Cargando…
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
Mouth ulcers are the most common ulcerative condition and encompass several clinical diagnoses, including recurrent aphthous stomatitis (RAS). Despite previous evidence for heritability, it is not clear which specific genetic loci are implicated in RAS. In this genome-wide association study (n = 461...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400940/ https://www.ncbi.nlm.nih.gov/pubmed/30837455 http://dx.doi.org/10.1038/s41467-019-08923-6 |
_version_ | 1783400050384175104 |
---|---|
author | Dudding, Tom Haworth, Simon Lind, Penelope A. Sathirapongsasuti, J. Fah Tung, Joyce Y. Mitchell, Ruth Colodro-Conde, Lucía Medland, Sarah E. Gordon, Scott Elsworth, Benjamin Paternoster, Lavinia Franks, Paul W. Thomas, Steven J. Martin, Nicholas G. Timpson, Nicholas J. |
author_facet | Dudding, Tom Haworth, Simon Lind, Penelope A. Sathirapongsasuti, J. Fah Tung, Joyce Y. Mitchell, Ruth Colodro-Conde, Lucía Medland, Sarah E. Gordon, Scott Elsworth, Benjamin Paternoster, Lavinia Franks, Paul W. Thomas, Steven J. Martin, Nicholas G. Timpson, Nicholas J. |
author_sort | Dudding, Tom |
collection | PubMed |
description | Mouth ulcers are the most common ulcerative condition and encompass several clinical diagnoses, including recurrent aphthous stomatitis (RAS). Despite previous evidence for heritability, it is not clear which specific genetic loci are implicated in RAS. In this genome-wide association study (n = 461,106) heritability is estimated at 8.2% (95% CI: 6.4%, 9.9%). This study finds 97 variants which alter the odds of developing non-specific mouth ulcers and replicate these in an independent cohort (n = 355,744) (lead variant after meta-analysis: rs76830965, near IL12A, OR 0.72 (95% CI: 0.71, 0.73); P = 4.4e−483). Additional effect estimates from three independent cohorts with more specific phenotyping and specific study characteristics support many of these findings. In silico functional analyses provide evidence for a role of T cell regulation in the aetiology of mouth ulcers. These results provide novel insight into the pathogenesis of a common, important condition. |
format | Online Article Text |
id | pubmed-6400940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64009402019-03-07 Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci Dudding, Tom Haworth, Simon Lind, Penelope A. Sathirapongsasuti, J. Fah Tung, Joyce Y. Mitchell, Ruth Colodro-Conde, Lucía Medland, Sarah E. Gordon, Scott Elsworth, Benjamin Paternoster, Lavinia Franks, Paul W. Thomas, Steven J. Martin, Nicholas G. Timpson, Nicholas J. Nat Commun Article Mouth ulcers are the most common ulcerative condition and encompass several clinical diagnoses, including recurrent aphthous stomatitis (RAS). Despite previous evidence for heritability, it is not clear which specific genetic loci are implicated in RAS. In this genome-wide association study (n = 461,106) heritability is estimated at 8.2% (95% CI: 6.4%, 9.9%). This study finds 97 variants which alter the odds of developing non-specific mouth ulcers and replicate these in an independent cohort (n = 355,744) (lead variant after meta-analysis: rs76830965, near IL12A, OR 0.72 (95% CI: 0.71, 0.73); P = 4.4e−483). Additional effect estimates from three independent cohorts with more specific phenotyping and specific study characteristics support many of these findings. In silico functional analyses provide evidence for a role of T cell regulation in the aetiology of mouth ulcers. These results provide novel insight into the pathogenesis of a common, important condition. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6400940/ /pubmed/30837455 http://dx.doi.org/10.1038/s41467-019-08923-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dudding, Tom Haworth, Simon Lind, Penelope A. Sathirapongsasuti, J. Fah Tung, Joyce Y. Mitchell, Ruth Colodro-Conde, Lucía Medland, Sarah E. Gordon, Scott Elsworth, Benjamin Paternoster, Lavinia Franks, Paul W. Thomas, Steven J. Martin, Nicholas G. Timpson, Nicholas J. Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title | Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title_full | Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title_fullStr | Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title_full_unstemmed | Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title_short | Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
title_sort | genome wide analysis for mouth ulcers identifies associations at immune regulatory loci |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400940/ https://www.ncbi.nlm.nih.gov/pubmed/30837455 http://dx.doi.org/10.1038/s41467-019-08923-6 |
work_keys_str_mv | AT duddingtom genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT haworthsimon genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT lindpenelopea genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT sathirapongsasutijfah genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT tungjoycey genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT mitchellruth genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT colodrocondelucia genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT medlandsarahe genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT gordonscott genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT elsworthbenjamin genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT paternosterlavinia genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT frankspaulw genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT thomasstevenj genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT martinnicholasg genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci AT timpsonnicholasj genomewideanalysisformouthulcersidentifiesassociationsatimmuneregulatoryloci |