Living-donor liver transplantation for autoimmune hepatitis and autoimmune hepatitis-primary biliary cirrhosis overlap syndrome

11Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Aim: Recurrent autoimmune hepatitis (AIH) following liver transplantation has been reported in 20-30% of cases, mainly of Western populations. The aim of this study was to review our experience of living-donor liver transplantation (LDLT) in Japanese patients with AIH. Methods: Among 375 adult (age ≥18years) LDLT performed at our center between 1996 and 2010, 16 (4.2%) were for patients with AIH (n=12) or AIH-primary biliary cirrhosis overlap syndrome (n=4). The patient and donor characteristics and post-transplantation course were reviewed. Results: All recipients were female with a median age of 48years (range, 21-58). Low-dose methylprednisolone and calcineurin inhibitors were continued in all patients. Acute cellular rejection occurred in 10 (63%), which was more frequent than in our overall series of 28.5% (107/375 cases). Overall survival rate was 81.2% at 5years. At the end of the follow up (median, 6.0years [range, 0.1-9.6]), 13 patients were alive with normal liver function tests (aspartate transaminase, 18±5IU/mL; alanine transaminase, 16±8IU/mL). None of the survivors exhibited liver function test results suspicious for recurrent AIH, which might indicate liver biopsy. Conclusion: Survival after LDLT for AIH and overlap syndrome was excellent and there was no evidence of clinical recurrence. The recurrence rate of AIH after liver transplantation may differ among countries, and requires further investigation. © 2012 The Japan Society of Hepatology.

Cite

CITATION STYLE

APA

Yamashiki, N., Sugawara, Y., Tamura, S., Kaneko, J., Takazawa, Y., Aoki, T., … Kokudo, N. (2012). Living-donor liver transplantation for autoimmune hepatitis and autoimmune hepatitis-primary biliary cirrhosis overlap syndrome. Hepatology Research, 42(10), 1016–1023. https://doi.org/10.1111/j.1872-034X.2012.01018.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free