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TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis
BACKGROUND: TIM-family proteins are expressed on different immune cells such as dendritic cells, macrophages, type 1 and 2 T helper (Th) cells. Therefore, they have the ability to contribute to the various intracellular signals and immune responses, importantly the regulation of Th1 and Th17 cell di...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366744/ https://www.ncbi.nlm.nih.gov/pubmed/30730912 http://dx.doi.org/10.1371/journal.pone.0211146 |
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author | Razi, Bahman Reykandeh, Samira Esmaeili Alizadeh, Shahab Amirzargar, AliAkbar Saghazadeh, Amene Rezaei, Nima |
author_facet | Razi, Bahman Reykandeh, Samira Esmaeili Alizadeh, Shahab Amirzargar, AliAkbar Saghazadeh, Amene Rezaei, Nima |
author_sort | Razi, Bahman |
collection | PubMed |
description | BACKGROUND: TIM-family proteins are expressed on different immune cells such as dendritic cells, macrophages, type 1 and 2 T helper (Th) cells. Therefore, they have the ability to contribute to the various intracellular signals and immune responses, importantly the regulation of Th1 and Th17 cell differentiation, which plays a remarked role in fight against inflammatory and autoimmune diseases. Association of TIM family gene polymorphisms with rheumatoid arthritis (RA) has been frequently investigated. The findings however are not entirely consistent. Therefore, we carried out the present meta-analysis to examine the association between RA and the following TIM family gene polymorphisms: rs41297579, rs1036199, rs10515746, and rs7700944. METHODS: A systematic search of Scopus, PubMed, and Web of Science databases was conducted through December 2018. Combined odds ratios (OR) with their corresponding 95% confidence intervals (CI) were calculated under different possible genetic models. RESULTS: A total of eight case-control studies were included in the present meta-analysis. The results demonstrated significant association of RA with TIM-3 rs1036199 polymorphism under dominant (OR, 1.93, 95% CI, 1.43–2.61) and allelic models (OR, 1.74, 95% CI, 1.31–2.30). None of the other examined polymorphisms indicated significant association with RA. CONCLUSIONS: The present meta-analysis revealed that the TIM-3 rs1036199 polymorphism might confer susceptibility to RA. Further studies are required to reassert our findings. |
format | Online Article Text |
id | pubmed-6366744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63667442019-02-22 TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis Razi, Bahman Reykandeh, Samira Esmaeili Alizadeh, Shahab Amirzargar, AliAkbar Saghazadeh, Amene Rezaei, Nima PLoS One Research Article BACKGROUND: TIM-family proteins are expressed on different immune cells such as dendritic cells, macrophages, type 1 and 2 T helper (Th) cells. Therefore, they have the ability to contribute to the various intracellular signals and immune responses, importantly the regulation of Th1 and Th17 cell differentiation, which plays a remarked role in fight against inflammatory and autoimmune diseases. Association of TIM family gene polymorphisms with rheumatoid arthritis (RA) has been frequently investigated. The findings however are not entirely consistent. Therefore, we carried out the present meta-analysis to examine the association between RA and the following TIM family gene polymorphisms: rs41297579, rs1036199, rs10515746, and rs7700944. METHODS: A systematic search of Scopus, PubMed, and Web of Science databases was conducted through December 2018. Combined odds ratios (OR) with their corresponding 95% confidence intervals (CI) were calculated under different possible genetic models. RESULTS: A total of eight case-control studies were included in the present meta-analysis. The results demonstrated significant association of RA with TIM-3 rs1036199 polymorphism under dominant (OR, 1.93, 95% CI, 1.43–2.61) and allelic models (OR, 1.74, 95% CI, 1.31–2.30). None of the other examined polymorphisms indicated significant association with RA. CONCLUSIONS: The present meta-analysis revealed that the TIM-3 rs1036199 polymorphism might confer susceptibility to RA. Further studies are required to reassert our findings. Public Library of Science 2019-02-07 /pmc/articles/PMC6366744/ /pubmed/30730912 http://dx.doi.org/10.1371/journal.pone.0211146 Text en © 2019 Razi 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Razi, Bahman Reykandeh, Samira Esmaeili Alizadeh, Shahab Amirzargar, AliAkbar Saghazadeh, Amene Rezaei, Nima TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title | TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title_full | TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title_fullStr | TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title_full_unstemmed | TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title_short | TIM family gene polymorphism and susceptibility to rheumatoid arthritis: Systematic review and meta-analysis |
title_sort | tim family gene polymorphism and susceptibility to rheumatoid arthritis: systematic review and meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366744/ https://www.ncbi.nlm.nih.gov/pubmed/30730912 http://dx.doi.org/10.1371/journal.pone.0211146 |
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