COVID-19: Poor outcomes in patients with zinc deficiency
•Patients with coronavirus disease 2019 (COVID-19) had significantly low zinc levels in comparison to healthy controls.•Zinc deficient patients developed more complications (70.4% vs 30.0%, p = 0.009).•Zinc deficient COVID-19 patients had a prolonged hospital stay (7.9 vs 5.7 days, p = 0.048).•In vi...
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Published in | International journal of infectious diseases Vol. 100; pp. 343 - 349 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Canada
Elsevier Ltd
01.11.2020
Published by Elsevier Ltd on behalf of International Society for Infectious Diseases Elsevier |
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Abstract | •Patients with coronavirus disease 2019 (COVID-19) had significantly low zinc levels in comparison to healthy controls.•Zinc deficient patients developed more complications (70.4% vs 30.0%, p = 0.009).•Zinc deficient COVID-19 patients had a prolonged hospital stay (7.9 vs 5.7 days, p = 0.048).•In vitro studies have shown that reduced zinc levels favour the interaction of angiotensin-converting enzyme 2 (ACE2) with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein and likewise that increased zinc levels inhibit ACE2 expression resulting in reduced viral interaction.
Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity.
This was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels.
COVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4–94.6) μg/dl vs 105.8 (interquartile range 95.65–120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients.
The study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality. |
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AbstractList | Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity.
This was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels.
COVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4-94.6) μg/dl vs 105.8 (interquartile range 95.65-120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients.
The study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality. •Patients with coronavirus disease 2019 (COVID-19) had significantly low zinc levels in comparison to healthy controls.•Zinc deficient patients developed more complications (70.4% vs 30.0%, p = 0.009).•Zinc deficient COVID-19 patients had a prolonged hospital stay (7.9 vs 5.7 days, p = 0.048).•In vitro studies have shown that reduced zinc levels favour the interaction of angiotensin-converting enzyme 2 (ACE2) with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein and likewise that increased zinc levels inhibit ACE2 expression resulting in reduced viral interaction. Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity. This was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels. COVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4–94.6) μg/dl vs 105.8 (interquartile range 95.65–120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients. The study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality. Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity.BACKGROUNDZinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity.This was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels.METHODSThis was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels.COVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4-94.6) μg/dl vs 105.8 (interquartile range 95.65-120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients.RESULTSCOVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4-94.6) μg/dl vs 105.8 (interquartile range 95.65-120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients.The study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality.CONCLUSIONSThe study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality. Background: Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19). However, we do not know the clinical significance of serum Zinc levels in COVID-19 patients. The aim of this study was to determine the clinical significance of serum zinc in COVID-19 patients and to establish a correlation with disease severity. Methods: This was a prospective study of fasting zinc levels in COVID-19 patients at the time of hospitalization. An initial comparative analysis was conducted between COVID-19 patients and healthy controls. COVID-19 patients with zinc deficiency were compared to those with normal zinc levels. Results: COVID-19 patients (n = 47) showed significantly lower zinc levels when compared to healthy controls (n = 45): median 74.5 (interquartile range 53.4–94.6) μg/dl vs 105.8 (interquartile range 95.65–120.90) μg/dl (p < 0.001). Amongst the COVID-19 patients, 27 (57.4%) were found to be zinc deficient. These patients were found to have higher rates of complications (p = 0.009), acute respiratory distress syndrome (18.5% vs 0%, p = 0.06), corticosteroid therapy (p = 0.02), prolonged hospital stay (p = 0.05), and increased mortality (18.5% vs 0%, p = 0.06). The odds ratio (OR) of developing complications was 5.54 for zinc deficient COVID-19 patients. Conclusions: The study data clearly show that a significant number of COVID-19 patients were zinc deficient. These zinc deficient patients developed more complications, and the deficiency was associated with a prolonged hospital stay and increased mortality. |
Author | Ramani, Vidyalakshmi Rela, Mohamed Ramachandran, Hemalatha Danielraj, Silas Sekar, Padmini Nallathambi, Balaji Kaliamoorthy, Ilankumaran Manoharan, Shruthi Jothimani, Dinesh Kailasam, Ezhilarasan Narasimhan, Gomathy |
Author_xml | – sequence: 1 givenname: Dinesh orcidid: 0000-0003-4189-690X surname: Jothimani fullname: Jothimani, Dinesh email: dinesh.jothimani@relainstitute.com organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 2 givenname: Ezhilarasan surname: Kailasam fullname: Kailasam, Ezhilarasan organization: Department of Clinical Chemistry, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 3 givenname: Silas orcidid: 0000-0001-6468-5641 surname: Danielraj fullname: Danielraj, Silas organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 4 givenname: Balaji surname: Nallathambi fullname: Nallathambi, Balaji organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 5 givenname: Hemalatha surname: Ramachandran fullname: Ramachandran, Hemalatha organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 6 givenname: Padmini surname: Sekar fullname: Sekar, Padmini organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 7 givenname: Shruthi surname: Manoharan fullname: Manoharan, Shruthi organization: Department of Infectious Diseases, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 8 givenname: Vidyalakshmi surname: Ramani fullname: Ramani, Vidyalakshmi organization: Department of Infectious Diseases, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 9 givenname: Gomathy surname: Narasimhan fullname: Narasimhan, Gomathy organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 10 givenname: Ilankumaran surname: Kaliamoorthy fullname: Kaliamoorthy, Ilankumaran organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India – sequence: 11 givenname: Mohamed surname: Rela fullname: Rela, Mohamed organization: Institute of Liver Disease and Transplantation, Dr. Rela Institute and Medical Centre, Bharath Institute of Higher Education and Research, Chennai, India |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32920234$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2020 Copyright © 2020. Published by Elsevier Ltd. 2020 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2020 |
Copyright_xml | – notice: 2020 – notice: Copyright © 2020. Published by Elsevier Ltd. – notice: 2020 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2020 |
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the immune system and reducing inflammation and oxidative stress through diet and nutrition: considerations during the COVID-19 crisis publication-title: Nutrients doi: 10.3390/nu12061562 – volume: 46 start-page: 17 issue: 1 year: 2020 ident: 10.1016/j.ijid.2020.09.014_bib0120 article-title: Zinc and respiratory tract infections: perspectives for COVID-19 (Review) publication-title: Int J Mol Med |
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Snippet | •Patients with coronavirus disease 2019 (COVID-19) had significantly low zinc levels in comparison to healthy controls.•Zinc deficient patients developed more... Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019 (COVID-19).... Background: Zinc is a trace element with potent immunoregulatory and antiviral properties, and is utilized in the treatment of coronavirus disease 2019... |
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SubjectTerms | Adolescent Adult Aged Antiviral Agents - therapeutic use COVID-19 COVID-19 - blood COVID-19 - complications COVID-19 - therapy Female Hospitalization Humans Length of Stay Male Middle Aged Odds Ratio Pandemics Prospective Studies SARS-CoV-2 Treatment Outcome Young Adult Zinc Zinc - blood Zinc - deficiency |
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Title | COVID-19: Poor outcomes in patients with zinc deficiency |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S120197122030730X https://dx.doi.org/10.1016/j.ijid.2020.09.014 https://www.ncbi.nlm.nih.gov/pubmed/32920234 https://www.proquest.com/docview/2442600977 https://pubmed.ncbi.nlm.nih.gov/PMC7482607 https://doaj.org/article/2150730e57ed48a6a3edb40fefc40351 |
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