors (mean ± SD; 0.4 ± 0.2 nM vs. 0.2 ± 0.1 nM; p = 0.0004). In contrast to recovering total zinc concentrations (r = 0.706, p < 0.001) or the declining copper–zinc ratio (r = −0.646; p < 0.001), free zinc concentrations remained unaltered with time in COVID-19 nonsurvivors. Free serum zinc concentrations were particularly low in male as compared to female patients (mean ± SD; 0.4 ± 0.2 nM vs. 0.2 ± 0.1 nM; p = 0.0003). This is of particular interest, as the male sex is described as a risk factor for severe COVID-19. Overall, results indicate that depressed free serum zinc levels are associated with increased risk of death in COVID-19, suggesting that free zinc may serve as a novel prognostic marker for the severity and course of COVID-19. |
format | Online Article Text |
id | pubmed-9002649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90026492022-04-13 Free Zinc as a Predictive Marker for COVID-19 Mortality Risk Maares, Maria Hackler, Julian Haupt, Alessia Heller, Raban Arved Bachmann, Manuel Diegmann, Joachim Moghaddam, Arash Schomburg, Lutz Haase, Hajo Nutrients Article Free zinc is considered to be the exchangeable and biological active form of zinc in serum, and is discussed to be a suitable biomarker for alterations in body zinc homeostasis and related diseases. Given that coronavirus disease 2019 (COVID-19) is characterized by a marked decrease in total serum zinc, and clinical data indicate that zinc status impacts the susceptibility and severity of the infection, we hypothesized that free zinc in serum might be altered in response to SARS-CoV-2 infection and may reflect disease severity. To test this hypothesis, free zinc concentrations in serum samples of survivors and nonsurvivors of COVID-19 were analyzed by fluorometric microassay. Similar to the reported total serum zinc deficit measured by total reflection X-ray fluorescence, free serum zinc in COVID-19 patients was considerably lower than that in control subjects, and surviving patients displayed significantly higher levels of free zinc than those of nonsurvivors (mean ± SD; 0.4 ± 0.2 nM vs. 0.2 ± 0.1 nM; p = 0.0004). In contrast to recovering total zinc concentrations (r = 0.706, p < 0.001) or the declining copper–zinc ratio (r = −0.646; p < 0.001), free zinc concentrations remained unaltered with time in COVID-19 nonsurvivors. Free serum zinc concentrations were particularly low in male as compared to female patients (mean ± SD; 0.4 ± 0.2 nM vs. 0.2 ± 0.1 nM; p = 0.0003). This is of particular interest, as the male sex is described as a risk factor for severe COVID-19. Overall, results indicate that depressed free serum zinc levels are associated with increased risk of death in COVID-19, suggesting that free zinc may serve as a novel prognostic marker for the severity and course of COVID-19. MDPI 2022-03-28 /pmc/articles/PMC9002649/ /pubmed/35406020 http://dx.doi.org/10.3390/nu14071407 Text en © 2022 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 Maares, Maria Hackler, Julian Haupt, Alessia Heller, Raban Arved Bachmann, Manuel Diegmann, Joachim Moghaddam, Arash Schomburg, Lutz Haase, Hajo Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title | Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title_full | Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title_fullStr | Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title_full_unstemmed | Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title_short | Free Zinc as a Predictive Marker for COVID-19 Mortality Risk |
title_sort | free zinc as a predictive marker for covid-19 mortality risk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9002649/ https://www.ncbi.nlm.nih.gov/pubmed/35406020 http://dx.doi.org/10.3390/nu14071407 |
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