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A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis

INTRODUCTION: The severity of joint damage progression in rheumatoid arthritis (RA) is heritable. Several genetic variants have been identified, but together explain only part of the total genetic effect. Variants in Interleukin-6 (IL-6), Interleukin-10 (IL-10), C5-TRAF1, and Fc-receptor-like-3 (FCR...

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Autores principales: van Steenbergen, Hanna W, Rodríguez-Rodríguez, Luis, Berglin, Ewa, Zhernakova, Alexandra, Knevel, Rachel, Ivorra-Cortés, Jose, Huizinga, Tom WJ, Fernández-Gutiérrez, Benjamin, Gregersen, Peter K, Rantapää-Dahlqvist, Solbritt, van der Helm-van Mil, Annette HM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318544/
https://www.ncbi.nlm.nih.gov/pubmed/25566937
http://dx.doi.org/10.1186/s13075-014-0514-0
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author van Steenbergen, Hanna W
Rodríguez-Rodríguez, Luis
Berglin, Ewa
Zhernakova, Alexandra
Knevel, Rachel
Ivorra-Cortés, Jose
Huizinga, Tom WJ
Fernández-Gutiérrez, Benjamin
Gregersen, Peter K
Rantapää-Dahlqvist, Solbritt
van der Helm-van Mil, Annette HM
author_facet van Steenbergen, Hanna W
Rodríguez-Rodríguez, Luis
Berglin, Ewa
Zhernakova, Alexandra
Knevel, Rachel
Ivorra-Cortés, Jose
Huizinga, Tom WJ
Fernández-Gutiérrez, Benjamin
Gregersen, Peter K
Rantapää-Dahlqvist, Solbritt
van der Helm-van Mil, Annette HM
author_sort van Steenbergen, Hanna W
collection PubMed
description INTRODUCTION: The severity of joint damage progression in rheumatoid arthritis (RA) is heritable. Several genetic variants have been identified, but together explain only part of the total genetic effect. Variants in Interleukin-6 (IL-6), Interleukin-10 (IL-10), C5-TRAF1, and Fc-receptor-like-3 (FCRL3) have been described to associate with radiographic progression, but results of different studies were incongruent. We aimed to clarify associations of these variants with radiographic progression by evaluating six independent cohorts. METHODS: In total 5,895 sets of radiographs of 2,493 RA-patients included in six different independent datasets from the Netherlands, Sweden, Spain and North-America were studied in relation to rs1800795 (IL-6), rs1800896 (IL-10), rs2900180 (C5-TRAF1) and rs7528684 (FCRL3). Associations were tested in the total RA-populations and in anti-citrullinated peptide antibodies (ACPA)-positive and ACPA-negative subgroups per cohort, followed by meta-analyses. Furthermore, the associated region C5-TRAF1 was fine-mapped in the ACPA-negative Dutch RA-patients. RESULTS: No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684 (FCRL3) in the total RA-population and after stratification for ACPA. Rs2900180 in C5-TRAF1 was associated with radiographic progression in the ACPA-negative population (P-value meta-analysis = 5.85 × 10(−7)); the minor allele was associated with more radiographic progression. Fine-mapping revealed a region of 66Kb that was associated; the lowest P-value was for rs7021880 in TRAF1. The P-value for rs7021880 in meta-analysis was 6.35 × 10(−8). Previous studies indicate that the region of rs7021880 was associated with RNA expression of TRAF1 and C5. CONCLUSION: Variants in IL-6, IL-10 and FCRL3 were not associated with radiographic progression. Rs2900180 in C5-TRAF1 and linked variants in a 66Kb region were associated with radiographic progression in ACPA-negative RA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0514-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-43185442015-02-06 A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis van Steenbergen, Hanna W Rodríguez-Rodríguez, Luis Berglin, Ewa Zhernakova, Alexandra Knevel, Rachel Ivorra-Cortés, Jose Huizinga, Tom WJ Fernández-Gutiérrez, Benjamin Gregersen, Peter K Rantapää-Dahlqvist, Solbritt van der Helm-van Mil, Annette HM Arthritis Res Ther Research Article INTRODUCTION: The severity of joint damage progression in rheumatoid arthritis (RA) is heritable. Several genetic variants have been identified, but together explain only part of the total genetic effect. Variants in Interleukin-6 (IL-6), Interleukin-10 (IL-10), C5-TRAF1, and Fc-receptor-like-3 (FCRL3) have been described to associate with radiographic progression, but results of different studies were incongruent. We aimed to clarify associations of these variants with radiographic progression by evaluating six independent cohorts. METHODS: In total 5,895 sets of radiographs of 2,493 RA-patients included in six different independent datasets from the Netherlands, Sweden, Spain and North-America were studied in relation to rs1800795 (IL-6), rs1800896 (IL-10), rs2900180 (C5-TRAF1) and rs7528684 (FCRL3). Associations were tested in the total RA-populations and in anti-citrullinated peptide antibodies (ACPA)-positive and ACPA-negative subgroups per cohort, followed by meta-analyses. Furthermore, the associated region C5-TRAF1 was fine-mapped in the ACPA-negative Dutch RA-patients. RESULTS: No associations were found for rs1800795 (IL-6), rs1800896 (IL-10) and rs7528684 (FCRL3) in the total RA-population and after stratification for ACPA. Rs2900180 in C5-TRAF1 was associated with radiographic progression in the ACPA-negative population (P-value meta-analysis = 5.85 × 10(−7)); the minor allele was associated with more radiographic progression. Fine-mapping revealed a region of 66Kb that was associated; the lowest P-value was for rs7021880 in TRAF1. The P-value for rs7021880 in meta-analysis was 6.35 × 10(−8). Previous studies indicate that the region of rs7021880 was associated with RNA expression of TRAF1 and C5. CONCLUSION: Variants in IL-6, IL-10 and FCRL3 were not associated with radiographic progression. Rs2900180 in C5-TRAF1 and linked variants in a 66Kb region were associated with radiographic progression in ACPA-negative RA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0514-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-08 2015 /pmc/articles/PMC4318544/ /pubmed/25566937 http://dx.doi.org/10.1186/s13075-014-0514-0 Text en © van Steenbergen et al.; licensee BioMed Central. 2015 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 work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
van Steenbergen, Hanna W
Rodríguez-Rodríguez, Luis
Berglin, Ewa
Zhernakova, Alexandra
Knevel, Rachel
Ivorra-Cortés, Jose
Huizinga, Tom WJ
Fernández-Gutiérrez, Benjamin
Gregersen, Peter K
Rantapää-Dahlqvist, Solbritt
van der Helm-van Mil, Annette HM
A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title_full A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title_fullStr A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title_full_unstemmed A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title_short A genetic study on C5-TRAF1 and progression of joint damage in rheumatoid arthritis
title_sort genetic study on c5-traf1 and progression of joint damage in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318544/
https://www.ncbi.nlm.nih.gov/pubmed/25566937
http://dx.doi.org/10.1186/s13075-014-0514-0
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