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Genetic association and differential expression of PITX2 with acute appendicitis
Appendicitis affects 9% of Americans and is the most common diagnosis requiring hospitalization of both children and adults. We performed a genome-wide association study of self-reported appendectomy with 18,773 affected adults and 114,907 unaffected adults of European American ancestry. A significa...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514078/ https://www.ncbi.nlm.nih.gov/pubmed/30392061 http://dx.doi.org/10.1007/s00439-018-1956-2 |
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author | Orlova, Ekaterina Yeh, Andrew Shi, Min Firek, Brian Ranganathan, Sarangarajan Whitcomb, David C. Finegold, David N. Ferrell, Robert E. Barmada, M. Michael Marazita, Mary L. Hinds, David A. Shaffer, John R. Morowitz, Michael J. |
author_facet | Orlova, Ekaterina Yeh, Andrew Shi, Min Firek, Brian Ranganathan, Sarangarajan Whitcomb, David C. Finegold, David N. Ferrell, Robert E. Barmada, M. Michael Marazita, Mary L. Hinds, David A. Shaffer, John R. Morowitz, Michael J. |
author_sort | Orlova, Ekaterina |
collection | PubMed |
description | Appendicitis affects 9% of Americans and is the most common diagnosis requiring hospitalization of both children and adults. We performed a genome-wide association study of self-reported appendectomy with 18,773 affected adults and 114,907 unaffected adults of European American ancestry. A significant association with appendectomy was observed at 4q25 near the gene PITX2 (rs2129979, p value = 8.82 × 10(−14)) and was replicated in an independent sample of Caucasians (59 affected, 607 unaffected; p value = 0.005). Meta-analysis of the associated variant across our two cohorts and cohorts from Iceland and the Netherlands (in which this association had previously been reported) showed strong cumulative evidence of association (OR = 1.12; 95% CI 1.09–1.14; p value = 1.81 × 10(−23)) and some evidence for effect heterogeneity (p value = 0.03). Eight other loci were identified at suggestive significance in the discovery GWAS. Associations were followed up by measuring gene expression across resected appendices with varying levels of inflammation (N = 75). We measured expression of 27 genes based on physical proximity to the GWAS signals, evidence of being targeted by eQTLs near the signals according to RegulomeDB (score = 1), or both. Four of the 27 genes (including PITX2) showed significant evidence (p values < 0.0033) of differential expression across categories of appendix inflammation. An additional ten genes showed nominal evidence (p value < 0.05) of differential expression, which, together with the significant genes, is more than expected by chance (p value = 6.6 × 10(−12)). PITX2 impacts morphological development of intestinal tissue, promotes an anti-oxidant response, and its expression correlates with levels of intestinal bacteria and colonic inflammation. Further studies of the role of PITX2 in appendicitis are warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00439-018-1956-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6514078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-65140782019-05-28 Genetic association and differential expression of PITX2 with acute appendicitis Orlova, Ekaterina Yeh, Andrew Shi, Min Firek, Brian Ranganathan, Sarangarajan Whitcomb, David C. Finegold, David N. Ferrell, Robert E. Barmada, M. Michael Marazita, Mary L. Hinds, David A. Shaffer, John R. Morowitz, Michael J. Hum Genet Original Investigation Appendicitis affects 9% of Americans and is the most common diagnosis requiring hospitalization of both children and adults. We performed a genome-wide association study of self-reported appendectomy with 18,773 affected adults and 114,907 unaffected adults of European American ancestry. A significant association with appendectomy was observed at 4q25 near the gene PITX2 (rs2129979, p value = 8.82 × 10(−14)) and was replicated in an independent sample of Caucasians (59 affected, 607 unaffected; p value = 0.005). Meta-analysis of the associated variant across our two cohorts and cohorts from Iceland and the Netherlands (in which this association had previously been reported) showed strong cumulative evidence of association (OR = 1.12; 95% CI 1.09–1.14; p value = 1.81 × 10(−23)) and some evidence for effect heterogeneity (p value = 0.03). Eight other loci were identified at suggestive significance in the discovery GWAS. Associations were followed up by measuring gene expression across resected appendices with varying levels of inflammation (N = 75). We measured expression of 27 genes based on physical proximity to the GWAS signals, evidence of being targeted by eQTLs near the signals according to RegulomeDB (score = 1), or both. Four of the 27 genes (including PITX2) showed significant evidence (p values < 0.0033) of differential expression across categories of appendix inflammation. An additional ten genes showed nominal evidence (p value < 0.05) of differential expression, which, together with the significant genes, is more than expected by chance (p value = 6.6 × 10(−12)). PITX2 impacts morphological development of intestinal tissue, promotes an anti-oxidant response, and its expression correlates with levels of intestinal bacteria and colonic inflammation. Further studies of the role of PITX2 in appendicitis are warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00439-018-1956-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-11-03 2019 /pmc/articles/PMC6514078/ /pubmed/30392061 http://dx.doi.org/10.1007/s00439-018-1956-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Investigation Orlova, Ekaterina Yeh, Andrew Shi, Min Firek, Brian Ranganathan, Sarangarajan Whitcomb, David C. Finegold, David N. Ferrell, Robert E. Barmada, M. Michael Marazita, Mary L. Hinds, David A. Shaffer, John R. Morowitz, Michael J. Genetic association and differential expression of PITX2 with acute appendicitis |
title | Genetic association and differential expression of PITX2 with acute appendicitis |
title_full | Genetic association and differential expression of PITX2 with acute appendicitis |
title_fullStr | Genetic association and differential expression of PITX2 with acute appendicitis |
title_full_unstemmed | Genetic association and differential expression of PITX2 with acute appendicitis |
title_short | Genetic association and differential expression of PITX2 with acute appendicitis |
title_sort | genetic association and differential expression of pitx2 with acute appendicitis |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514078/ https://www.ncbi.nlm.nih.gov/pubmed/30392061 http://dx.doi.org/10.1007/s00439-018-1956-2 |
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