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Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease
Although dietary gluten is the trigger, celiac disease risk is strongly influenced by genetic variation in the major histocompatibility complex (MHC) region. We fine-mapped the MHC association signal to identify additional risk factors independent of the HLA-DQ alleles and observed five novel associ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449296/ https://www.ncbi.nlm.nih.gov/pubmed/25894500 http://dx.doi.org/10.1038/ng.3268 |
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author | Gutierrez-Achury, Javier Zhernakova, Alexandra Pulit, Sara L. Trynka, Gosia Hunt, Karen A. Romanos, Jihane Raychaudhuri, Soumya van Heel, David A. Wijmenga, Cisca de Bakker, Paul I.W. |
author_facet | Gutierrez-Achury, Javier Zhernakova, Alexandra Pulit, Sara L. Trynka, Gosia Hunt, Karen A. Romanos, Jihane Raychaudhuri, Soumya van Heel, David A. Wijmenga, Cisca de Bakker, Paul I.W. |
author_sort | Gutierrez-Achury, Javier |
collection | PubMed |
description | Although dietary gluten is the trigger, celiac disease risk is strongly influenced by genetic variation in the major histocompatibility complex (MHC) region. We fine-mapped the MHC association signal to identify additional risk factors independent of the HLA-DQ alleles and observed five novel associations that account for 18% of the genetic risk. Together with the 57 known non-MHC loci, genetic variation can now explain up to 48% of celiac disease heritability. |
format | Online Article Text |
id | pubmed-4449296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-44492962015-12-01 Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease Gutierrez-Achury, Javier Zhernakova, Alexandra Pulit, Sara L. Trynka, Gosia Hunt, Karen A. Romanos, Jihane Raychaudhuri, Soumya van Heel, David A. Wijmenga, Cisca de Bakker, Paul I.W. Nat Genet Article Although dietary gluten is the trigger, celiac disease risk is strongly influenced by genetic variation in the major histocompatibility complex (MHC) region. We fine-mapped the MHC association signal to identify additional risk factors independent of the HLA-DQ alleles and observed five novel associations that account for 18% of the genetic risk. Together with the 57 known non-MHC loci, genetic variation can now explain up to 48% of celiac disease heritability. 2015-04-20 2015-06 /pmc/articles/PMC4449296/ /pubmed/25894500 http://dx.doi.org/10.1038/ng.3268 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Gutierrez-Achury, Javier Zhernakova, Alexandra Pulit, Sara L. Trynka, Gosia Hunt, Karen A. Romanos, Jihane Raychaudhuri, Soumya van Heel, David A. Wijmenga, Cisca de Bakker, Paul I.W. Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title | Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title_full | Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title_fullStr | Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title_full_unstemmed | Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title_short | Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease |
title_sort | fine-mapping in the mhc region accounts for 18% additional genetic risk for celiac disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449296/ https://www.ncbi.nlm.nih.gov/pubmed/25894500 http://dx.doi.org/10.1038/ng.3268 |
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