High-Dose Ursodeoxycholic Acid Is Associated With the Development of Colorectal Neoplasia in Patients With Ulcerative Colitis and Primary Sclerosing Cholangitis

被引:180
作者
Eaton, John E. [2 ]
Silveira, Marina G. [1 ]
Pardi, Darrell S. [1 ]
Sinakos, Emmanouil [1 ]
Kowdley, Kris V. [3 ]
Luketic, Velimir A. C. [4 ]
Harrison, M. Edwyn [6 ]
McCashland, Timothy [5 ]
Befeler, Alex S. [7 ]
Harnois, Denise [8 ]
Jorgensen, Roberta [1 ]
Petz, Jan [1 ]
Lindor, Keith D. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Internal Med, Rochester, MN 55905 USA
[3] Virginia Mason Med Ctr, Ctr Liver Dis, Seattle, WA 98101 USA
[4] Virginia Commonwealth Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Richmond, VA USA
[5] Univ Nebraska, Dept Internal Med, Lincoln, NE USA
[6] Mayo Clin, Div Gastroenterol & Hepatol, Scottsdale, AZ USA
[7] St Louis Univ, Div Gastroenterol & Hepatol, St Louis, MO 63103 USA
[8] Mayo Clin, Div Gastroenterol & Hepatol, Jacksonville, FL 32224 USA
关键词
COLON-CANCER CELLS; INFLAMMATORY-BOWEL-DISEASE; LOW-GRADE DYSPLASIA; BILE-ACIDS; LITHOCHOLIC ACID; DEOXYCHOLIC-ACID; CARCINOGENESIS; APOPTOSIS; RISK; POLYPECTOMY;
D O I
10.1038/ajg.2011.156
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Some studies have suggested that ursodeoxycholic acid (UDCA) may have a chemopreventive effect on the development of colorectal neoplasia in patients with ulcerative colitis (UC) and primary sclerosing cholangitis (PSC). We examined the effects of high-dose (28-30 mg/kg/day) UDCA on the development of colorectal neoplasia in patients with UC and PSC. METHODS: Patients with UC and PSC enrolled in a prior, multicenter randomized placebo-controlled trial of high-dose UDCA were evaluated for the development of colorectal neoplasia. Patients with UC and PSC who received UDCA were compared with those who received placebo. We reviewed the pathology and colonoscopy reports for the development of low-grade or high-grade dysplasia or colorectal cancer. RESULTS: Fifty-six subjects were followed for a total of 235 patient years. Baseline characteristics (including duration of PSC and UC, medications, patient age, family history of colorectal cancer, and smoking status) were similar for both the groups. Patients who received high-dose UDCA had a significantly higher risk of developing colorectal neoplasia (dysplasia and cancer) during the study compared with those who received placebo (hazard ratio: 4.44, 95% confidence interval: 1.30-20.10, P=0.02). CONCLUSIONS: Long-term use of high-dose UDCA is associated with an increased risk of colorectal neoplasia in patients with UC and PSC.
引用
收藏
页码:1638 / 1645
页数:8
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