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Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study
INTRODUCTION: A candidate gene approach, in a large case–control association study in the Dutch population, has shown that a 480 kb block on chromosome 4q27 encompassing KIAA1109/Tenr/IL2/IL21 genes is associated with rheumatoid arthritis. Compared with case–control association studies, family-based...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688193/ https://www.ncbi.nlm.nih.gov/pubmed/19302705 http://dx.doi.org/10.1186/ar2654 |
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author | Teixeira, Vitor Hugo Pierlot, Celine Migliorini, Paola Balsa, Alejandro Westhovens, René Barrera, Pilar Alves, Helena Vaz, Carlos Fernandes, Manuela Pascual-Salcedo, Dora Bombardieri, Stefano Dequeker, Jan Radstake, Timothy R Van Riel, Piet van de Putte, Leo Lopes-Vaz, Antonio Bardin, Thomas Prum, Bernard Cornélis, François Petit-Teixeira, Elisabeth |
author_facet | Teixeira, Vitor Hugo Pierlot, Celine Migliorini, Paola Balsa, Alejandro Westhovens, René Barrera, Pilar Alves, Helena Vaz, Carlos Fernandes, Manuela Pascual-Salcedo, Dora Bombardieri, Stefano Dequeker, Jan Radstake, Timothy R Van Riel, Piet van de Putte, Leo Lopes-Vaz, Antonio Bardin, Thomas Prum, Bernard Cornélis, François Petit-Teixeira, Elisabeth |
author_sort | Teixeira, Vitor Hugo |
collection | PubMed |
description | INTRODUCTION: A candidate gene approach, in a large case–control association study in the Dutch population, has shown that a 480 kb block on chromosome 4q27 encompassing KIAA1109/Tenr/IL2/IL21 genes is associated with rheumatoid arthritis. Compared with case–control association studies, family-based studies have the added advantage of controlling potential differences in population structure. Therefore, our aim was to test this association in populations of European origin by using a family-based approach. METHODS: A total of 1,302 West European white individuals from 434 trio families were genotyped for the rs4505848, rs11732095, rs6822844, rs4492018 and rs1398553 polymorphisms using the TaqMan Allelic discrimination assay (Applied Biosystems). The genetic association analyses for each SNP and haplotype were performed using the Transmission Disequilibrium Test and the genotype relative risk. RESULTS: We observed evidence for association of the heterozygous rs4505848-AG genotype with rheumatoid arthritis (P = 0.04); however, no significance was found after Bonferroni correction. In concordance with previous findings in the Dutch population, we observed a trend of undertransmission for the rs6822844-T allele and rs6822844-GT genotype to rheumatoid arthritis patients. We further investigated the five SNP haplotypes of the KIAA1109/Tenr/IL2/IL21 gene region. We observed, as described in the Dutch population, a nonsignificant undertransmission of the AATGG haplotype to rheumatoid arthritis patients. CONCLUSIONS: Using a family-based study, we have provided a trend for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in populations of European descent. Nevertheless, we failed to replicate a significant association of this region in our rheumatoid arthritis family sample. Further investigation of this region, including detection and testing of all variants, is required to confirm rheumatoid arthritis association. |
format | Text |
id | pubmed-2688193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26881932009-05-29 Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study Teixeira, Vitor Hugo Pierlot, Celine Migliorini, Paola Balsa, Alejandro Westhovens, René Barrera, Pilar Alves, Helena Vaz, Carlos Fernandes, Manuela Pascual-Salcedo, Dora Bombardieri, Stefano Dequeker, Jan Radstake, Timothy R Van Riel, Piet van de Putte, Leo Lopes-Vaz, Antonio Bardin, Thomas Prum, Bernard Cornélis, François Petit-Teixeira, Elisabeth Arthritis Res Ther Research Article INTRODUCTION: A candidate gene approach, in a large case–control association study in the Dutch population, has shown that a 480 kb block on chromosome 4q27 encompassing KIAA1109/Tenr/IL2/IL21 genes is associated with rheumatoid arthritis. Compared with case–control association studies, family-based studies have the added advantage of controlling potential differences in population structure. Therefore, our aim was to test this association in populations of European origin by using a family-based approach. METHODS: A total of 1,302 West European white individuals from 434 trio families were genotyped for the rs4505848, rs11732095, rs6822844, rs4492018 and rs1398553 polymorphisms using the TaqMan Allelic discrimination assay (Applied Biosystems). The genetic association analyses for each SNP and haplotype were performed using the Transmission Disequilibrium Test and the genotype relative risk. RESULTS: We observed evidence for association of the heterozygous rs4505848-AG genotype with rheumatoid arthritis (P = 0.04); however, no significance was found after Bonferroni correction. In concordance with previous findings in the Dutch population, we observed a trend of undertransmission for the rs6822844-T allele and rs6822844-GT genotype to rheumatoid arthritis patients. We further investigated the five SNP haplotypes of the KIAA1109/Tenr/IL2/IL21 gene region. We observed, as described in the Dutch population, a nonsignificant undertransmission of the AATGG haplotype to rheumatoid arthritis patients. CONCLUSIONS: Using a family-based study, we have provided a trend for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in populations of European descent. Nevertheless, we failed to replicate a significant association of this region in our rheumatoid arthritis family sample. Further investigation of this region, including detection and testing of all variants, is required to confirm rheumatoid arthritis association. BioMed Central 2009 2009-03-20 /pmc/articles/PMC2688193/ /pubmed/19302705 http://dx.doi.org/10.1186/ar2654 Text en Copyright © 2009 Teixeira et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Teixeira, Vitor Hugo Pierlot, Celine Migliorini, Paola Balsa, Alejandro Westhovens, René Barrera, Pilar Alves, Helena Vaz, Carlos Fernandes, Manuela Pascual-Salcedo, Dora Bombardieri, Stefano Dequeker, Jan Radstake, Timothy R Van Riel, Piet van de Putte, Leo Lopes-Vaz, Antonio Bardin, Thomas Prum, Bernard Cornélis, François Petit-Teixeira, Elisabeth Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title | Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title_full | Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title_fullStr | Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title_full_unstemmed | Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title_short | Testing for the association of the KIAA1109/Tenr/IL2/IL21 gene region with rheumatoid arthritis in a European family-based study |
title_sort | testing for the association of the kiaa1109/tenr/il2/il21 gene region with rheumatoid arthritis in a european family-based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688193/ https://www.ncbi.nlm.nih.gov/pubmed/19302705 http://dx.doi.org/10.1186/ar2654 |
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