Prognosis of ursodeoxycholic Acid-treated patients with primary biliary cirrhosis. Results of a 10-yr cohort study involving 297 patients
- PMID: 16848809
- DOI: 10.1111/j.1572-0241.2006.00699.x
Prognosis of ursodeoxycholic Acid-treated patients with primary biliary cirrhosis. Results of a 10-yr cohort study involving 297 patients
Abstract
Background and aims: The therapeutic potential of ursodeoxycholic acid (UDCA) treatment in primary biliary cirrhosis (PBC) remains controversial. In addition, relatively few data have been reported on the outcome of patients who have been treated long term. The aim of the present study was to document long-term survival of a prospectively followed large cohort of UDCA treated patients in comparison to that predicted by the Mayo model and of a matched control cohort of the Dutch population.
Methods: Two hundred ninety-seven patients were included and followed during a median period of 68 (range 3-126) months until death or the end of the study.
Results: Survival free of transplantation (1 yr 99.7%, 5 yr 87%, and 10 yr 71%) was significantly better than predicted by the Mayo model (p= 0.01). However, for patients with abnormal serum bilirubin and/or albumin concentrations at entry, observed and predicted survival did not significantly differ. Compared with survival for a standardized cohort of the Dutch population, observed survival for the total group was significantly decreased (p= 0.0003); for noncirrhotic patients and patients with normal entry bilirubin and albumin concentrations survival was comparable. Serum bilirubin and albumin concentrations were the prognostic factors most consistently associated with survival.
Conclusions: A 10-year prognosis for most UDCA-treated patients with PBC, i.e., those with a normal bilirubin and albumin concentration, is comparable to that of a matched general population. Our finding that observed survival was significantly better than predicted by the Mayo model may suggest that this model did not accurately predict prognosis in our cohort. Alternatively, this finding indicates an important therapeutic effect of long-term UDCA treatment in PBC, particularly in patients with noncirrhotic, nonadvanced disease.
Comment in
-
What is the influence of long-term ursodeoxycholic acid therapy in patients with primary biliary cirrhosis?Nat Clin Pract Gastroenterol Hepatol. 2007 Apr;4(4):188-9. doi: 10.1038/ncpgasthep0741. Epub 2007 Feb 6. Nat Clin Pract Gastroenterol Hepatol. 2007. PMID: 17290236 No abstract available.
Similar articles
-
Improved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid.Gastroenterology. 2009 Apr;136(4):1281-7. doi: 10.1053/j.gastro.2009.01.003. Epub 2009 Jan 14. Gastroenterology. 2009. PMID: 19208346
-
Ten-year survival in ursodeoxycholic acid-treated patients with primary biliary cirrhosis. The UDCA-PBC Study Group.Hepatology. 1999 Jun;29(6):1668-71. doi: 10.1002/hep.510290603. Hepatology. 1999. PMID: 10347106 Clinical Trial.
-
Clinical significance of serum bilirubin levels under ursodeoxycholic acid therapy in patients with primary biliary cirrhosis.Hepatology. 1999 Jan;29(1):39-43. doi: 10.1002/hep.510290140. Hepatology. 1999. PMID: 9862847 Clinical Trial.
-
The natural history of PBC: has it changed?Semin Liver Dis. 2005 Aug;25(3):321-6. doi: 10.1055/s-2005-916323. Semin Liver Dis. 2005. PMID: 16143947 Review.
-
Liver transplantation for primary biliary cirrhosis and primary sclerosing cholangitis: does medical treatment alter timing and selection?Liver Transpl Surg. 1998 Sep;4(5 Suppl 1):S9-17. Liver Transpl Surg. 1998. PMID: 9742489 Review.
Cited by
-
Primary biliary cirrhosis.Orphanet J Rare Dis. 2008 Jan 23;3:1. doi: 10.1186/1750-1172-3-1. Orphanet J Rare Dis. 2008. PMID: 18215315 Free PMC article. Review.
-
Prognostic Factors for Transplant-Free Survival and Validation of Prognostic Models in Chinese Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid.Clin Transl Gastroenterol. 2017 Jun 22;8(6):e100. doi: 10.1038/ctg.2017.23. Clin Transl Gastroenterol. 2017. PMID: 28640288 Free PMC article.
-
Underestimated Male Prevalence of Primary Biliary Cholangitis in China: Results of a 16-yr cohort study involving 769 patients.Sci Rep. 2017 Jul 26;7(1):6560. doi: 10.1038/s41598-017-06807-7. Sci Rep. 2017. PMID: 28747696 Free PMC article.
-
The Management of Cholestatic Liver Diseases: Current Therapies and Emerging New Possibilities.J Clin Med. 2021 Apr 18;10(8):1763. doi: 10.3390/jcm10081763. J Clin Med. 2021. PMID: 33919600 Free PMC article. Review.
-
Bile acid therapy for primary biliary cholangitis: Pathogenetic validation.World J Exp Med. 2025 Mar 20;15(1):101771. doi: 10.5493/wjem.v15.i1.101771. eCollection 2025 Mar 20. World J Exp Med. 2025. PMID: 40115760 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical