Cited by 77Liver Diseases and ImmunityPediatric Hepatobiliary Diseases and TreatmentsDrug Transport and Resistance Mechanisms

Characterisation of patients with a complete biochemical response to ursodeoxycholic acid.

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Jorgensen, R A, Dickson, E R, Hofmann, A F, Rossi, S S, Lindor, K D·1995·Gut

Abstract

Ursodeoxycholic acid (UDCA) leads to biochemical and clinical improvement in many patients with primary biliary cirrhosis (PBC); although, the response is variable. This study compared UDCA treated patients with complete normalisation of biochemical functions to those without such improvement. Of the 65 patients receiving UDCA, 12 (19%) showed normalisation of liver biochemical functions at two years. The remaining 53 patients showed a less complete response. Mean (SD) alkaline phosphatase and total serum bilirubin values were significantly lower at entry in the patients whose liver biochemistry tests normalised (912 (732) U/l v 1417 (1021) U/l, p = 0.003, and 0.7 (12.1 (5.2) mumol/l v 38.9 (48.5) mumol/l, p = 0.0002, respectively), and percentage of UDCA in biliary bile acid was higher (56.3 (9.5)% v 38.3 (21.1)%, p = 0.03). Patients with biochemically and histologically less severe disease, and greater enrichment of biliary bile with UDCA, are more likely to respond favourably to the drug. The main objective of continued study will be to find out if normal liver biochemical functions can retard disease progression. The association of greater UDCA enrichment with complete biochemical responses suggests that higher doses of UDCA should be evaluated.

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  • About 20% of PBC patients will have normalization of liver biochemistries after 2 years.

    “About 20% of patients will have normalization of liver biochemistries after 2 years. (148)”

    From Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases (2019) · cites this paper as [148]

    The Results report that 12 of 65 patients with PBC receiving ursodeoxycholic acid (19%) had normalized liver biochemical values after two years. This supports the approximate percentage and timing, but the claim omits the treatment condition and reads as applying to PBC patients generally. (LLM, conf=0.88)

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Cites

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Research works printed but not linked: 22

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Authors
Jorgensen, R. A., Dickson, E. R., Hofmann, A. F., Rossi, S. S., & Lindor, K. D.
Affiliations
Mayo Clinic (US)
Venue
Gut
Publisher
BMJ
Published
1995-06
Volume
36
Issue
6
Pages
935-938
ISSN
  • 0017-5749 (ISSN-L)
  • 1468-3288
OpenAlex
W2113962724
Cited by
77
References
1
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 3 · 2013: 2 · 2012: 3
FWCI
4.27
Type
journal article
Language
en
Open access
Locations
  • Gut (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
  • Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
Keywords
ursodeoxycholic acid, primary biliary cirrhosis, biochemical response, treatment response prediction, alkaline phosphatase, serum bilirubin, biliary bile acids, disease severity, disease progression
MeSH terms
Adult, Aged, Alkaline Phosphatase, Bile, Bilirubin, Double-Blind Method, Female, Follow-Up Studies, Humans, Immunoglobulin M, Liver, Liver Cirrhosis, Biliary, Male, Middle Aged, Ursodeoxycholic Acid, Treatment Outcome

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