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Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study

BACKGROUND: The toll-like receptor (TLR)4-interleukin1β (IL1β) signaling pathway is involved in the monosodium urate (MSU)-mediated inflammation. The aim of this present study was to determine whether the TLR4 gene rs2149356 SNP is associated with gouty arthritis (GA) susceptibility and whether rs21...

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Autores principales: Qing, Yu-Feng, Zhou, Jing-Guo, Zhang, Quan-Bo, Wang, Dong-Sheng, Li, Min, Yang, Qi-Bin, Huang, Cui-Ping, Yin, Ling, Pan, Shu-Yue, Xie, Wen-Guang, Zhang, Meng-Yun, Pu, Meng-Jun, Zeng, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667827/
https://www.ncbi.nlm.nih.gov/pubmed/23738004
http://dx.doi.org/10.1371/journal.pone.0064845
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author Qing, Yu-Feng
Zhou, Jing-Guo
Zhang, Quan-Bo
Wang, Dong-Sheng
Li, Min
Yang, Qi-Bin
Huang, Cui-Ping
Yin, Ling
Pan, Shu-Yue
Xie, Wen-Guang
Zhang, Meng-Yun
Pu, Meng-Jun
Zeng, Mei
author_facet Qing, Yu-Feng
Zhou, Jing-Guo
Zhang, Quan-Bo
Wang, Dong-Sheng
Li, Min
Yang, Qi-Bin
Huang, Cui-Ping
Yin, Ling
Pan, Shu-Yue
Xie, Wen-Guang
Zhang, Meng-Yun
Pu, Meng-Jun
Zeng, Mei
author_sort Qing, Yu-Feng
collection PubMed
description BACKGROUND: The toll-like receptor (TLR)4-interleukin1β (IL1β) signaling pathway is involved in the monosodium urate (MSU)-mediated inflammation. The aim of this present study was to determine whether the TLR4 gene rs2149356 SNP is associated with gouty arthritis (GA) susceptibility and whether rs2149356 SNP impacts the TLR4-IL1β signaling pathway molecules expression. METHODS AND FINDINGS: The rs2149356 SNP was detected in 459 GA patients and 669 control subjects (containing 459 healthy and 210 hyperuricemic subjects). Peripheral blood mononuclear cells (PBMCs) TLR4 mRNA and serum IL1β were measured in different genotype carriers, and correlations between TLR4 gene SNP and TLR4 mRNA, IL1β were investigated. The frequencies of the genotype and allele were significantly different between the GA and control groups (P<0.01, respectively). The TT genotype was associated with a significantly increased risk of GA (OR = 1.88); this finding was not influenced by making adjustments for the components of possible confounders (adjusted OR = 1.96). TLR4 mRNA and IL1β were significantly increased in the TT genotype from acute GA patients (P<0.05, respectively), and lipids were significantly different among three genotypes in the GA patients (P<0.05, respectively). CONCLUSIONS: The TLR4 gene rs2149356 SNP might be associated with GA susceptibility, and might participate in regulating immune, inflammation and lipid metabolism. Further studies are required to confirm these findings.
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spelling pubmed-36678272013-06-04 Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study Qing, Yu-Feng Zhou, Jing-Guo Zhang, Quan-Bo Wang, Dong-Sheng Li, Min Yang, Qi-Bin Huang, Cui-Ping Yin, Ling Pan, Shu-Yue Xie, Wen-Guang Zhang, Meng-Yun Pu, Meng-Jun Zeng, Mei PLoS One Research Article BACKGROUND: The toll-like receptor (TLR)4-interleukin1β (IL1β) signaling pathway is involved in the monosodium urate (MSU)-mediated inflammation. The aim of this present study was to determine whether the TLR4 gene rs2149356 SNP is associated with gouty arthritis (GA) susceptibility and whether rs2149356 SNP impacts the TLR4-IL1β signaling pathway molecules expression. METHODS AND FINDINGS: The rs2149356 SNP was detected in 459 GA patients and 669 control subjects (containing 459 healthy and 210 hyperuricemic subjects). Peripheral blood mononuclear cells (PBMCs) TLR4 mRNA and serum IL1β were measured in different genotype carriers, and correlations between TLR4 gene SNP and TLR4 mRNA, IL1β were investigated. The frequencies of the genotype and allele were significantly different between the GA and control groups (P<0.01, respectively). The TT genotype was associated with a significantly increased risk of GA (OR = 1.88); this finding was not influenced by making adjustments for the components of possible confounders (adjusted OR = 1.96). TLR4 mRNA and IL1β were significantly increased in the TT genotype from acute GA patients (P<0.05, respectively), and lipids were significantly different among three genotypes in the GA patients (P<0.05, respectively). CONCLUSIONS: The TLR4 gene rs2149356 SNP might be associated with GA susceptibility, and might participate in regulating immune, inflammation and lipid metabolism. Further studies are required to confirm these findings. Public Library of Science 2013-05-30 /pmc/articles/PMC3667827/ /pubmed/23738004 http://dx.doi.org/10.1371/journal.pone.0064845 Text en © 2013 Qing et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Qing, Yu-Feng
Zhou, Jing-Guo
Zhang, Quan-Bo
Wang, Dong-Sheng
Li, Min
Yang, Qi-Bin
Huang, Cui-Ping
Yin, Ling
Pan, Shu-Yue
Xie, Wen-Guang
Zhang, Meng-Yun
Pu, Meng-Jun
Zeng, Mei
Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title_full Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title_fullStr Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title_full_unstemmed Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title_short Association of TLR4 Gene rs2149356 Polymorphism with Primary Gouty Arthritis in a Case-Control Study
title_sort association of tlr4 gene rs2149356 polymorphism with primary gouty arthritis in a case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667827/
https://www.ncbi.nlm.nih.gov/pubmed/23738004
http://dx.doi.org/10.1371/journal.pone.0064845
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