Ursodeoxycholic acid for primary sclerosing cholangitis

J Hepatol. 1990 Jul;11(1):120-3. doi: 10.1016/0168-8278(90)90281-u.

Abstract

The effects of ursodeoxycholic acid (UDCA, 750-1250 mg/day) were evaluated prospectively in 15 patients with primary sclerosing cholangitis (PSC). Five patients had associated inflammatory bowel disease. After 6 months of treatment, the proportion of patients suffering from fatigue or pruritus decreased from 60% to 20% and from 33% to 20%, respectively. No exacerbation of associated disorders was observed. Serum alkaline phosphatase levels (normal less than 100 IU/l) decreased from 401 +/- 53 to 222 +/- 42 (mean +/- S.E.; p less than 0.001), those of gamma-glutamyl transpeptidase, (normal less than 40 IU/l) from 520 +/- 89 to 185 +/- 32 (p less than 0.001) and those of alanine aminotransferases, (normal less than 30 IU/l) from 79 +/- 12 to 42 +/- 6 (p less than 0.02). In three patients, the discontinuation of UDCA was associated with an aggravation of the liver test results. In conclusion, this study shows that 6 months of treatment with UDCA leads to clinical and biochemical improvements in patients with PSC. These results suggest that UDCA could be an effective treatment for PSC, and may justify a controlled therapeutic trial.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alkaline Phosphatase / blood
  • Cholangitis, Sclerosing / blood
  • Cholangitis, Sclerosing / drug therapy*
  • Cholangitis, Sclerosing / pathology
  • Deoxycholic Acid / analogs & derivatives*
  • Female
  • Humans
  • Liver / drug effects
  • Liver / enzymology
  • Liver / pathology
  • Male
  • Middle Aged
  • Time Factors
  • Transaminases / blood
  • Ursodeoxycholic Acid / adverse effects
  • Ursodeoxycholic Acid / therapeutic use*
  • gamma-Glutamyltransferase / blood

Substances

  • Deoxycholic Acid
  • Ursodeoxycholic Acid
  • gamma-Glutamyltransferase
  • Transaminases
  • Alkaline Phosphatase