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TLR4 polymorphism and periodontitis susceptibility: A meta-analysis

BACKGROUND: Many primary and secondary studies reported the association between Toll-like receptor 4 (TLR4) polymorphism and periodontitis susceptibility, which mainly focused on TLR4–299A>G or TLR4–399C>T of Caucasian, however, these studies had different conclusions. The aim of this study wa...

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Autores principales: Jin, Su-Han, Guan, Xiao-Yan, Liang, Wen-Hong, Bai, Guo-Hui, Liu, Jian-Guo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023927/
https://www.ncbi.nlm.nih.gov/pubmed/27603404
http://dx.doi.org/10.1097/MD.0000000000004845
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author Jin, Su-Han
Guan, Xiao-Yan
Liang, Wen-Hong
Bai, Guo-Hui
Liu, Jian-Guo
author_facet Jin, Su-Han
Guan, Xiao-Yan
Liang, Wen-Hong
Bai, Guo-Hui
Liu, Jian-Guo
author_sort Jin, Su-Han
collection PubMed
description BACKGROUND: Many primary and secondary studies reported the association between Toll-like receptor 4 (TLR4) polymorphism and periodontitis susceptibility, which mainly focused on TLR4–299A>G or TLR4–399C>T of Caucasian, however, these studies had different conclusions. The aim of this study was to reassess relative studies about TLR4 polymorphism and periodontitis susceptibility, and update meta-analysis. METHODS: We searched the electronic database including CNKI (Chinese National Knowledge Infrastructure), PubMed, Embase, and hand searched relative studies until January 4, 2016. Two authors selected studies according to inclusion and exclusion criteria, assessed studies using Newcastle-Ottawa Scale case control study (NOS), and calculated the combined effect size using STATA software, version 12.0. RESULTS: This meta-analysis included 18 studies, containing 2453 healthy participants and 2987 patients with chronic periodontitis (CP) and 462 patients with aggressive periodontitis (AP). There was a significance between TLR4C>G (rs7873784) allele and CP in Asian, and its recessive model was also significant (for C vs G: odds ratio [OR] = 0.72, 95% confidence interval [CI] = 0.54–0.95, I(2) = 0%; for CC + CG vs GG: OR = 0.66, 95% CI = 0.49–0.89, I(2) = 0%). However, we did not detect any significant relevance between other TLR4 polymorphism and periodontitis susceptibility in overall and subgroup analyses. The sensitive analysis showed that dropping any single studies did not affect the pooled-analysis results. Publication bias was not detected. CONCLUSIONS: The meta-analysis found association between TLR4C>G (rs7873784) allele and CP in Asian and it may passed on to offsprings in the form of recessiveness. However, further studies about the association between TLR4C>G (rs7873784) and CP is warranted to confirm.
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spelling pubmed-50239272016-09-26 TLR4 polymorphism and periodontitis susceptibility: A meta-analysis Jin, Su-Han Guan, Xiao-Yan Liang, Wen-Hong Bai, Guo-Hui Liu, Jian-Guo Medicine (Baltimore) 5900 BACKGROUND: Many primary and secondary studies reported the association between Toll-like receptor 4 (TLR4) polymorphism and periodontitis susceptibility, which mainly focused on TLR4–299A>G or TLR4–399C>T of Caucasian, however, these studies had different conclusions. The aim of this study was to reassess relative studies about TLR4 polymorphism and periodontitis susceptibility, and update meta-analysis. METHODS: We searched the electronic database including CNKI (Chinese National Knowledge Infrastructure), PubMed, Embase, and hand searched relative studies until January 4, 2016. Two authors selected studies according to inclusion and exclusion criteria, assessed studies using Newcastle-Ottawa Scale case control study (NOS), and calculated the combined effect size using STATA software, version 12.0. RESULTS: This meta-analysis included 18 studies, containing 2453 healthy participants and 2987 patients with chronic periodontitis (CP) and 462 patients with aggressive periodontitis (AP). There was a significance between TLR4C>G (rs7873784) allele and CP in Asian, and its recessive model was also significant (for C vs G: odds ratio [OR] = 0.72, 95% confidence interval [CI] = 0.54–0.95, I(2) = 0%; for CC + CG vs GG: OR = 0.66, 95% CI = 0.49–0.89, I(2) = 0%). However, we did not detect any significant relevance between other TLR4 polymorphism and periodontitis susceptibility in overall and subgroup analyses. The sensitive analysis showed that dropping any single studies did not affect the pooled-analysis results. Publication bias was not detected. CONCLUSIONS: The meta-analysis found association between TLR4C>G (rs7873784) allele and CP in Asian and it may passed on to offsprings in the form of recessiveness. However, further studies about the association between TLR4C>G (rs7873784) and CP is warranted to confirm. Wolters Kluwer Health 2016-09-09 /pmc/articles/PMC5023927/ /pubmed/27603404 http://dx.doi.org/10.1097/MD.0000000000004845 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-No Derivatives 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 5900
Jin, Su-Han
Guan, Xiao-Yan
Liang, Wen-Hong
Bai, Guo-Hui
Liu, Jian-Guo
TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title_full TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title_fullStr TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title_full_unstemmed TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title_short TLR4 polymorphism and periodontitis susceptibility: A meta-analysis
title_sort tlr4 polymorphism and periodontitis susceptibility: a meta-analysis
topic 5900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023927/
https://www.ncbi.nlm.nih.gov/pubmed/27603404
http://dx.doi.org/10.1097/MD.0000000000004845
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