Back to Search Start Over

Randomized, double-blind, placebo-controlled trial of prednisolone in post-infectious irritable bowel syndrome.

Authors :
Dunlop, S. P.
Jenkins, D.
Neal, K. R.
Naesdal, J.
Borgaonker, M.
Collins, S. M.
Spiller, R. C.
Source :
Alimentary Pharmacology & Therapeutics. Jul2003, Vol. 18 Issue 1, p77-84. 8p. 3 Charts.
Publication Year :
2003

Abstract

Summary Background : Post-infectious irritable bowel syndrome is associated with increased serotonin-containing enterochromaffin cells and lymphocytes in rectal biopsies. Animal studies have suggested that steroids reduce the lymphocyte response and suppress some of the post-infectious changes in neuromuscular function. Aim : To evaluate whether steroids reduce the number of enterochromaffin cells and improve the symptoms of post-infectious irritable bowel syndrome. Methods : Twenty-nine patients with post-infectious irritable bowel syndrome underwent a randomized, double-blind, placebo-controlled trial of 3 weeks of oral prednisolone, 30 mg/day. Mucosal enterochromaffin cells, T lymphocytes and mast cells were assessed in rectal biopsies before and after treatment, and bowel symptoms were recorded in a daily diary. Results: Initial enterochromaffin cell counts were increased and correlated with initial lamina propria T-lymphocyte counts (r = 0.460, P = 0.014). Enterochromaffin cell counts did not change significantly after either prednisolone (- 0.8% ± 9.2%) or placebo (7.9% ± 7.9%) (P = 0.5). Although lamina propria T-lymphocyte counts decreased significantly after prednisolone (22.0% ± 5.6%, P = 0.003), but not after placebo (11.5% ± 8.6%, P = 0.1), this was not associated with any significant treatment-related improvement in abdominal pain, diarrhoea, frequency or urgency. Conclusions : Prednisolone does not appear to reduce the number of enterochromaffin cells or cause an improvement in symptoms in post-infectious irritable bowel syndrome. Other approaches to this persistent condition are indicated. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02692813
Volume :
18
Issue :
1
Database :
Academic Search Index
Journal :
Alimentary Pharmacology & Therapeutics
Publication Type :
Academic Journal
Accession number :
10193612
Full Text :
https://doi.org/10.1046/j.1365-2036.2003.01640.x