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A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease

Background: The level of interleukin-6 (IL-6) and its gene polymorphism are associated with the end-stage renal disease (ESRD) and the related complications. This study aimed to investigate the correction between IL-6 -174G/C polymorphism and ESRD by meta-analysis. Methods: Using the databases inclu...

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Autores principales: Feng, Ye, Tang, Yan, Zhou, Hongwei, Xie, Kaiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014497/
https://www.ncbi.nlm.nih.gov/pubmed/28164733
http://dx.doi.org/10.1080/0886022X.2017.1281146
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author Feng, Ye
Tang, Yan
Zhou, Hongwei
Xie, Kaiqing
author_facet Feng, Ye
Tang, Yan
Zhou, Hongwei
Xie, Kaiqing
author_sort Feng, Ye
collection PubMed
description Background: The level of interleukin-6 (IL-6) and its gene polymorphism are associated with the end-stage renal disease (ESRD) and the related complications. This study aimed to investigate the correction between IL-6 -174G/C polymorphism and ESRD by meta-analysis. Methods: Using the databases including PubMed, Embase, Cochrane library, CNKI, and CBM, the data of case-control studies on correlation between IL-6 -174G/C polymorphism and ESRD from database establishment to January 2016 were collected. According to inclusion and exclusion criteria, the quality of literatures was evaluated. The relevant research data were extracted, followed by meta-analysis using Revman 5.3 software (London, UK). The combined odds ratio (OR) and 95% confidence interval (95%CI) of each genetic model were calculated, and the publication bias data was assessed using the Stata 12.0 software (College Station, TX). Results: A total of five literatures were included, with 1199 cases in case group and 1089 cases in control group. Meta-analysis showed that, there was no significant correlation between each genetic model of IL-6 -174G/C polymorphism and ESRD [(C versus G): OR = 1.36, 95%CI (0.69, 2.66), p = .38; (CC + GC versus GG): OR = 1.28, 95%CI (0.58, 2.82), p = .54; (CC versus GG + GC): OR = 1.71, 95%CI (0.82, 3.54), p = .15; (CC versus GG): OR = 1.74, 95%CI (0.76, 3.99), p = .19; (GC versus GG): OR = 1.18, 95%CI (0.55, 2.54), p = .67]. The race subgroup analysis showed that, there was no significant correlation between each genetic model of IL-6 -174G/C polymorphism and ESRD in the Caucasians (p > .05). Conclusion: IL-6 -174G/C polymorphism has no significant correlation with the susceptibility risk of ESRD, and may not be a risk factor for ESRD.
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spelling pubmed-60144972018-06-28 A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease Feng, Ye Tang, Yan Zhou, Hongwei Xie, Kaiqing Ren Fail Clinical Study Background: The level of interleukin-6 (IL-6) and its gene polymorphism are associated with the end-stage renal disease (ESRD) and the related complications. This study aimed to investigate the correction between IL-6 -174G/C polymorphism and ESRD by meta-analysis. Methods: Using the databases including PubMed, Embase, Cochrane library, CNKI, and CBM, the data of case-control studies on correlation between IL-6 -174G/C polymorphism and ESRD from database establishment to January 2016 were collected. According to inclusion and exclusion criteria, the quality of literatures was evaluated. The relevant research data were extracted, followed by meta-analysis using Revman 5.3 software (London, UK). The combined odds ratio (OR) and 95% confidence interval (95%CI) of each genetic model were calculated, and the publication bias data was assessed using the Stata 12.0 software (College Station, TX). Results: A total of five literatures were included, with 1199 cases in case group and 1089 cases in control group. Meta-analysis showed that, there was no significant correlation between each genetic model of IL-6 -174G/C polymorphism and ESRD [(C versus G): OR = 1.36, 95%CI (0.69, 2.66), p = .38; (CC + GC versus GG): OR = 1.28, 95%CI (0.58, 2.82), p = .54; (CC versus GG + GC): OR = 1.71, 95%CI (0.82, 3.54), p = .15; (CC versus GG): OR = 1.74, 95%CI (0.76, 3.99), p = .19; (GC versus GG): OR = 1.18, 95%CI (0.55, 2.54), p = .67]. The race subgroup analysis showed that, there was no significant correlation between each genetic model of IL-6 -174G/C polymorphism and ESRD in the Caucasians (p > .05). Conclusion: IL-6 -174G/C polymorphism has no significant correlation with the susceptibility risk of ESRD, and may not be a risk factor for ESRD. Taylor & Francis 2017-02-05 /pmc/articles/PMC6014497/ /pubmed/28164733 http://dx.doi.org/10.1080/0886022X.2017.1281146 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Feng, Ye
Tang, Yan
Zhou, Hongwei
Xie, Kaiqing
A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title_full A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title_fullStr A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title_full_unstemmed A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title_short A meta-analysis on correlation between interleukin-6 -174G/C polymorphism and end-stage renal disease
title_sort meta-analysis on correlation between interleukin-6 -174g/c polymorphism and end-stage renal disease
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014497/
https://www.ncbi.nlm.nih.gov/pubmed/28164733
http://dx.doi.org/10.1080/0886022X.2017.1281146
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