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The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis

Although several studies have shown that each of the metabolic syndrome (MetS) components can be a risk factor for erosive esophagitis (EE), the association between MetS and EE is still a challenging subject, as studies about this association have shown inconsistent results. Therefore, this study wa...

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Autores principales: Azami, Milad, Salamati, Majid, Ranjbar, Reza, Sahebkar, Amirhossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8678055/
https://www.ncbi.nlm.nih.gov/pubmed/34924903
http://dx.doi.org/10.17179/excli2021-4282
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author Azami, Milad
Salamati, Majid
Ranjbar, Reza
Sahebkar, Amirhossein
author_facet Azami, Milad
Salamati, Majid
Ranjbar, Reza
Sahebkar, Amirhossein
author_sort Azami, Milad
collection PubMed
description Although several studies have shown that each of the metabolic syndrome (MetS) components can be a risk factor for erosive esophagitis (EE), the association between MetS and EE is still a challenging subject, as studies about this association have shown inconsistent results. Therefore, this study was conducted to evaluate the association between MetS and EE. In this study, we followed the MOOSE protocol and the PRISMA guidelines for reporting the results. Web of Science (ISI), Cochrane Library (Cochrane Database of Systematic Reviews - CDSR), EMBASE, Scopus, Science Direct, PubMed/Medline, EBSCO, CINAHL, and Google Scholar search engine were searched for articles published until January 2021. Heterogeneity between studies was estimated by I2 index and Q test. All analyses were performed using Comprehensive Meta-Analysis Software. Finally, 12 studies entered the meta-analysis process after qualitative assessment. MetS was significantly associated with increased risk of EE (OR=1.488 [95 % CI: 1.352-1.638], P<0.001; Heterogeneity: I2= 55.57, P<0.001) in 12 studies with a sample size of 45285 (12825 cases and 29377 controls). In subgroup analysis based on types of studies (P=0.832), MetS diagnostic criteria (P=0.083) and quality of studies (P=0.612), no significant association was found. Sensitivity analysis showed that the overall estimation of effect size is still robust after omission of individual studies from the meta-analysis. Publication bias based on the Begg's test (P=0.945) and Egger's test (P=0.753) were not significant. MetS increases the risk of EE compared to control groups. Future studies should examine if MetS treatment reduces the risk of EE.
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spelling pubmed-86780552021-12-17 The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis Azami, Milad Salamati, Majid Ranjbar, Reza Sahebkar, Amirhossein EXCLI J Review Article Although several studies have shown that each of the metabolic syndrome (MetS) components can be a risk factor for erosive esophagitis (EE), the association between MetS and EE is still a challenging subject, as studies about this association have shown inconsistent results. Therefore, this study was conducted to evaluate the association between MetS and EE. In this study, we followed the MOOSE protocol and the PRISMA guidelines for reporting the results. Web of Science (ISI), Cochrane Library (Cochrane Database of Systematic Reviews - CDSR), EMBASE, Scopus, Science Direct, PubMed/Medline, EBSCO, CINAHL, and Google Scholar search engine were searched for articles published until January 2021. Heterogeneity between studies was estimated by I2 index and Q test. All analyses were performed using Comprehensive Meta-Analysis Software. Finally, 12 studies entered the meta-analysis process after qualitative assessment. MetS was significantly associated with increased risk of EE (OR=1.488 [95 % CI: 1.352-1.638], P<0.001; Heterogeneity: I2= 55.57, P<0.001) in 12 studies with a sample size of 45285 (12825 cases and 29377 controls). In subgroup analysis based on types of studies (P=0.832), MetS diagnostic criteria (P=0.083) and quality of studies (P=0.612), no significant association was found. Sensitivity analysis showed that the overall estimation of effect size is still robust after omission of individual studies from the meta-analysis. Publication bias based on the Begg's test (P=0.945) and Egger's test (P=0.753) were not significant. MetS increases the risk of EE compared to control groups. Future studies should examine if MetS treatment reduces the risk of EE. Leibniz Research Centre for Working Environment and Human Factors 2021-11-08 /pmc/articles/PMC8678055/ /pubmed/34924903 http://dx.doi.org/10.17179/excli2021-4282 Text en Copyright © 2021 Azami et al. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Review Article
Azami, Milad
Salamati, Majid
Ranjbar, Reza
Sahebkar, Amirhossein
The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title_full The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title_fullStr The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title_full_unstemmed The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title_short The association between metabolic syndrome and erosive esophagitis: A systematic review and meta-analysis
title_sort association between metabolic syndrome and erosive esophagitis: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8678055/
https://www.ncbi.nlm.nih.gov/pubmed/34924903
http://dx.doi.org/10.17179/excli2021-4282
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