Glucocorticoids are the mainstay of the medical management of inflamma
tory bower disease (IBD) (Crohn's disease and ulcerative colitis). The
pronounced immunosuppressive capacity of these drugs is closely relat
ed to downregulation of gene expression of proinflammatory and immunor
egulatory cytokines which are produced in increased amounts in active
IBD. The well-known side effects of glucocorticoid treatment have prom
pted the development of a new class of glucocorticoids with high topic
al selectivity for bowel mucosa partly due to high first-pass hepatic
metabolism. Budesonide is the only new steroid which has been extensiv
ely developed for the treatment of inflammatory bower disease. Budeson
ide enemas are as effective as conventional glucocorticoids in the tre
atment of patients with distal ulcerative colitis, but with less adren
al gland suppression. Budesonide controlled ileal release (CIR) capsul
es, which deliver the active drug at the ileocecal region, are superio
r to placebo and only slightly less effective than oral prednisolone i
n the treatment of active Crohn's, but have less glucocorticoid-associ
ated side effects. A similar sustained release formulation for oral tr
eatment of extensive ulcerative colitis is in the development phase. T
hese formulations of budesonide with topical selectivity for inflamed
disease sites seem to represent a real step forward in the management
of selected subgroups of patients with inflammatory bowel disease.