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Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis
Background: The potential role of selenium in preventing chronic liver diseases remains controversial. This meta-analysis aimed to summarize the available evidence from observational studies and intervention trials that had evaluated the associations between body selenium status and chronic liver di...
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/PMC8912406/ https://www.ncbi.nlm.nih.gov/pubmed/35267927 http://dx.doi.org/10.3390/nu14050952 |
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author | Lin, Yaduan He, Fanchen Lian, Shaoyan Xie, Binbin Liu, Ting He, Jiang Liu, Chaoqun |
author_facet | Lin, Yaduan He, Fanchen Lian, Shaoyan Xie, Binbin Liu, Ting He, Jiang Liu, Chaoqun |
author_sort | Lin, Yaduan |
collection | PubMed |
description | Background: The potential role of selenium in preventing chronic liver diseases remains controversial. This meta-analysis aimed to summarize the available evidence from observational studies and intervention trials that had evaluated the associations between body selenium status and chronic liver diseases. Methods: We comprehensively searched MEDLINE, Embase, Web of Science, and Cochrane Library from inception to April 2021. The study protocol was registered at PROSPERO (CRD42020210144). Relative risks (RR) for the highest versus the lowest level of selenium and standard mean differences (SMD) with 95% confidence intervals (CI) were pooled using random-effects models. Heterogeneity and publication bias were evaluated using the I(2) statistic and Egger’s regression test, respectively. Results: There were 50 studies with 9875 cases and 12975 population controls in the final analysis. Patients with hepatitis (SMD = −1.78, 95% CI: −2.22 to −1.34), liver cirrhosis (SMD = −2.06, 95% CI: −2.48 to −1.63), and liver cancer (SMD = −2.71, 95% CI: −3.31 to −2.11) had significantly lower selenium levels than controls, whereas there was no significant difference in patients with fatty liver diseases (SMD = 1.06, 95% CI: −1.78 to 3.89). Moreover, the meta-analysis showed that a higher selenium level was significantly associated with a 41% decrease in the incidence of significant advanced chronic liver diseases (RR = 0.59, 95% CI: 0.49 to 0.72). Conclusion: Our meta-analysis suggested that both body selenium status and selenium intake were negatively associated with hepatitis, cirrhosis, and liver cancer. However, the associations for fatty liver diseases were conflicting and need to be established in prospective trials. |
format | Online Article Text |
id | pubmed-8912406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89124062022-03-11 Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis Lin, Yaduan He, Fanchen Lian, Shaoyan Xie, Binbin Liu, Ting He, Jiang Liu, Chaoqun Nutrients Review Background: The potential role of selenium in preventing chronic liver diseases remains controversial. This meta-analysis aimed to summarize the available evidence from observational studies and intervention trials that had evaluated the associations between body selenium status and chronic liver diseases. Methods: We comprehensively searched MEDLINE, Embase, Web of Science, and Cochrane Library from inception to April 2021. The study protocol was registered at PROSPERO (CRD42020210144). Relative risks (RR) for the highest versus the lowest level of selenium and standard mean differences (SMD) with 95% confidence intervals (CI) were pooled using random-effects models. Heterogeneity and publication bias were evaluated using the I(2) statistic and Egger’s regression test, respectively. Results: There were 50 studies with 9875 cases and 12975 population controls in the final analysis. Patients with hepatitis (SMD = −1.78, 95% CI: −2.22 to −1.34), liver cirrhosis (SMD = −2.06, 95% CI: −2.48 to −1.63), and liver cancer (SMD = −2.71, 95% CI: −3.31 to −2.11) had significantly lower selenium levels than controls, whereas there was no significant difference in patients with fatty liver diseases (SMD = 1.06, 95% CI: −1.78 to 3.89). Moreover, the meta-analysis showed that a higher selenium level was significantly associated with a 41% decrease in the incidence of significant advanced chronic liver diseases (RR = 0.59, 95% CI: 0.49 to 0.72). Conclusion: Our meta-analysis suggested that both body selenium status and selenium intake were negatively associated with hepatitis, cirrhosis, and liver cancer. However, the associations for fatty liver diseases were conflicting and need to be established in prospective trials. MDPI 2022-02-23 /pmc/articles/PMC8912406/ /pubmed/35267927 http://dx.doi.org/10.3390/nu14050952 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 | Review Lin, Yaduan He, Fanchen Lian, Shaoyan Xie, Binbin Liu, Ting He, Jiang Liu, Chaoqun Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title | Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title_full | Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title_fullStr | Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title_full_unstemmed | Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title_short | Selenium Status in Patients with Chronic Liver Disease: A Systematic Review and Meta-Analysis |
title_sort | selenium status in patients with chronic liver disease: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912406/ https://www.ncbi.nlm.nih.gov/pubmed/35267927 http://dx.doi.org/10.3390/nu14050952 |
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