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Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management

BACKGROUND: Abdominal pain is a frequent symptom in patients with inflammatory bowel disease (IBD) including Crohn’s disease (CD) and ulcerative colitis (UC). Pain can result from ongoing inflammation or functional disorders imitating irritable bowel syndrome (IBS). Several single-nucleotide polymor...

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Autores principales: Ledergerber, Martina, Lang, Brian M., Heinrich, Henriette, Biedermann, Luc, Begré, Stefan, Zeitz, Jonas, Krupka, Niklas, Rickenbacher, Andreas, Turina, Matthias, Greuter, Thomas, Schreiner, Philipp, Roth, René, Siebenhüner, Alexander, Vavricka, Stephan R., Rogler, Gerhard, Beerenwinkel, Niko, Misselwitz, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866750/
https://www.ncbi.nlm.nih.gov/pubmed/33546600
http://dx.doi.org/10.1186/s12876-021-01622-x
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author Ledergerber, Martina
Lang, Brian M.
Heinrich, Henriette
Biedermann, Luc
Begré, Stefan
Zeitz, Jonas
Krupka, Niklas
Rickenbacher, Andreas
Turina, Matthias
Greuter, Thomas
Schreiner, Philipp
Roth, René
Siebenhüner, Alexander
Vavricka, Stephan R.
Rogler, Gerhard
Beerenwinkel, Niko
Misselwitz, Benjamin
author_facet Ledergerber, Martina
Lang, Brian M.
Heinrich, Henriette
Biedermann, Luc
Begré, Stefan
Zeitz, Jonas
Krupka, Niklas
Rickenbacher, Andreas
Turina, Matthias
Greuter, Thomas
Schreiner, Philipp
Roth, René
Siebenhüner, Alexander
Vavricka, Stephan R.
Rogler, Gerhard
Beerenwinkel, Niko
Misselwitz, Benjamin
author_sort Ledergerber, Martina
collection PubMed
description BACKGROUND: Abdominal pain is a frequent symptom in patients with inflammatory bowel disease (IBD) including Crohn’s disease (CD) and ulcerative colitis (UC). Pain can result from ongoing inflammation or functional disorders imitating irritable bowel syndrome (IBS). Several single-nucleotide polymorphisms (SNPs) have been associated with IBS. However, the impact of IBS genetics on the clinical course of IBD, especially pain levels of patients remains unclear. METHODS: Data of 857 UC and 1206 CD patients from the Swiss IBD Cohort Study were analysed. We tested the association of the maximum of the abdominal pain item of disease activity indices in UC and CD over the study period with 16 IBS-associated SNPs, using multivariate ANOVA models. RESULTS: In UC patients, the SNPs rs1042713 (located on the ADRB2 gene) and rs4663866 (close to the HES6 gene) were associated with higher abdominal pain levels (P = 0.044; P = 0.037, respectively). Abdominal pain was not associated with any markers of patient management in a model adjusted for confounders. In CD patients, higher levels of abdominal pain correlated with the number of physician contacts (P < 10(–15)), examinations (P < 10(–12)), medical therapies (P = 0.023) and weeks of hospitalisation (P = 0.0013) in a multivariate model. CONCLUSIONS: We detected an association between maximal abdominal pain in UC patients and two IBS-associated SNPs. Abdominal pain levels had a pronounced impact on diagnostic and therapeutic procedures in CD but not in UC patients.
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spelling pubmed-78667502021-02-08 Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management Ledergerber, Martina Lang, Brian M. Heinrich, Henriette Biedermann, Luc Begré, Stefan Zeitz, Jonas Krupka, Niklas Rickenbacher, Andreas Turina, Matthias Greuter, Thomas Schreiner, Philipp Roth, René Siebenhüner, Alexander Vavricka, Stephan R. Rogler, Gerhard Beerenwinkel, Niko Misselwitz, Benjamin BMC Gastroenterol Research Article BACKGROUND: Abdominal pain is a frequent symptom in patients with inflammatory bowel disease (IBD) including Crohn’s disease (CD) and ulcerative colitis (UC). Pain can result from ongoing inflammation or functional disorders imitating irritable bowel syndrome (IBS). Several single-nucleotide polymorphisms (SNPs) have been associated with IBS. However, the impact of IBS genetics on the clinical course of IBD, especially pain levels of patients remains unclear. METHODS: Data of 857 UC and 1206 CD patients from the Swiss IBD Cohort Study were analysed. We tested the association of the maximum of the abdominal pain item of disease activity indices in UC and CD over the study period with 16 IBS-associated SNPs, using multivariate ANOVA models. RESULTS: In UC patients, the SNPs rs1042713 (located on the ADRB2 gene) and rs4663866 (close to the HES6 gene) were associated with higher abdominal pain levels (P = 0.044; P = 0.037, respectively). Abdominal pain was not associated with any markers of patient management in a model adjusted for confounders. In CD patients, higher levels of abdominal pain correlated with the number of physician contacts (P < 10(–15)), examinations (P < 10(–12)), medical therapies (P = 0.023) and weeks of hospitalisation (P = 0.0013) in a multivariate model. CONCLUSIONS: We detected an association between maximal abdominal pain in UC patients and two IBS-associated SNPs. Abdominal pain levels had a pronounced impact on diagnostic and therapeutic procedures in CD but not in UC patients. BioMed Central 2021-02-05 /pmc/articles/PMC7866750/ /pubmed/33546600 http://dx.doi.org/10.1186/s12876-021-01622-x Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Ledergerber, Martina
Lang, Brian M.
Heinrich, Henriette
Biedermann, Luc
Begré, Stefan
Zeitz, Jonas
Krupka, Niklas
Rickenbacher, Andreas
Turina, Matthias
Greuter, Thomas
Schreiner, Philipp
Roth, René
Siebenhüner, Alexander
Vavricka, Stephan R.
Rogler, Gerhard
Beerenwinkel, Niko
Misselwitz, Benjamin
Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title_full Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title_fullStr Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title_full_unstemmed Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title_short Abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
title_sort abdominal pain in patients with inflammatory bowel disease: association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866750/
https://www.ncbi.nlm.nih.gov/pubmed/33546600
http://dx.doi.org/10.1186/s12876-021-01622-x
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