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CD209 in inflammatory bowel disease: a case-control study in the Spanish population
BACKGROUND: The etiology of Ulcerative Colitis (UC) and Crohn's Disease (CD), considered together as Inflammatory Bowel Diseases (IBD), involves environmental and genetic factors. Although some genes are already known, the genetics underlying these diseases is complex and new candidates are con...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241584/ https://www.ncbi.nlm.nih.gov/pubmed/18070336 http://dx.doi.org/10.1186/1471-2350-8-75 |
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author | Núñez, Concepción Oliver, Javier Mendoza, Juan Luis Gómez-García, María Taxonera, Carlos Gómez, Luis M López-Nevot, Miguel A de la Concha, Emilio G Urcelay, Elena Martínez, Alfonso Martín, Javier |
author_facet | Núñez, Concepción Oliver, Javier Mendoza, Juan Luis Gómez-García, María Taxonera, Carlos Gómez, Luis M López-Nevot, Miguel A de la Concha, Emilio G Urcelay, Elena Martínez, Alfonso Martín, Javier |
author_sort | Núñez, Concepción |
collection | PubMed |
description | BACKGROUND: The etiology of Ulcerative Colitis (UC) and Crohn's Disease (CD), considered together as Inflammatory Bowel Diseases (IBD), involves environmental and genetic factors. Although some genes are already known, the genetics underlying these diseases is complex and new candidates are continuously emerging. The CD209 gene is located in a region linked previously to IBD and a CD209 functional polymorphism (rs4804803) has been associated to other inflammatory conditions. Our aim was to study the potential involvement of this CD209 variant in IBD susceptibility. METHODS: We performed a case-control study with 515 CD patients, 497 UC patients and 731 healthy controls, all of them white Spaniards. Samples were typed for the CD209 single nucleotide polymorphism (SNP) rs4804803 by TaqMan technology. Frequency comparisons were performed using χ(2 )tests. RESULTS: No association between CD209 and UC or CD was observed initially. However, stratification of UC patients by HLA-DR3 status, a strong protective allele, showed that carriage of the CD209_G allele could increase susceptibility in the subgroup of HLA-DR3-positive individuals (p = 0.03 OR = 1.77 95% CI 1.04–3.02, vs. controls). CONCLUSION: A functional variant in the CD209 gene, rs4804803, does not seem to be influencing Crohn's disease susceptibility. However, it could be involved in the etiology or pathology of Ulcerative Colitis in HLA-DR3-positive individuals but further studies are necessary. |
format | Text |
id | pubmed-2241584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22415842008-02-13 CD209 in inflammatory bowel disease: a case-control study in the Spanish population Núñez, Concepción Oliver, Javier Mendoza, Juan Luis Gómez-García, María Taxonera, Carlos Gómez, Luis M López-Nevot, Miguel A de la Concha, Emilio G Urcelay, Elena Martínez, Alfonso Martín, Javier BMC Med Genet Research Article BACKGROUND: The etiology of Ulcerative Colitis (UC) and Crohn's Disease (CD), considered together as Inflammatory Bowel Diseases (IBD), involves environmental and genetic factors. Although some genes are already known, the genetics underlying these diseases is complex and new candidates are continuously emerging. The CD209 gene is located in a region linked previously to IBD and a CD209 functional polymorphism (rs4804803) has been associated to other inflammatory conditions. Our aim was to study the potential involvement of this CD209 variant in IBD susceptibility. METHODS: We performed a case-control study with 515 CD patients, 497 UC patients and 731 healthy controls, all of them white Spaniards. Samples were typed for the CD209 single nucleotide polymorphism (SNP) rs4804803 by TaqMan technology. Frequency comparisons were performed using χ(2 )tests. RESULTS: No association between CD209 and UC or CD was observed initially. However, stratification of UC patients by HLA-DR3 status, a strong protective allele, showed that carriage of the CD209_G allele could increase susceptibility in the subgroup of HLA-DR3-positive individuals (p = 0.03 OR = 1.77 95% CI 1.04–3.02, vs. controls). CONCLUSION: A functional variant in the CD209 gene, rs4804803, does not seem to be influencing Crohn's disease susceptibility. However, it could be involved in the etiology or pathology of Ulcerative Colitis in HLA-DR3-positive individuals but further studies are necessary. BioMed Central 2007-12-10 /pmc/articles/PMC2241584/ /pubmed/18070336 http://dx.doi.org/10.1186/1471-2350-8-75 Text en Copyright © 2007 Núñez 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 Núñez, Concepción Oliver, Javier Mendoza, Juan Luis Gómez-García, María Taxonera, Carlos Gómez, Luis M López-Nevot, Miguel A de la Concha, Emilio G Urcelay, Elena Martínez, Alfonso Martín, Javier CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title | CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title_full | CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title_fullStr | CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title_full_unstemmed | CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title_short | CD209 in inflammatory bowel disease: a case-control study in the Spanish population |
title_sort | cd209 in inflammatory bowel disease: a case-control study in the spanish population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241584/ https://www.ncbi.nlm.nih.gov/pubmed/18070336 http://dx.doi.org/10.1186/1471-2350-8-75 |
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