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Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis

AIM: This study aimed to determine whether patients with elevated CRP, TNFα, and IL-6 levels may be at increased risk for severe infection and liver damage of COVID-19. BACKGROUND: The COVID-19 outbreak is a serious health problem to human beings. The evidence suggests that inflammatory markers rela...

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Autores principales: Amiri-Dashatan, Nasrin, Koushki, Mehdi, Ghorbani, Fatemeh, Naderi, Nosratollah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682967/
https://www.ncbi.nlm.nih.gov/pubmed/33244370
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author Amiri-Dashatan, Nasrin
Koushki, Mehdi
Ghorbani, Fatemeh
Naderi, Nosratollah
author_facet Amiri-Dashatan, Nasrin
Koushki, Mehdi
Ghorbani, Fatemeh
Naderi, Nosratollah
author_sort Amiri-Dashatan, Nasrin
collection PubMed
description AIM: This study aimed to determine whether patients with elevated CRP, TNFα, and IL-6 levels may be at increased risk for severe infection and liver damage of COVID-19. BACKGROUND: The COVID-19 outbreak is a serious health problem to human beings. The evidence suggests that inflammatory markers related to liver damage increase in severe forms of COVID-19 compared to mild cases. METHODS: The electronic databases ISI Web of Science, EMBASE, and Cochrane Library were comprehensively searched for articles published up to May, 2020. Data from each identified study was combined using the random effects model to estimate standardized mean difference (SMD) and 95% confidence intervals (95% CIs). Sensitivity and publication bias were also calculated. RESULTS: Totally, 23 studies were included in this meta-analysis comprising 4313 patients with COVID-19. The random effects results demonstrated that patients with severe COVID-19 had significantly higher levels of CRP [SMD = 3.26 mg/L; (95% CI 2.5, 3.9); p<0.05; I2 = 98.02%; PHeterogeneity = 0.00], TNFα [SMD = 1.78 ng/mL; (95% CI 0.39, 3.1); p=0.012; I2 = 98.2%; PHeterogeneity = 0.00], and IL-6 [ SMD = 3.67 ng/mL; (95% CI 2.4, 4.8); p<0.05; I2 = 97.8%; PHeterogeneity = 0.00] compared with those with the mild form of the disease. Significant heterogeneity was present. No significant publication bias was observed in the meta-analysis. Sensitivity analyses showed a similar effect size while reducing the heterogeneity. CONCLUSION: The data suggests that enhanced inflammation may be associated with COVID-19-related liver damage, possibly involving inflammatory marker-related mechanisms.
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spelling pubmed-76829672020-11-25 Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis Amiri-Dashatan, Nasrin Koushki, Mehdi Ghorbani, Fatemeh Naderi, Nosratollah Gastroenterol Hepatol Bed Bench Systematic Review AIM: This study aimed to determine whether patients with elevated CRP, TNFα, and IL-6 levels may be at increased risk for severe infection and liver damage of COVID-19. BACKGROUND: The COVID-19 outbreak is a serious health problem to human beings. The evidence suggests that inflammatory markers related to liver damage increase in severe forms of COVID-19 compared to mild cases. METHODS: The electronic databases ISI Web of Science, EMBASE, and Cochrane Library were comprehensively searched for articles published up to May, 2020. Data from each identified study was combined using the random effects model to estimate standardized mean difference (SMD) and 95% confidence intervals (95% CIs). Sensitivity and publication bias were also calculated. RESULTS: Totally, 23 studies were included in this meta-analysis comprising 4313 patients with COVID-19. The random effects results demonstrated that patients with severe COVID-19 had significantly higher levels of CRP [SMD = 3.26 mg/L; (95% CI 2.5, 3.9); p<0.05; I2 = 98.02%; PHeterogeneity = 0.00], TNFα [SMD = 1.78 ng/mL; (95% CI 0.39, 3.1); p=0.012; I2 = 98.2%; PHeterogeneity = 0.00], and IL-6 [ SMD = 3.67 ng/mL; (95% CI 2.4, 4.8); p<0.05; I2 = 97.8%; PHeterogeneity = 0.00] compared with those with the mild form of the disease. Significant heterogeneity was present. No significant publication bias was observed in the meta-analysis. Sensitivity analyses showed a similar effect size while reducing the heterogeneity. CONCLUSION: The data suggests that enhanced inflammation may be associated with COVID-19-related liver damage, possibly involving inflammatory marker-related mechanisms. Shaheed Beheshti University of Medical Sciences 2020 /pmc/articles/PMC7682967/ /pubmed/33244370 Text en ©2020 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Systematic Review
Amiri-Dashatan, Nasrin
Koushki, Mehdi
Ghorbani, Fatemeh
Naderi, Nosratollah
Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title_full Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title_fullStr Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title_full_unstemmed Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title_short Increased inflammatory markers correlate with liver damage and predict severe COVID-19: a systematic review and meta-analysis
title_sort increased inflammatory markers correlate with liver damage and predict severe covid-19: a systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682967/
https://www.ncbi.nlm.nih.gov/pubmed/33244370
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