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Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis

BACKGROUND: Two novel genetic polymorphisms on chromosome 6q23 are associated with susceptibility to rheumatoid arthritis (RA). Both polymorphisms (rs6920220 and rs10499194) reside in a region close to the gene encoding tumour necrosis factor α-induced protein 3 (TNFAIP3). TNFAIP3 is a negative regu...

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Autores principales: Scherer, Hans Ulrich, van der Linden, Michael P M, Kurreeman, Fina A S, Stoeken-Rijsbergen, Gerrie, le Cessie, Saskia, Huizinga, Tom W J, van der Helm-van Mil, Annette H, Toes, René E M
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927680/
https://www.ncbi.nlm.nih.gov/pubmed/19366996
http://dx.doi.org/10.1136/ard.2008.106161
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author Scherer, Hans Ulrich
van der Linden, Michael P M
Kurreeman, Fina A S
Stoeken-Rijsbergen, Gerrie
le Cessie, Saskia
Huizinga, Tom W J
van der Helm-van Mil, Annette H
Toes, René E M
author_facet Scherer, Hans Ulrich
van der Linden, Michael P M
Kurreeman, Fina A S
Stoeken-Rijsbergen, Gerrie
le Cessie, Saskia
Huizinga, Tom W J
van der Helm-van Mil, Annette H
Toes, René E M
author_sort Scherer, Hans Ulrich
collection PubMed
description BACKGROUND: Two novel genetic polymorphisms on chromosome 6q23 are associated with susceptibility to rheumatoid arthritis (RA). Both polymorphisms (rs6920220 and rs10499194) reside in a region close to the gene encoding tumour necrosis factor α-induced protein 3 (TNFAIP3). TNFAIP3 is a negative regulator of NF-κB and is involved in inhibiting TNF-receptor-mediated signalling effects. Interestingly, the initial associations were detected in patients with longstanding RA. However, no association was found for rs10499194 in a Swedish cohort with early arthritis. This might be caused by over-representation of patients with severe disease in cohorts with longstanding RA. OBJECTIVE: To analyse the effect of the 6q23 region on the rate of joint destruction. METHODS: Five single nucleotide polymorphisms in 6q23 were genotyped in 324 Dutch patients with early RA. Genotypes were correlated with progression of radiographic joint damage for a follow-up time of 5 years. RESULTS: Two polymorphisms (rs675520 and rs9376293) were associated with severity of radiographic joint damage in patients positive for anti-citrullinated protein/peptide antibodies (ACPA). Importantly, the effects were present after correction for confounding factors such as secular trends in treatment. CONCLUSIONS: These data associate the 6q23 region with the rate of joint destruction in ACPA+ RA.
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spelling pubmed-29276802010-08-25 Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis Scherer, Hans Ulrich van der Linden, Michael P M Kurreeman, Fina A S Stoeken-Rijsbergen, Gerrie le Cessie, Saskia Huizinga, Tom W J van der Helm-van Mil, Annette H Toes, René E M Ann Rheum Dis Clinical and Epidemiological Research BACKGROUND: Two novel genetic polymorphisms on chromosome 6q23 are associated with susceptibility to rheumatoid arthritis (RA). Both polymorphisms (rs6920220 and rs10499194) reside in a region close to the gene encoding tumour necrosis factor α-induced protein 3 (TNFAIP3). TNFAIP3 is a negative regulator of NF-κB and is involved in inhibiting TNF-receptor-mediated signalling effects. Interestingly, the initial associations were detected in patients with longstanding RA. However, no association was found for rs10499194 in a Swedish cohort with early arthritis. This might be caused by over-representation of patients with severe disease in cohorts with longstanding RA. OBJECTIVE: To analyse the effect of the 6q23 region on the rate of joint destruction. METHODS: Five single nucleotide polymorphisms in 6q23 were genotyped in 324 Dutch patients with early RA. Genotypes were correlated with progression of radiographic joint damage for a follow-up time of 5 years. RESULTS: Two polymorphisms (rs675520 and rs9376293) were associated with severity of radiographic joint damage in patients positive for anti-citrullinated protein/peptide antibodies (ACPA). Importantly, the effects were present after correction for confounding factors such as secular trends in treatment. CONCLUSIONS: These data associate the 6q23 region with the rate of joint destruction in ACPA+ RA. BMJ Group 2009-04-14 /pmc/articles/PMC2927680/ /pubmed/19366996 http://dx.doi.org/10.1136/ard.2008.106161 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Clinical and Epidemiological Research
Scherer, Hans Ulrich
van der Linden, Michael P M
Kurreeman, Fina A S
Stoeken-Rijsbergen, Gerrie
le Cessie, Saskia
Huizinga, Tom W J
van der Helm-van Mil, Annette H
Toes, René E M
Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title_full Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title_fullStr Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title_full_unstemmed Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title_short Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
title_sort association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis
topic Clinical and Epidemiological Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927680/
https://www.ncbi.nlm.nih.gov/pubmed/19366996
http://dx.doi.org/10.1136/ard.2008.106161
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