TY - JOUR
T1 - Abdominal pain in patients with inflammatory bowel disease
T2 - association with single-nucleotide polymorphisms prevalent in irritable bowel syndrome and clinical management
AU - the Swiss IBD Cohort Study Group
AU - Ledergerber, Martina
AU - Lang, Brian M.
AU - Heinrich, Henriette
AU - Biedermann, Luc
AU - Begré, Stefan
AU - Zeitz, Jonas
AU - Krupka, Niklas
AU - Rickenbacher, Andreas
AU - Turina, Matthias
AU - Greuter, Thomas
AU - Schreiner, Philipp
AU - Roth, René
AU - Siebenhüner, Alexander
AU - Vavricka, Stephan R.
AU - Rogler, Gerhard
AU - Beerenwinkel, Niko
AU - Misselwitz, Benjamin
AU - Anderegg, Claudia
AU - Bauerfeind, Peter
AU - Beglinger, Christoph
AU - Belli, Dominique
AU - Bengoa, José M.
AU - Bigler, Beat
AU - Binek, Janek
AU - Blattmann, Mirjam
AU - Boehm, Stephan
AU - Borovicka, Jan
AU - Braegger, Christian P.
AU - Brunner, Nora
AU - Bühr, Patrick
AU - Burnand, Bernard
AU - Burri, Emanuel
AU - Buyse, Sophie
AU - Cremer, Matthias
AU - Criblez, Dominique H.
AU - de Saussure, Philippe
AU - Degen, Lukas
AU - Delarive, Joakim
AU - Doerig, Christopher
AU - Dora, Barbara
AU - Dorta, Gian
AU - Egger, Mara
AU - Ehmann, Tobias
AU - El-Wafa, Ali
AU - Engelmann, Matthias
AU - Ezri, Jessica
AU - Felley, Christian
AU - Fliegner, Markus
AU - Fournier, Nicolas
AU - Sauter, Bernhard
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - 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.
AB - 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.
KW - Abdominal pain
KW - Crohn’s disease
KW - Inflammatory bowel disease
KW - Irritable bowel syndrome
KW - Single-nucleotide polymorphisms
KW - Ulcerative colitis
UR - https://www.scopus.com/pages/publications/85100655222
U2 - 10.1186/s12876-021-01622-x
DO - 10.1186/s12876-021-01622-x
M3 - Article
C2 - 33546600
AN - SCOPUS:85100655222
SN - 1471-230X
VL - 21
JO - BMC Gastroenterology
JF - BMC Gastroenterology
IS - 1
M1 - 53
ER -