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Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey
INTRODUCTION: In this study, we aimed to determine the frequency of MEFV mutations in Behçet’s disease (BD) and to investigate the relationship between clinical findings of the disease and the MEFV mutations. MATERIAL AND METHODS: A total of 66 participants (30 BD patients, 36 healthy subjects) were...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301670/ https://www.ncbi.nlm.nih.gov/pubmed/35875715 http://dx.doi.org/10.5114/reum.2022.117843 |
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author | Serarslan, Gamze Cura, Sibel Elmacıoğlu Kimyon, Gezmiş Üçgül, Gökhan Karadağ, Mehmet |
author_facet | Serarslan, Gamze Cura, Sibel Elmacıoğlu Kimyon, Gezmiş Üçgül, Gökhan Karadağ, Mehmet |
author_sort | Serarslan, Gamze |
collection | PubMed |
description | INTRODUCTION: In this study, we aimed to determine the frequency of MEFV mutations in Behçet’s disease (BD) and to investigate the relationship between clinical findings of the disease and the MEFV mutations. MATERIAL AND METHODS: A total of 66 participants (30 BD patients, 36 healthy subjects) were included in this study. The MEFV gene was analyzed by using DNA sequence analysis. RESULTS: The distribution of MEFV mutations was not significantly different between the patients and the control group (p = 0.373). However, individuals with R202Q mutation had a risk of OR 4 times (95% CI: 1.1–14.5) higher than those without the mutation (p = 0.035). The rate of vascular involvement was statistically significantly higher in patients with the mutation than in patients without the mutation (p = 0.005). CONCLUSIONS: MEFV mutation was associated with vascular involvement in patients with BD. This is also the first study to indicate that the R202Q mutation may have a role in BD. However large series from different regions are required to compare these results. |
format | Online Article Text |
id | pubmed-9301670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie |
record_format | MEDLINE/PubMed |
spelling | pubmed-93016702022-07-22 Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey Serarslan, Gamze Cura, Sibel Elmacıoğlu Kimyon, Gezmiş Üçgül, Gökhan Karadağ, Mehmet Reumatologia Original Paper INTRODUCTION: In this study, we aimed to determine the frequency of MEFV mutations in Behçet’s disease (BD) and to investigate the relationship between clinical findings of the disease and the MEFV mutations. MATERIAL AND METHODS: A total of 66 participants (30 BD patients, 36 healthy subjects) were included in this study. The MEFV gene was analyzed by using DNA sequence analysis. RESULTS: The distribution of MEFV mutations was not significantly different between the patients and the control group (p = 0.373). However, individuals with R202Q mutation had a risk of OR 4 times (95% CI: 1.1–14.5) higher than those without the mutation (p = 0.035). The rate of vascular involvement was statistically significantly higher in patients with the mutation than in patients without the mutation (p = 0.005). CONCLUSIONS: MEFV mutation was associated with vascular involvement in patients with BD. This is also the first study to indicate that the R202Q mutation may have a role in BD. However large series from different regions are required to compare these results. Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2022-07-13 2022 /pmc/articles/PMC9301670/ /pubmed/35875715 http://dx.doi.org/10.5114/reum.2022.117843 Text en Copyright: © 2022 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 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 | Original Paper Serarslan, Gamze Cura, Sibel Elmacıoğlu Kimyon, Gezmiş Üçgül, Gökhan Karadağ, Mehmet Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title | Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title_full | Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title_fullStr | Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title_full_unstemmed | Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title_short | Association of MEFV mutations and vascular involvement in Behçet’s disease: a study from Hatay, Turkey |
title_sort | association of mefv mutations and vascular involvement in behçet’s disease: a study from hatay, turkey |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301670/ https://www.ncbi.nlm.nih.gov/pubmed/35875715 http://dx.doi.org/10.5114/reum.2022.117843 |
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