Treatment With Ursodeoxycholic Acid Is Associated With Weight Gain in Patients With Primary Biliary Cirrhosis

Background Ursodeoxycholic acid (UDCA) is the established treatment of primary biliary cirrhosis (PBC) and is a safe and well-tolerated medication. Nevertheless, patients often anecdotally complain of weight gain while on this drug. Goals We compared weight changes in patients treated with UDCA and those on placebo to characterize this potential side effect. Study One-hundred eighty patients with PBC who were enrolled into a randomized, controlled trial received either UDCA (13–15 mg/kg/d) or an identical placebo. Changes from baseline weight were calculated at 12, 24, 36, and 48 months. Other markers of disease activity, including liver biochemistries, serum lipids, histologic stage, and Mayo Risk Score were evaluated in both groups. Results The proportion of patients who gained weight during the first 12 months of therapy was significantly greater in the UDCA than placebo group (67/86 [78%] versus 43/73 [57%] respectively, P = 0.005). Patients in the UDCA group gained an average of 3.6 ± 6.5% kg (2.2 ± 5.1 kg) which was significantly greater than the average of 0.6 ± 6.9% kg (0.6 ± 4.9 kg) gained in the placebo group (P = 0.04). The biggest change in weight occurred in the first 12 months of treatment (P < 0.001); after this, weight was maintained for the 4-year duration of treatment. There was no significant correlation between initial body mass index (BMI) and weight change or changes in disease activity and weight. Conclusion UDCA treatment in patients with PBC is associated with a significant weight gain that occurs in the first 12 months of treatment, persists for the duration of treatment, and occurs independent of baseline BMI. Discussions with PBC patients beginning UDCA treatment should include the beneficial effects this medication has on disease outcome, but should also mention weight gain as a possible side effect.

[1]  K. Lindor,et al.  Relationship of serum cytokines and severity of liver damage in patients with nonalcoholic steatohepatitis , 2001 .

[2]  P. Angulo,et al.  Insulin resistance and mitochondrial abnormalities in NASH: a cool look into a burning issue. , 2001, Gastroenterology.

[3]  H. Tilg,et al.  Cytokines in alcoholic and nonalcoholic steatohepatitis. , 2000, The New England journal of medicine.

[4]  M. Davis,et al.  Cachexia and anorexia: cancer's covert killer , 2000, Supportive Care in Cancer.

[5]  G. Gores,et al.  Mechanisms of cell injury and death in cholestasis and hepatoprotection by ursodeoxycholic acid , 2000 .

[6]  T. Therneau,et al.  Comparison of three doses of ursodeoxycholic acid in the treatment of primary biliary cirrhosis: a randomized trial. , 1999, Journal of hepatology.

[7]  T. Therneau,et al.  Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acid. , 1999, Liver.

[8]  T. Therneau,et al.  Long-term ursodeoxycholic acid delays histological progression in primary biliary cirrhosis. , 1999, Hepatology.

[9]  C. Defilippi,et al.  Small bowel motility in primary biliary cirrhosis , 1998, American Journal of Gastroenterology.

[10]  J. DiBaise,et al.  Steatorrhea and weight loss in a 72-year-old man , 1998 .

[11]  E. Dickson,et al.  Autoimmune conditions associated with primary biliary cirrhosis: response to ursodeoxycholic acid therapy , 1998, American Journal of Gastroenterology.

[12]  F. López‐Soriano,et al.  Journey from cachexia to obesity by TNF , 1997, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[13]  E. Dickson,et al.  Ursodeoxycholic acid in the treatment of primary biliary cirrhosis. , 1994, Gastroenterology.

[14]  M. Kaplan,et al.  Abdominal pain after taking ursodiol. , 1993, The New England journal of medicine.

[15]  R. Workman,et al.  Primary biliary cirrhosis and adult celiac disease. , 1992, The Western journal of medicine.

[16]  W. Behr,et al.  Adult celiac disease and primary biliary cirrhosis. , 1986, The American journal of gastroenterology.

[17]  P. Amoroso,et al.  Delta infection in the Naples area. Epidemiologic and clinical significance. , 1986, Journal of hepatology.

[18]  E. Dickson,et al.  Pathogenesis of steatorrhea in primary biliary cirrhosis , 1985, Hepatology.

[19]  J. Boyer,et al.  The prognostic importance of clinical and histologic features in asymptomatic and symptomatic primary biliary cirrhosis. , 1983, The New England journal of medicine.

[20]  G. Beckett,et al.  Weight loss in primary biliary cirrhosis. , 1980, Gut.

[21]  D. Owen,et al.  An association between primary biliary cirrhosis and jejunal villous atrophy resembling celiac disease , 1979, Digestive diseases and sciences.

[22]  A. Ferguson,et al.  PRIMARY BILIARY CIRRHOSIS AND CŒLIAC DISEASE An Association? , 1978, The Lancet.

[23]  S. Sherlock,et al.  The presentation and diagnosis of 100 patients with primary biliary cirrhosis. , 1973, The New England journal of medicine.