URSODEOXYCHOLIC ACID FOR PRIMARY SCLEROSING CHOLANGITIS

被引:159
作者
CHAZOUILLERES, O
POUPON, R
CAPRON, JP
METMAN, EH
DHUMEAUX, D
AMOURETTI, M
COUZIGOU, P
LABAYLE, D
TRINCHET, JC
机构
[1] HOP ST ANTOINE,UNITE HEPATOGASTROENTEROL,184 RUE FAUBOURG ST ANTOINE,F-75571 PARIS 12,FRANCE
[2] HOP NORD AMIENS,AMIENS,FRANCE
[3] HOP HENRI MONDOR,F-94010 CRETEIL,FRANCE
[4] HOP TROUSSEAU,TOURS,FRANCE
[5] HOP XAVIER ARNOZAN,PESSAC,FRANCE
[6] HOP LOUISE MICHEL,EVRY,FRANCE
[7] HOP JEAN VERDIER,F-93140 BONDY,FRANCE
关键词
D O I
10.1016/0168-8278(90)90281-U
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 < 100 IU/l) decreased from 401 ± 53 to 222 ± 42 (mean ± S.E.; p < 0.001), those of γ-glutamyl transpeptidase, (normal < 40 IU/l) from 520 ± 89 to 185 ± 32 (p < 0.001) and those of alanine aminotransferases, (normal < 30 IU/l) from 79 ± 12 to 42 ± 6 (p < 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. © 1990.
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页码:120 / 123
页数:4
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