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dc.contributor.authorEl-Salhy, Magdyen_US
dc.contributor.authorGilja, Odd Helgeen_US
dc.contributor.authorGundersen, Doris Ireneen_US
dc.contributor.authorHatlebakk, Jan Gen_US
dc.contributor.authorHausken, Trygveen_US
dc.date.accessioned2015-09-23T07:20:59Z
dc.date.available2015-09-23T07:20:59Z
dc.date.issued2014-03-07
dc.identifier.issn1007-9327
dc.identifier.urihttps://hdl.handle.net/1956/10505
dc.description.abstractAIM: To study the ileal endocrine cell types in irritable bowel syndrome (IBS) patients. METHODS: Ninety-eight patients with IBS (77 females and 21 males; mean age 35 years, range 18-66 years) were included, of which 35 patients had diarrhea (IBS-D), 31 patients had a mixture of both diarrhea and constipation (IBS-M), and 32 patients had constipation (IBS-C) as the predominant symptoms. The controls were 38 subjects (26 females and 12 males; mean age 40 years, range 18-65 years) who had submitted to colonoscopy for the following reasons: gastrointestinal bleeding, where the source of bleeding was identified as hemorrhoids (n = 24) or angiodysplasia (n = 3), and health worries resulting from a relative being diagnosed with colon carcinoma (n = 11). The patients were asked to complete the: Birmingham IBS symptom questionnaire. Ileal biopsy specimens from all subjects were immunostained using the avidin-biotin-complex method for serotonin, peptide YY (PYY), pancreatic polypeptide (PP), enteroglucagon, and somatostatin cells. The cell densities were quantified by computerized image analysis, using Olympus cellSens imaging software. RESULTS: The gender and age distributions did not differ significantly between the patients and the controls (P = 0.27 and P = 0.18, respectively). The total score of Birmingham IBS symptom questionnaire was 21 ± 0.8, and the three underlying dimensions: pain, diarrhea, and constipation were 7.2 ± 0.4, 6.6 ± 0.4, and 7.2 ± 0.4, respectively. The density of serotonin cells in the ileum was 40.6 ± 3.6 cells/mm2 in the controls, and 11.5 ± 1.2, 10.7 ± 5.6, 10.0 ± 1.9, and 13.9 ± 1.4 cells/mm2 in the all IBS patients (IBS-total), IBS-D, IBS-M, and IBS-C patients, respectively. The density in the controls differed significantly from those in the IBS-total, IBS-D, IBS-M, and IBS-C groups (P < 0.0001, P = 0.0001, P = 0.0001, and P < 0.0001, respectively). There was a significant inverse correlation between the serotonin cell density and the pain dimension of Birmingham IBS symptom questionnaire (r = -0.6, P = 0.0002). The density of PYY cells was 26.7 ± 1.6 cells/mm2 in the controls, and 33.1 ± 1.4, 27.5 ± 1.4, 34.1 ± 2.5, and 41.7 ± 3.1 cells/mm2 in the IBS-total, IBS-D, IBS-M, and IBS-C patients, respectively. This density differed significantly between patients with IBS-total and IBS-C and the controls (P = 0.03 and < 0.0001, respectively), but not between controls and, IBS-D, and IBS-M patients (P = 0.8, and P = 0.1, respectively). The density of PYY cells correlated significantly with the degree of constipation as recorded by the Birmingham IBS symptom questionnaire (r = 0.6, P = 0.0002). There were few PP-, enteroglucagon-, and somatostatin-immunoreactive cells in the biopsy material examined, which made it impossible to reliably quantify these cells. CONCLUSION: The decrease of ileal serotonin cells is associated with the visceral hypersensitivity seen in all IBS subtypes. The increased density of PYY cells in IBS-C might contribute to the constipation experienced by these patients.en_US
dc.language.isoengeng
dc.publisherBaishideng Publishing Groupeng
dc.rightsAttribution CC BY-NCeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/eng
dc.subjectComputer image analysiseng
dc.subjectIrritable bowel syndromeeng
dc.subjectIleumeng
dc.subjectPeptide YYeng
dc.subjectSerotonineng
dc.titleEndocrine cells in the ileum of patients with irritable bowel syndromeen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2015-07-28T08:25:03Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2014 Baishideng Publishing Group
dc.identifier.doihttps://doi.org/10.3748/wjg.v20.i9.2383
dc.identifier.cristin1118933
dc.source.journalWorld Journal of Gastroenterology
dc.source.4020
dc.source.149
dc.source.pagenumber2383-2391
dc.subject.nsiVDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Gasteroenterologi: 773
dc.subject.nsiVDP::Midical sciences: 700::Clinical medical sciences: 750::Gastroenterology: 773


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