As. Taha et al., DOES CHOLESTYRAMINE REDUCE THE EFFICACY OF URSODEOXYCHOLIC ACID IN PRIMARY BILIARY-CIRRHOSIS, European journal of gastroenterology & hepatology, 6(6), 1994, pp. 535-538
Ursodeoxycholic acid (UDCA) has been accepted for its efficacy in the
treatment of primary biliary cirrhosis. It is not clear whether such b
enefit is compromised in patients who use cholestyramine for pruritus.
Aims and methods: To study serum bile acid levels, liver function tes
ts, and the degree of pruritus in eight patients with primary biliary
cirrhosis with histological stages 1-111. The study was divided into f
our consecutive phases each lasting 2 weeks: (1) cholestyramine alone;
(2) wash-out period; (3) UDCA alone, and (4) both agents taken 5 h ap
art. Results: UDCA with or without cholestyramine significantly reduce
d alkaline phosphatase and gamma-glutamyl transpeptidase activities. T
he median visual analogue score of pruritus rose from 1 6 mm at the en
d of cholestyramine alone to 31 mm in the wash-out period, 25 mm on UD
CA alone, and 24 mm on combined treatment. The median serum level of g
lycoursodeoxycholic acid was 22 mumol/l during UDCA therapy compared w
ith 6 mumol/l during cholestyramine therapy (P = 0.02), 7 mumol/l duri
ng the washout phase (P = 0.02), and 19 mumol/l during combined treatm
ent (P = 0.04). The increase in the levels and proportions of UDCA con
jugates was accompanied by a relative fall in the proportions of the p
rimary bile acids when UDCA was taken with or without cholestyramine.
Conclusion: The beneficial activities of UDCA (improving liver functio
n tests, reducing pruritus, and increasing UDCA conjugates) could stil
l be preserved in primary biliary cirrhosis patients who use cholestyr
amine, at least in the short-term when the two agents are taken at lea
st 5 h apart.