Randomized, placebo-controlled trial of gastric acid-lowering therapy on duodenal polyposis and relative adduct labeling in familial adenomatous polyposis

PURPOSE:Bile has been implicated in the pathogenesis of duodenal polyps in patients with familial adenomatous polyposis. In vitro experiments have shown that familial adenomatous polyposis bile is capable of producing DNA adducts. This effect can be ameliorated by increasing the pH of the incubate....

Full description

Saved in:
Bibliographic Details
Published inDiseases of the colon & rectum Vol. 44; no. 11; pp. 1585 - 1589
Main Authors Wallace, Marina H, Forbes, Alastair, Beveridge, Iain G, Spigelman, Allan D, Hewer, Alan, Venitt, Stan, Phillips, Robin K. S
Format Journal Article Conference Proceeding
LanguageEnglish
Published Secaucus, NJ The ASCRS 01.11.2001
Springer
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:PURPOSE:Bile has been implicated in the pathogenesis of duodenal polyps in patients with familial adenomatous polyposis. In vitro experiments have shown that familial adenomatous polyposis bile is capable of producing DNA adducts. This effect can be ameliorated by increasing the pH of the incubate. The aim of this double-blind randomized placebo-controlled trial was to examine the effect of oral ranitidine on duodenal polyposis in a group of patients with familial adenomatous polyposis. METHODS:Twenty-six patients with familial adenomatous polyposis were randomly assigned to ranitidine 300 mg daily or placebo for six months after baseline endoscopy. Polyp counts were performed and biopsy specimens taken to detect DNA adducts byP-postlabeling. RESULTS:No difference was seen in polyp numbers (P =0.9) or relative adduct labeling (P =0.7) after treatment with ranitidine or placebo. DISCUSSION:Acid suppression therapy does not seem to improve duodenal polyposis despite in vitro findings. On the other hand, ranitidine does not exacerbate actual (or markers of) neoplasia in this highly tumor-prone condition.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
ObjectType-News-3
content type line 23
ISSN:0012-3706
1530-0358
DOI:10.1007/BF02234376