Ursodiol use is associated with lower prevalence of colonic neoplasia in patients with ulcerative colitis and primary sclerosing cholangitis

Citation
By. Tung et al., Ursodiol use is associated with lower prevalence of colonic neoplasia in patients with ulcerative colitis and primary sclerosing cholangitis, ANN INT MED, 134(2), 2001, pp. 89-95
Citations number
44
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
ANNALS OF INTERNAL MEDICINE
ISSN journal
00034819 → ACNP
Volume
134
Issue
2
Year of publication
2001
Pages
89 - 95
Database
ISI
SICI code
0003-4819(20010116)134:2<89:UUIAWL>2.0.ZU;2-6
Abstract
Background: Patients with ulcerative colitis and primary sclerosing cholang itis are at high risk for colonic dysplasia and cancer. This risk approache s 50% after 25 years of colitis. Ursodiol has been shown to protect against development of colorectal neoplasia in animal models. Objective: To assess the relationship between ursodiol use and colonic dysp lasia, the precursor to colon cancer, in patients with ulcerative colitis a nd primary sclerosing cholangitis. Design: Cross-sectional study. Setting: University medical center. Patients: 59 patients with ulcerative colitis and primary sclerosing cholan gitis who were undergoing colonoscopic surveillance for colonic dysplasia. Measurements: Use of ursodiol was assessed in all patients. The presence or absence of colonic dysplasia was evaluated by colonoscopic surveillance. O ther variables assessed were age at onset and duration of ulcerative coliti s; duration of primary sclerosing cholangitis; Child-Pugh classification; a nd use of sulfasalazine, other 5-aminosalicylic acid preparations, predniso ne, cyclosporine, azathioprine, and methotrexate. Results: Ursodiol use was strongly associated with decreased prevalence of colonic dysplasia (odds ratio, 0.18 [95% CI, 0.05 to 0.61]; P = 0.005). The association between dysplasia and ursodiol use remained after adjustment f or sex, age at onset of colitis, duration of colitis, duration of sclerosin g cholangitis, severity of liver disease, and sulfasalazine use (adjusted o dds ratio, 0.14 [Cl, 0.03 to 0.64]; P = 0.01). Younger age at onset of coli tis was associated with an increased risk for dysplasia. Conclusions: Ursodiol use appears to be associated with a lower frequency o f colonic dysplasia in patients with ulcerative colitis and primary scleros ing cholangitis. A randomized trial investigating the chemoprotective effec t of ursodiol in patients with ulcerative colitis may be warranted.