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Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis
BACKGROUND: Several studies have been performed to investigate the associations between interleukin (IL)-8 rs4073 polymorphism and acute pancreatitis (AP), but the results are inconclusive. We conducted this cumulative meta-analysis for a precise estimate of the relationship between IL-8 rs4073 poly...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657145/ https://www.ncbi.nlm.nih.gov/pubmed/31340771 http://dx.doi.org/10.1186/s12881-019-0861-4 |
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author | Li, Yening Bai, Jing He, Bing Wang, Nan Wang, Haoran Liu, Dongliang |
author_facet | Li, Yening Bai, Jing He, Bing Wang, Nan Wang, Haoran Liu, Dongliang |
author_sort | Li, Yening |
collection | PubMed |
description | BACKGROUND: Several studies have been performed to investigate the associations between interleukin (IL)-8 rs4073 polymorphism and acute pancreatitis (AP), but the results are inconclusive. We conducted this cumulative meta-analysis for a precise estimate of the relationship between IL-8 rs4073 polymorphism and acute pancreatitis. METHODS: We searched the electronic databases for relevant studies. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the associations. For a better presentation of how the pooled ORs changed as updated evidence accumulated, we used forest plots from a cumulative meta-analysis method. RESULTS: Ten studies involving 1646 AP patients and 1816 controls were finally included in this meta-analysis. Cumulative meta-analyses indicated there is a consistent trend toward association after the initial discovery. Under the allelic, dominant, recessive and homozygous models, the pooled ORs were 1.265 (1.147–1.395, p < 0.001), 1.304 (1.127–1.508, p < 0.001), 1.431 (1.203–1.702, p < 0.001), and 1.634 (1.334–2.001, p < 0.001), respectively. CONCLUSIONS: This meta-analysis demonstrated a suggestive result that people who carried the risk A allele of the IL-8 rs4073 polymorphism may be more sensitive to acute pancreatitis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-019-0861-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6657145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66571452019-07-31 Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis Li, Yening Bai, Jing He, Bing Wang, Nan Wang, Haoran Liu, Dongliang BMC Med Genet Research Article BACKGROUND: Several studies have been performed to investigate the associations between interleukin (IL)-8 rs4073 polymorphism and acute pancreatitis (AP), but the results are inconclusive. We conducted this cumulative meta-analysis for a precise estimate of the relationship between IL-8 rs4073 polymorphism and acute pancreatitis. METHODS: We searched the electronic databases for relevant studies. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the associations. For a better presentation of how the pooled ORs changed as updated evidence accumulated, we used forest plots from a cumulative meta-analysis method. RESULTS: Ten studies involving 1646 AP patients and 1816 controls were finally included in this meta-analysis. Cumulative meta-analyses indicated there is a consistent trend toward association after the initial discovery. Under the allelic, dominant, recessive and homozygous models, the pooled ORs were 1.265 (1.147–1.395, p < 0.001), 1.304 (1.127–1.508, p < 0.001), 1.431 (1.203–1.702, p < 0.001), and 1.634 (1.334–2.001, p < 0.001), respectively. CONCLUSIONS: This meta-analysis demonstrated a suggestive result that people who carried the risk A allele of the IL-8 rs4073 polymorphism may be more sensitive to acute pancreatitis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-019-0861-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-24 /pmc/articles/PMC6657145/ /pubmed/31340771 http://dx.doi.org/10.1186/s12881-019-0861-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Li, Yening Bai, Jing He, Bing Wang, Nan Wang, Haoran Liu, Dongliang Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title | Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title_full | Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title_fullStr | Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title_full_unstemmed | Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title_short | Weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
title_sort | weak association between the interleukin-8 rs4073 polymorphism and acute pancreatitis: a cumulative meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657145/ https://www.ncbi.nlm.nih.gov/pubmed/31340771 http://dx.doi.org/10.1186/s12881-019-0861-4 |
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