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Genetic polymorphisms in pattern recognition receptors and risk of periodontitis: Evidence based on 12,793 subjects

Abstract Pattern recognition receptors (PRRs) constitute a pivotal arm of innate immunity. Many studies investigated the association between PRRs polymorphisms and periodontitis risk, which showed inconclusive results. The aim of the meta-analysis was to evaluate the precise association between five...

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Published in:Human immunology 2015-07, Vol.76 (7), p.496-504
Main Authors: Han, Min-xuan, Ding, Cheng, Kyung, Hee-Moon
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creator Han, Min-xuan
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Kyung, Hee-Moon
description Abstract Pattern recognition receptors (PRRs) constitute a pivotal arm of innate immunity. Many studies investigated the association between PRRs polymorphisms and periodontitis risk, which showed inconclusive results. The aim of the meta-analysis was to evaluate the precise association between five widely-evaluated polymorphisms ( CD14 −260C/T (rs2569190), Toll-like receptor ( TLR ) 2 2408G/A (rs5743708), TLR4 896A/G (rs4986790), TLR4 1196C/T (rs4986791), mannose-binding lectin ( MBL ) codon 54 (rs1800450)) within the PRRs and susceptibility to either chronic (CP) or aggressive periodontitis (AgP). Overall, no significant association was found for the PRRs polymorphisms with either CP or AgP. In the subgroup analyses, TLR4 896G and 1196T alleles yielded a 32% (OR = 1.32, 95% CI: 1.04–1.68) and a 37% increased CP risk (OR = 1.37, 95% CI: 1.05–1.80) in Caucasians, respectively. Further stratified analyses revealed links between CD14 , MBL2 polymorphisms and the severity of CP. This meta-analysis suggested that the periodontitis susceptibility was partly controlled by PRRs polymorphisms involved in the innate immunity.
doi_str_mv 10.1016/j.humimm.2015.06.006
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Many studies investigated the association between PRRs polymorphisms and periodontitis risk, which showed inconclusive results. The aim of the meta-analysis was to evaluate the precise association between five widely-evaluated polymorphisms ( CD14 −260C/T (rs2569190), Toll-like receptor ( TLR ) 2 2408G/A (rs5743708), TLR4 896A/G (rs4986790), TLR4 1196C/T (rs4986791), mannose-binding lectin ( MBL ) codon 54 (rs1800450)) within the PRRs and susceptibility to either chronic (CP) or aggressive periodontitis (AgP). Overall, no significant association was found for the PRRs polymorphisms with either CP or AgP. In the subgroup analyses, TLR4 896G and 1196T alleles yielded a 32% (OR = 1.32, 95% CI: 1.04–1.68) and a 37% increased CP risk (OR = 1.37, 95% CI: 1.05–1.80) in Caucasians, respectively. Further stratified analyses revealed links between CD14 , MBL2 polymorphisms and the severity of CP. 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Many studies investigated the association between PRRs polymorphisms and periodontitis risk, which showed inconclusive results. The aim of the meta-analysis was to evaluate the precise association between five widely-evaluated polymorphisms ( CD14 −260C/T (rs2569190), Toll-like receptor ( TLR ) 2 2408G/A (rs5743708), TLR4 896A/G (rs4986790), TLR4 1196C/T (rs4986791), mannose-binding lectin ( MBL ) codon 54 (rs1800450)) within the PRRs and susceptibility to either chronic (CP) or aggressive periodontitis (AgP). Overall, no significant association was found for the PRRs polymorphisms with either CP or AgP. In the subgroup analyses, TLR4 896G and 1196T alleles yielded a 32% (OR = 1.32, 95% CI: 1.04–1.68) and a 37% increased CP risk (OR = 1.37, 95% CI: 1.05–1.80) in Caucasians, respectively. Further stratified analyses revealed links between CD14 , MBL2 polymorphisms and the severity of CP. 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Many studies investigated the association between PRRs polymorphisms and periodontitis risk, which showed inconclusive results. The aim of the meta-analysis was to evaluate the precise association between five widely-evaluated polymorphisms ( CD14 −260C/T (rs2569190), Toll-like receptor ( TLR ) 2 2408G/A (rs5743708), TLR4 896A/G (rs4986790), TLR4 1196C/T (rs4986791), mannose-binding lectin ( MBL ) codon 54 (rs1800450)) within the PRRs and susceptibility to either chronic (CP) or aggressive periodontitis (AgP). Overall, no significant association was found for the PRRs polymorphisms with either CP or AgP. In the subgroup analyses, TLR4 896G and 1196T alleles yielded a 32% (OR = 1.32, 95% CI: 1.04–1.68) and a 37% increased CP risk (OR = 1.37, 95% CI: 1.05–1.80) in Caucasians, respectively. Further stratified analyses revealed links between CD14 , MBL2 polymorphisms and the severity of CP. This meta-analysis suggested that the periodontitis susceptibility was partly controlled by PRRs polymorphisms involved in the innate immunity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26079505</pmid><doi>10.1016/j.humimm.2015.06.006</doi><tpages>9</tpages></addata></record>
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subjects Allergy and Immunology
CD14
Gene polymorphisms
Genetic Predisposition to Disease
Humans
Lipopolysaccharide Receptors - genetics
Mannose-binding lectin
Mannose-Binding Lectin - genetics
Periodontitis
Periodontitis - etiology
Periodontitis - genetics
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Publication Bias
Receptors, Pattern Recognition - genetics
Risk
Toll-Like Receptor 4 - genetics
Toll-like receptors
title Genetic polymorphisms in pattern recognition receptors and risk of periodontitis: Evidence based on 12,793 subjects
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