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The association between different predictive biomarkers and mortality of COVID-19
BACKGROUND: Immunocompromised individuals are expected to be more prone to severe diseases and, subsequently, death. Genetic disorders and polymorphisms in genes involved in the immune system, such as human leukocyte antigen (HLA), inflammatory cytokines, and killer-cell immunoglobulin-like receptor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152825/ https://www.ncbi.nlm.nih.gov/pubmed/35669157 http://dx.doi.org/10.1186/s42269-022-00844-7 |
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author | Ansari, Narges Jahangiri, Mina Shirbandi, Kimia Ebrahimi, Mina Rahim, Fakher |
author_facet | Ansari, Narges Jahangiri, Mina Shirbandi, Kimia Ebrahimi, Mina Rahim, Fakher |
author_sort | Ansari, Narges |
collection | PubMed |
description | BACKGROUND: Immunocompromised individuals are expected to be more prone to severe diseases and, subsequently, death. Genetic disorders and polymorphisms in genes involved in the immune system, such as human leukocyte antigen (HLA), inflammatory cytokines, and killer-cell immunoglobulin-like receptors, can be involved in the immune system's response to various pathogens. In the current survey, the data were received from the world health organization, collected around the world. RESULTS: Spearman's coefficient correlation test for evaluating the relationship between the Daily Death Rates (DDR) and immunological variables showed a statistically significant correlation between the DDR and all immunological variables except TNFa857T, TNFa863A IL2330G, and IL2166T (P < 0.001). Also, there was a statistically significant correlation between the DDR and some HLA markers. CONCLUSION: This meta-analysis study shows that predictive biomarkers and mortality of COVID-19 are associated with HLA markers. However, these results should be confirmed in a more structured agreement. It is worth noting that the design of new studies should consider potential diseases with poor prognoses because they are related to these immune genetic markers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42269-022-00844-7. |
format | Online Article Text |
id | pubmed-9152825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91528252022-06-02 The association between different predictive biomarkers and mortality of COVID-19 Ansari, Narges Jahangiri, Mina Shirbandi, Kimia Ebrahimi, Mina Rahim, Fakher Bull Natl Res Cent Research BACKGROUND: Immunocompromised individuals are expected to be more prone to severe diseases and, subsequently, death. Genetic disorders and polymorphisms in genes involved in the immune system, such as human leukocyte antigen (HLA), inflammatory cytokines, and killer-cell immunoglobulin-like receptors, can be involved in the immune system's response to various pathogens. In the current survey, the data were received from the world health organization, collected around the world. RESULTS: Spearman's coefficient correlation test for evaluating the relationship between the Daily Death Rates (DDR) and immunological variables showed a statistically significant correlation between the DDR and all immunological variables except TNFa857T, TNFa863A IL2330G, and IL2166T (P < 0.001). Also, there was a statistically significant correlation between the DDR and some HLA markers. CONCLUSION: This meta-analysis study shows that predictive biomarkers and mortality of COVID-19 are associated with HLA markers. However, these results should be confirmed in a more structured agreement. It is worth noting that the design of new studies should consider potential diseases with poor prognoses because they are related to these immune genetic markers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42269-022-00844-7. Springer Berlin Heidelberg 2022-05-31 2022 /pmc/articles/PMC9152825/ /pubmed/35669157 http://dx.doi.org/10.1186/s42269-022-00844-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Ansari, Narges Jahangiri, Mina Shirbandi, Kimia Ebrahimi, Mina Rahim, Fakher The association between different predictive biomarkers and mortality of COVID-19 |
title | The association between different predictive biomarkers and mortality of COVID-19 |
title_full | The association between different predictive biomarkers and mortality of COVID-19 |
title_fullStr | The association between different predictive biomarkers and mortality of COVID-19 |
title_full_unstemmed | The association between different predictive biomarkers and mortality of COVID-19 |
title_short | The association between different predictive biomarkers and mortality of COVID-19 |
title_sort | association between different predictive biomarkers and mortality of covid-19 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152825/ https://www.ncbi.nlm.nih.gov/pubmed/35669157 http://dx.doi.org/10.1186/s42269-022-00844-7 |
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