Does antimitochondrial antibody status affect response to treatment in patients with primary biliary cirrhosis? Outcomes of ursodeoxycholic acid therapy and liver transplantation

91Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

Abstract

Approximately 5% to 10% of patients with features otherwise consistent with primary biliary cirrhosis (PBC) lack antimitochondrial antibodies (AMA). Most of these patients have other autoantibodies, a syndrome recently named 'autoimmune cholangitis.' We report our experience in patients with AMA- negative PBC treated with ursodeoxycholic acid (UDCA) and/or liver transplantation (OLT). The study of response to UDCA was performed as follows. While recruiting patients for a previously reported multicenter trial, we identified 8 patients with AMA-negative PBC. The patients were given UDCA and followed up at regular intervals. The characteristics of AMA- negative patients at presentation were similar to those of AMA-positive patients with PBC. The clinical outcomes and sequential liver biochemistries of UDCA treatment were also comparable with those of AMA-positive patients. The study of outcome of OLT was performed as follows. We identified OLT recipients at the Mayo Clinic who had clinical, radiological, and histological features compatible with PBC. Their pretransplant AMA status was determined, and each AMA-negative patient was paired with 2 AMA-positive patients. Of 85 OLT recipients with a diagnosis of PBC, 6 (7.1%) were AMA negative, including 1 who had undergone UDCA therapy. After a median of 36 months of follow-up, graft and patient survival rates and subsequent histological changes (disease recurrence and steroid-resistant or late rejections) were comparable in AMA-negative and -positive PBC patients. In summary, in our experience of 13 AMA-negative PBC patients (including 9 who met the criteria for a diagnosis of autoimmune cholangitis), treatment with UDCA or OLT resulted in similar outcomes to those found in AMA-positive patients. We conclude that AMA status does not affect the response in PBC patients to treatment with UDCA or OLT.

References Powered by Scopus

Ursodiol for the long-term treatment of primary biliary cirrhosis

483Citations
N/AReaders
Get full text

Ursodeoxycholic acid in the treatment of primary biliary cirrhosis

452Citations
N/AReaders
Get full text

Primary Biliary Cirrhosis

324Citations
N/AReaders
Get full text

Cited by Powered by Scopus

International Autoimmune Hepatitis Group Report: Review of criteria for diagnosis of autoimmune hepatitis

2719Citations
N/AReaders
Get full text

Overlap syndromes: The International Autoimmune Hepatitis Group (IAIHG) position statement on a controversial issue

455Citations
N/AReaders
Get full text

Epidemiology and natural history of primary biliary cirrhosis in a U.S. community

324Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Kim, W. R., Poterucha, J. J., Jorgensen, R. A., Batts, K. P., Homburger, H. A., Dickson, E. R., … Lindor, K. D. (1997). Does antimitochondrial antibody status affect response to treatment in patients with primary biliary cirrhosis? Outcomes of ursodeoxycholic acid therapy and liver transplantation. Hepatology, 26(1), 22–26. https://doi.org/10.1002/hep.510260103

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 6

86%

Researcher 1

14%

Readers' Discipline

Tooltip

Medicine and Dentistry 9

90%

Social Sciences 1

10%

Save time finding and organizing research with Mendeley

Sign up for free