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Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population

OBJECTIVE: Various cytokine polymorphisms have been associated with genetic risk factors predisposing to Rheumatoid Arthritis (RA) in different populations. To predict the clinical outcome as well as response to therapy in RA, studies aimed to describe genetic markers. The present study aims to sear...

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Autores principales: Yucel, Burcu, Sumer, Ceren, Gok, Ilhami, Karkucak, Murat, Alemdaroglu, Emel, Ucar, Fahri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754868/
https://www.ncbi.nlm.nih.gov/pubmed/33381695
http://dx.doi.org/10.14744/nci.2020.70845
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author Yucel, Burcu
Sumer, Ceren
Gok, Ilhami
Karkucak, Murat
Alemdaroglu, Emel
Ucar, Fahri
author_facet Yucel, Burcu
Sumer, Ceren
Gok, Ilhami
Karkucak, Murat
Alemdaroglu, Emel
Ucar, Fahri
author_sort Yucel, Burcu
collection PubMed
description OBJECTIVE: Various cytokine polymorphisms have been associated with genetic risk factors predisposing to Rheumatoid Arthritis (RA) in different populations. To predict the clinical outcome as well as response to therapy in RA, studies aimed to describe genetic markers. The present study aims to search for polymorphisms of 13 cytokine coding genes in the Eastern Black Sea Region of Turkey. METHODS: DNAs of 49 patients and 96 healthy bone marrow and kidney donors were isolated from peripheral blood samples. Genotyping was performed using the Heidelberg Cytokine Typing Tray kit. PCR products were visualized on an agarose gel, and results were analyzed using the interpretation scheme provided with the kit. Arlequin 3.5 software was used for statistical analysis. RESULTS: No positive association was found between allele frequencies and the disease. However, a negative association was found for the IL-A -889 C allele (p=0.02, OR=0.533, Wald’s 95% CI=0.318–0.893). IL-12 -1188 CC (p=0.01, OR=3.667, Wald’s 95% CI=1.246–10.786), IL-4 -1098 GT (p=0.02, OR=2.405, Wald’s 95% CI=1.129–5.125) genotypes were found positively associated with the RA, while IL-4 -590 CT (p=0.02, OR=0.422, Wald’s 95% CI=0.201–0.886) was found negatively associated with the disease. In addition, IL-6 GG haplotype was found positively associated with the RA (p=0.02, OR=1.880, Wald’s 95% CI=1.086–3.254). CONCLUSION: Our findings suggest that some polymorphisms of the IL-1A, IL-2, IL-4, IL-6 and IL-12 could be responsible for the susceptibility or protective to RA in our study population. Multi-centered and large numbers of subjects containing studies that search for cytokine polymorphisms will gather more information regarding the susceptibility to RA of Turkish patients.
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spelling pubmed-77548682020-12-29 Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population Yucel, Burcu Sumer, Ceren Gok, Ilhami Karkucak, Murat Alemdaroglu, Emel Ucar, Fahri North Clin Istanb Original Article OBJECTIVE: Various cytokine polymorphisms have been associated with genetic risk factors predisposing to Rheumatoid Arthritis (RA) in different populations. To predict the clinical outcome as well as response to therapy in RA, studies aimed to describe genetic markers. The present study aims to search for polymorphisms of 13 cytokine coding genes in the Eastern Black Sea Region of Turkey. METHODS: DNAs of 49 patients and 96 healthy bone marrow and kidney donors were isolated from peripheral blood samples. Genotyping was performed using the Heidelberg Cytokine Typing Tray kit. PCR products were visualized on an agarose gel, and results were analyzed using the interpretation scheme provided with the kit. Arlequin 3.5 software was used for statistical analysis. RESULTS: No positive association was found between allele frequencies and the disease. However, a negative association was found for the IL-A -889 C allele (p=0.02, OR=0.533, Wald’s 95% CI=0.318–0.893). IL-12 -1188 CC (p=0.01, OR=3.667, Wald’s 95% CI=1.246–10.786), IL-4 -1098 GT (p=0.02, OR=2.405, Wald’s 95% CI=1.129–5.125) genotypes were found positively associated with the RA, while IL-4 -590 CT (p=0.02, OR=0.422, Wald’s 95% CI=0.201–0.886) was found negatively associated with the disease. In addition, IL-6 GG haplotype was found positively associated with the RA (p=0.02, OR=1.880, Wald’s 95% CI=1.086–3.254). CONCLUSION: Our findings suggest that some polymorphisms of the IL-1A, IL-2, IL-4, IL-6 and IL-12 could be responsible for the susceptibility or protective to RA in our study population. Multi-centered and large numbers of subjects containing studies that search for cytokine polymorphisms will gather more information regarding the susceptibility to RA of Turkish patients. Kare Publishing 2020-11-11 /pmc/articles/PMC7754868/ /pubmed/33381695 http://dx.doi.org/10.14744/nci.2020.70845 Text en Copyright: © 2020 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Original Article
Yucel, Burcu
Sumer, Ceren
Gok, Ilhami
Karkucak, Murat
Alemdaroglu, Emel
Ucar, Fahri
Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title_full Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title_fullStr Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title_full_unstemmed Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title_short Associations between cytokine gene polymorphisms and rheumatoid arthritis in Turkish population
title_sort associations between cytokine gene polymorphisms and rheumatoid arthritis in turkish population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754868/
https://www.ncbi.nlm.nih.gov/pubmed/33381695
http://dx.doi.org/10.14744/nci.2020.70845
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