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Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study
OBJECTIVE: Glutathione-S-transferases (GSTs) play an important role in tobacco smoke detoxification, interestingly approximately 50% of individuals in most human populations lack the gene GSTM1 due to copy number variation (CNV). We aimed to investigate GSTM1 CNV in Rheumatoid Arthritis (RA) in rela...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062563/ https://www.ncbi.nlm.nih.gov/pubmed/21445357 http://dx.doi.org/10.1371/journal.pone.0017880 |
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author | Lundström, Emeli Hartshorne, Toinette Li, Kelly Lindblad, Staffan Wick, Marius C. Bengtsson, Camilla Alfredsson, Lars Klareskog, Lars Padyukov, Leonid |
author_facet | Lundström, Emeli Hartshorne, Toinette Li, Kelly Lindblad, Staffan Wick, Marius C. Bengtsson, Camilla Alfredsson, Lars Klareskog, Lars Padyukov, Leonid |
author_sort | Lundström, Emeli |
collection | PubMed |
description | OBJECTIVE: Glutathione-S-transferases (GSTs) play an important role in tobacco smoke detoxification, interestingly approximately 50% of individuals in most human populations lack the gene GSTM1 due to copy number variation (CNV). We aimed to investigate GSTM1 CNV in Rheumatoid Arthritis (RA) in relation to smoking and HLA-DRB1 shared epitope; the two best known risk factors for RA and in addition, to perform subanalyses in patients where relations between variations in GSTM1 and RA have previously been described. METHODS: qPCR was performed using TaqMan Copy Number assays (Applied Biosystems) for 2426 incident RA cases and 1257 controls from the Swedish EIRA. Odds ratio (OR) together with 95% confidence intervals (CI) was calculated and used as a measure of the relative risk of developing RA. RESULTS: No association between RA and GSTM1 CNV was observed when analyzing whole EIRA. However, ≥1 copy of GSTM1 appears to be a significant risk factor for autoantibody positive RA in non-smoking females ≥60 years (OR: 2.00 95% CI: 1.07–3.74), a population where such relationships have previously been described. Our data further suggest a protective effect of GSTM1 in ACPA-negative smoking men (OR: 0.56 95% CI: 0.35–0.90). CONCLUSION: We assessed the exact number of GSTM1 gene copies in relation to development and severity of RA. Our data provide support for the notion that variations in copy numbers of GSTM1 may influence risk in certain subsets of RA, but do not support a role for GSTM1 CNV as a factor that more generally modifies the influence of smoking on RA. |
format | Text |
id | pubmed-3062563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30625632011-03-28 Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study Lundström, Emeli Hartshorne, Toinette Li, Kelly Lindblad, Staffan Wick, Marius C. Bengtsson, Camilla Alfredsson, Lars Klareskog, Lars Padyukov, Leonid PLoS One Research Article OBJECTIVE: Glutathione-S-transferases (GSTs) play an important role in tobacco smoke detoxification, interestingly approximately 50% of individuals in most human populations lack the gene GSTM1 due to copy number variation (CNV). We aimed to investigate GSTM1 CNV in Rheumatoid Arthritis (RA) in relation to smoking and HLA-DRB1 shared epitope; the two best known risk factors for RA and in addition, to perform subanalyses in patients where relations between variations in GSTM1 and RA have previously been described. METHODS: qPCR was performed using TaqMan Copy Number assays (Applied Biosystems) for 2426 incident RA cases and 1257 controls from the Swedish EIRA. Odds ratio (OR) together with 95% confidence intervals (CI) was calculated and used as a measure of the relative risk of developing RA. RESULTS: No association between RA and GSTM1 CNV was observed when analyzing whole EIRA. However, ≥1 copy of GSTM1 appears to be a significant risk factor for autoantibody positive RA in non-smoking females ≥60 years (OR: 2.00 95% CI: 1.07–3.74), a population where such relationships have previously been described. Our data further suggest a protective effect of GSTM1 in ACPA-negative smoking men (OR: 0.56 95% CI: 0.35–0.90). CONCLUSION: We assessed the exact number of GSTM1 gene copies in relation to development and severity of RA. Our data provide support for the notion that variations in copy numbers of GSTM1 may influence risk in certain subsets of RA, but do not support a role for GSTM1 CNV as a factor that more generally modifies the influence of smoking on RA. Public Library of Science 2011-03-22 /pmc/articles/PMC3062563/ /pubmed/21445357 http://dx.doi.org/10.1371/journal.pone.0017880 Text en Lundström et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lundström, Emeli Hartshorne, Toinette Li, Kelly Lindblad, Staffan Wick, Marius C. Bengtsson, Camilla Alfredsson, Lars Klareskog, Lars Padyukov, Leonid Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title | Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title_full | Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title_fullStr | Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title_full_unstemmed | Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title_short | Effects of GSTM1 in Rheumatoid Arthritis; Results from the Swedish EIRA study |
title_sort | effects of gstm1 in rheumatoid arthritis; results from the swedish eira study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062563/ https://www.ncbi.nlm.nih.gov/pubmed/21445357 http://dx.doi.org/10.1371/journal.pone.0017880 |
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