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

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

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BORIS DOI
10.48350/158979
Date of Publication
February 5, 2021
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Department for BioMed...

Universitätsklinik fü...

Contributor
Ledergerber, Martina
Lang, Brian M
Heinrich, Henriette
Biedermann, Luc
Begré, Stefan
Department for BioMedical Research, Forschungsgruppe Neurologie
Zeitz, Jonas
Krupka, Niklasorcid-logo
Universitätsklinik für Viszerale Chirurgie und Medizin
Rickenbacher, Andreas
Turina, Matthias
Greuter, Thomas
Schreiner, Philipp
Roth, René
Siebenhüner, Alexander
Vavricka, Stephan R
Rogler, Gerhard
Beerenwinkel, Niko
Misselwitz, Benjamin
Universitätsklinik für Viszerale Chirurgie und Medizin, Viszeral- und Transplantationschirurgie
Universitätsklinik für Viszerale Chirurgie und Medizin, Gastroenterologie
Subject(s)

600 - Technology::610...

Series
BMC gastroenterology
ISSN or ISBN (if monograph)
1471-230X
Publisher
BioMed Central
Language
English
Publisher DOI
10.1186/s12876-021-01622-x
PubMed ID
33546600
Uncontrolled Keywords

Abdominal pain Crohn’...

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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/45752
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12876_2021_Article_1622.pdfAdobe PDF1.15 MBpublishedOpen
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