Objective: The aim of the present study was to investigate whether corticos
teroid therapy alters gastroduodenal mucosal permeability and whether perme
ability alteration is associated with macroscopic mucosal damage. Methods:
Eight patients taking oral corticosteroid therapy (total prednisone-equival
ent dose, 1.5 +/- 0.1 g; duration, similar to 30 days), nine patients with
multiple sclerosis taking high-dose intravenous methyl-prednisolone therapy
(total dose, 11.7 +/- 0.5 g; duration, similar to 9 days), and 20 age- and
gender-matched controls were studied. Gastroduodenal permeability was dete
rmined using sucrose as a site-specific permeability probe. Five-hour urine
was collected after ingesting 100 g of sucrose and its urinary excretion r
ate was measured using high-pressure liquid chromatography, Gastroduodenal
endoscopy was performed before steroid therapy to exclude subjects with evi
dence of macroscopic mucosal lesions. The sucrose test and endoscopy were r
epeated after completion of corticosteroid therapy. Results: The urinary su
crose excretion rates were similar in the control group and in patient grou
ps before corticosteroid therapy, The median excretion rate of sucrose incr
eased four (one to 28)- and eight (two to 35)-fold, respectively, as compar
ed with pretreatment values in patients taking oral steroid and high-dose i
ntravenous methyl-prednisolone therapy (p < 0.01), Considering all patients
together, subjects who received a mean prednisone-equivalent dose of 8.4 /- 1.5 g exhibited mucosal lesions, whereas patients who received 3.3 +/- 1
.8 g did not (p = 0.06). The posttherapy increments in sucrose excretion ra
tes were associated with neither the presence of macroscopic lesions nor wi
th the total steroid dose received. Conclusions: Corticosteroid therapy aug
ments gastroduodenal permeability and high doses are associated,vith macros
copic mucosal lesions. Steroid-induced permeability increase does not appea
r to be associated with the presence of macroscopic mucosal lesions. (C) 19
98 by Am. Coll. of Gastroenterology.