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MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease
INTRODUCTION: The current study was designed to analyze whether polymorphisms of miR-146a and miR-155 are related to Behçet’s disease (BD) in the Egyptian population. MATERIAL AND METHODS: A total of 96 unrelated BD patients and 100 healthy subjects were genotyped for miR-146a (rs2910164) and miR-15...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Termedia Publishing House
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710268/ https://www.ncbi.nlm.nih.gov/pubmed/36457982 http://dx.doi.org/10.5114/aoms/105349 |
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author | Shaker, Olfat G. Abdelaleem, Omayma O. Fouad, Nermeen A. Ahmed, Naglaa A. Hussein, Hoda A. Ibrahem, Enas G. Mohamed, Abdelrahmaan A. Ahmed, Othman M. Ali, Doaa Y. |
author_facet | Shaker, Olfat G. Abdelaleem, Omayma O. Fouad, Nermeen A. Ahmed, Naglaa A. Hussein, Hoda A. Ibrahem, Enas G. Mohamed, Abdelrahmaan A. Ahmed, Othman M. Ali, Doaa Y. |
author_sort | Shaker, Olfat G. |
collection | PubMed |
description | INTRODUCTION: The current study was designed to analyze whether polymorphisms of miR-146a and miR-155 are related to Behçet’s disease (BD) in the Egyptian population. MATERIAL AND METHODS: A total of 96 unrelated BD patients and 100 healthy subjects were genotyped for miR-146a (rs2910164) and miR-155 (rs767649) using real-time polymerase chain reaction. RESULTS: The results showed significant elevation in the frequency of rs2910164 GG and CC genotypes in BD patients compared with controls (adjusted OR = 22.156, 95% CI: 4.728–103.818; p < 0.001 and adjusted OR = 40.358, 95% CI: 8.928–182.440; p < 0.001, respectively). Also, the rs2910164 G allele conferred a higher risk of developing BD (adjusted OR = 3.665, 95% CI: 2.013–6.671; p < 0.001). MiR-146a (rs2910164) polymorphism was a risk factor for susceptibility to BD in dominant, recessive and additive models of inheritance (all p < 0.001), while the miR-155 (rs767649) polymorphism was a risk factor in the recessive model only (p = 0.021). GG and CG genotypes of rs2910164 were associated with higher Behcet’s disease current activity index (BDCAI) and ocular involvement compared with CC genotype (p = 0.005 and p = 0.004, respectively). Genotype AT of rs767649 was related to higher BDCAI (p = 0.026) compared with TT and AA genotypes. CONCLUSIONS: miR-146a (rs2910164) and miR-155 (rs767649) are likely to play an important role in the Egyptian population in development of BD and also influence disease severity. |
format | Online Article Text |
id | pubmed-9710268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-97102682022-11-30 MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease Shaker, Olfat G. Abdelaleem, Omayma O. Fouad, Nermeen A. Ahmed, Naglaa A. Hussein, Hoda A. Ibrahem, Enas G. Mohamed, Abdelrahmaan A. Ahmed, Othman M. Ali, Doaa Y. Arch Med Sci Clinical Research INTRODUCTION: The current study was designed to analyze whether polymorphisms of miR-146a and miR-155 are related to Behçet’s disease (BD) in the Egyptian population. MATERIAL AND METHODS: A total of 96 unrelated BD patients and 100 healthy subjects were genotyped for miR-146a (rs2910164) and miR-155 (rs767649) using real-time polymerase chain reaction. RESULTS: The results showed significant elevation in the frequency of rs2910164 GG and CC genotypes in BD patients compared with controls (adjusted OR = 22.156, 95% CI: 4.728–103.818; p < 0.001 and adjusted OR = 40.358, 95% CI: 8.928–182.440; p < 0.001, respectively). Also, the rs2910164 G allele conferred a higher risk of developing BD (adjusted OR = 3.665, 95% CI: 2.013–6.671; p < 0.001). MiR-146a (rs2910164) polymorphism was a risk factor for susceptibility to BD in dominant, recessive and additive models of inheritance (all p < 0.001), while the miR-155 (rs767649) polymorphism was a risk factor in the recessive model only (p = 0.021). GG and CG genotypes of rs2910164 were associated with higher Behcet’s disease current activity index (BDCAI) and ocular involvement compared with CC genotype (p = 0.005 and p = 0.004, respectively). Genotype AT of rs767649 was related to higher BDCAI (p = 0.026) compared with TT and AA genotypes. CONCLUSIONS: miR-146a (rs2910164) and miR-155 (rs767649) are likely to play an important role in the Egyptian population in development of BD and also influence disease severity. Termedia Publishing House 2021-03-19 /pmc/articles/PMC9710268/ /pubmed/36457982 http://dx.doi.org/10.5114/aoms/105349 Text en Copyright: © 2021 Termedia & Banach https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Shaker, Olfat G. Abdelaleem, Omayma O. Fouad, Nermeen A. Ahmed, Naglaa A. Hussein, Hoda A. Ibrahem, Enas G. Mohamed, Abdelrahmaan A. Ahmed, Othman M. Ali, Doaa Y. MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title | MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title_full | MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title_fullStr | MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title_full_unstemmed | MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title_short | MiR-146a and miR-155 polymorphisms in Egyptian patients with Behcet’s disease |
title_sort | mir-146a and mir-155 polymorphisms in egyptian patients with behcet’s disease |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710268/ https://www.ncbi.nlm.nih.gov/pubmed/36457982 http://dx.doi.org/10.5114/aoms/105349 |
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