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FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis

Rheumatoid arthritis (RA) is a chronic autoimmune disease that, when improperly treated, leads to disability in patients. Various factors that may cause the development and activity of RA are being considered. Epigenetic factors are also receiving increasing attention. In our study, we analyzed the...

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Autores principales: Podgórska, Dominika, Cieśla, Marek, Kolarz, Bogdan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410058/
https://www.ncbi.nlm.nih.gov/pubmed/36012903
http://dx.doi.org/10.3390/jcm11164664
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author Podgórska, Dominika
Cieśla, Marek
Kolarz, Bogdan
author_facet Podgórska, Dominika
Cieśla, Marek
Kolarz, Bogdan
author_sort Podgórska, Dominika
collection PubMed
description Rheumatoid arthritis (RA) is a chronic autoimmune disease that, when improperly treated, leads to disability in patients. Various factors that may cause the development and activity of RA are being considered. Epigenetic factors are also receiving increasing attention. In our study, we analyzed the association between FCER1G gene methylation and RA activity. We conducted our study in 50 RA patients and 24 controls. The patients were divided into two groups in terms of high disease activity and remission. Quantitative real-time methylation-specific PCR was used to analyze the methylation status of the investigated genes. We observed that RA patients have lower levels of methylation of the FCER1G gene compared to controls, but we did not find any difference in the methylation status of this gene between patients with high disease activity and remission. The results of this study suggest that FCER1G gene methylation may be a new potential epigenetic marker of RA that is independent of disease activity.
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spelling pubmed-94100582022-08-26 FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis Podgórska, Dominika Cieśla, Marek Kolarz, Bogdan J Clin Med Article Rheumatoid arthritis (RA) is a chronic autoimmune disease that, when improperly treated, leads to disability in patients. Various factors that may cause the development and activity of RA are being considered. Epigenetic factors are also receiving increasing attention. In our study, we analyzed the association between FCER1G gene methylation and RA activity. We conducted our study in 50 RA patients and 24 controls. The patients were divided into two groups in terms of high disease activity and remission. Quantitative real-time methylation-specific PCR was used to analyze the methylation status of the investigated genes. We observed that RA patients have lower levels of methylation of the FCER1G gene compared to controls, but we did not find any difference in the methylation status of this gene between patients with high disease activity and remission. The results of this study suggest that FCER1G gene methylation may be a new potential epigenetic marker of RA that is independent of disease activity. MDPI 2022-08-09 /pmc/articles/PMC9410058/ /pubmed/36012903 http://dx.doi.org/10.3390/jcm11164664 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Podgórska, Dominika
Cieśla, Marek
Kolarz, Bogdan
FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title_full FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title_fullStr FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title_full_unstemmed FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title_short FCER1G Gene Hypomethylation in Patients with Rheumatoid Arthritis
title_sort fcer1g gene hypomethylation in patients with rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410058/
https://www.ncbi.nlm.nih.gov/pubmed/36012903
http://dx.doi.org/10.3390/jcm11164664
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