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Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis
BACKGROUND: Barrett esophagus (BE) is considered precursor condition of esophageal adenocarcinoma. Its incidence and prevalence are increasing in general population. Studies reported that metabolic syndrome (MS) or diabetes mellitus (DM) is related to increased risk of BE. Current study was to asses...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979793/ https://www.ncbi.nlm.nih.gov/pubmed/27495039 http://dx.doi.org/10.1097/MD.0000000000004338 |
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author | He, Qiong Li, Jian-dong Huang, Wei Zhu, Wen-chang Yang, Jian-quan |
author_facet | He, Qiong Li, Jian-dong Huang, Wei Zhu, Wen-chang Yang, Jian-quan |
author_sort | He, Qiong |
collection | PubMed |
description | BACKGROUND: Barrett esophagus (BE) is considered precursor condition of esophageal adenocarcinoma. Its incidence and prevalence are increasing in general population. Studies reported that metabolic syndrome (MS) or diabetes mellitus (DM) is related to increased risk of BE. Current study was to assess and better understand the relationship between MS /DM and BE. METHODS: Electronic search was conducted in the database Pubmed/Medline (-December, 2015), Embase (-December, 2015), Cochrane Library (-December, 2015), and Web of Knowledge (-December, 2015). Studies included were assessed with summary odds ratios (ORs) with 95% confidence intervals (CIs) and compared exposure group with control group. The heterogeneity was examined by the funnel plot and the Egger's test. Subgroup analyses and sensitive analyses were performed for the detection of possible heterogeneity and impact on stability of analysis results. RESULTS: Twelve publications met the criteria and included 355,311 subjects were analyzed. The pooled results showed MS was closely associated with increased risk of BE (OR = 1.23; 95%CI 1.03–1.47; P = 0.024), and yet DM did not significantly increase the risk of BE (OR = 1.07; 95%CI 0.82–1.38; P = 0.627). Substantial heterogeneities were detected. No significant publication bias was detected by Egger's test (P = 0.23). CONCLUSIONS: Based on the results of current meta-analysis, MS is associated with increased risk of BE. Further long-term follow-up prospective study needs to verify the current results, and definite pathophysiological mechanism needs to be further investigated and clearly elucidated. |
format | Online Article Text |
id | pubmed-4979793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49797932016-08-18 Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis He, Qiong Li, Jian-dong Huang, Wei Zhu, Wen-chang Yang, Jian-quan Medicine (Baltimore) 4500 BACKGROUND: Barrett esophagus (BE) is considered precursor condition of esophageal adenocarcinoma. Its incidence and prevalence are increasing in general population. Studies reported that metabolic syndrome (MS) or diabetes mellitus (DM) is related to increased risk of BE. Current study was to assess and better understand the relationship between MS /DM and BE. METHODS: Electronic search was conducted in the database Pubmed/Medline (-December, 2015), Embase (-December, 2015), Cochrane Library (-December, 2015), and Web of Knowledge (-December, 2015). Studies included were assessed with summary odds ratios (ORs) with 95% confidence intervals (CIs) and compared exposure group with control group. The heterogeneity was examined by the funnel plot and the Egger's test. Subgroup analyses and sensitive analyses were performed for the detection of possible heterogeneity and impact on stability of analysis results. RESULTS: Twelve publications met the criteria and included 355,311 subjects were analyzed. The pooled results showed MS was closely associated with increased risk of BE (OR = 1.23; 95%CI 1.03–1.47; P = 0.024), and yet DM did not significantly increase the risk of BE (OR = 1.07; 95%CI 0.82–1.38; P = 0.627). Substantial heterogeneities were detected. No significant publication bias was detected by Egger's test (P = 0.23). CONCLUSIONS: Based on the results of current meta-analysis, MS is associated with increased risk of BE. Further long-term follow-up prospective study needs to verify the current results, and definite pathophysiological mechanism needs to be further investigated and clearly elucidated. Wolters Kluwer Health 2016-08-07 /pmc/articles/PMC4979793/ /pubmed/27495039 http://dx.doi.org/10.1097/MD.0000000000004338 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 4500 He, Qiong Li, Jian-dong Huang, Wei Zhu, Wen-chang Yang, Jian-quan Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title | Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title_full | Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title_fullStr | Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title_full_unstemmed | Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title_short | Metabolic syndrome is associated with increased risk of Barrett esophagus: A meta-analysis |
title_sort | metabolic syndrome is associated with increased risk of barrett esophagus: a meta-analysis |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979793/ https://www.ncbi.nlm.nih.gov/pubmed/27495039 http://dx.doi.org/10.1097/MD.0000000000004338 |
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