TY - JOUR
T1 - Short chain fatty acid rectal irrigation for left-sided ulcerative colitis
T2 - A randomised, placebo controlled trial
AU - Breuer, R. I.
AU - Soergel, K. H.
AU - Lashner, B. A.
AU - Christ, M. L.
AU - Hanauer, S. B.
AU - Vanagunas, A.
AU - Harig, J. M.
AU - Keshavarzian, A.
AU - Robinson, M.
AU - Sellin, J. H.
AU - Weinberg, D.
AU - Vidican, D. E.
AU - Flemal, K. L.
AU - Rademaker, A. W.
PY - 1997
Y1 - 1997
N2 - Background - Short chain fatty acid (SCFA) deficiency is associated with colitis in animals and humans, and the mucosal metabolism of these compounds is decreased in ulcerative colitis. Aims - To assess the efficacy of topical SCFA treatment in ulcerative colitis. Patients and Methods - 103 patients with distal ulcerative colitis were entered into a six week, double-blind, placebo controlled trial of rectal SCFA twice daily; patients who were unchanged on placebo were offered SCFA in an open-label extension trial. Results - Of the 91 patients completing the trial, more patients in the SCFA treated than in the placebo treated group improved (33% v 20%, p = 0.14, NS). Those on SCFA also had larger, but statistically non-significant, reductions in every component of their clinical and histological activity scores. In patients with a relatively short current episode of colitis (<6 months, n = 42), more responded to SCFA than to placebo (48% v 18%, p = 0.03). These patients also had larger, but statistically non-significant, decreases in their clinical activity index (p = 0.08 v placebo). Every patient who improved used at least five of six of the prescribed rectal SCFA irrigations, whereas only 37% who did not improve were as compliant. In the open-label extension trial, 65% improved on SCFA; these patients also had significant reductions (p < 0.02) in their clinical and histological activity scores. Conclusions - Although SCFA enemas were not of therapeutic value in this controlled trial, the results suggest efficacy in subsets of patients with distal ulcerative colitis including those with short active episodes. Prolonged contact with rectal mucosa seems to be necessary for therapeutic benefit.
AB - Background - Short chain fatty acid (SCFA) deficiency is associated with colitis in animals and humans, and the mucosal metabolism of these compounds is decreased in ulcerative colitis. Aims - To assess the efficacy of topical SCFA treatment in ulcerative colitis. Patients and Methods - 103 patients with distal ulcerative colitis were entered into a six week, double-blind, placebo controlled trial of rectal SCFA twice daily; patients who were unchanged on placebo were offered SCFA in an open-label extension trial. Results - Of the 91 patients completing the trial, more patients in the SCFA treated than in the placebo treated group improved (33% v 20%, p = 0.14, NS). Those on SCFA also had larger, but statistically non-significant, reductions in every component of their clinical and histological activity scores. In patients with a relatively short current episode of colitis (<6 months, n = 42), more responded to SCFA than to placebo (48% v 18%, p = 0.03). These patients also had larger, but statistically non-significant, decreases in their clinical activity index (p = 0.08 v placebo). Every patient who improved used at least five of six of the prescribed rectal SCFA irrigations, whereas only 37% who did not improve were as compliant. In the open-label extension trial, 65% improved on SCFA; these patients also had significant reductions (p < 0.02) in their clinical and histological activity scores. Conclusions - Although SCFA enemas were not of therapeutic value in this controlled trial, the results suggest efficacy in subsets of patients with distal ulcerative colitis including those with short active episodes. Prolonged contact with rectal mucosa seems to be necessary for therapeutic benefit.
KW - Distal ulcerative colitis
KW - Short chain fatty acids
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U2 - 10.1136/gut.40.4.485
DO - 10.1136/gut.40.4.485
M3 - Article
C2 - 9176076
AN - SCOPUS:8244260090
SN - 0017-5749
VL - 40
SP - 485
EP - 491
JO - Gut
JF - Gut
IS - 4
ER -