scholarly journals Serum Aspartate Aminotransferase Level and Previous Histopathological Findings Enable Reduction of Protocol Liver Biopsies after Liver Transplantation for Hepatitis C

2013 ◽  
Vol 27 (3) ◽  
pp. 131-136 ◽  
Author(s):  
Tomohiro Tanaka ◽  
George Therapondos ◽  
Nazia Selzner ◽  
Eberhard L Renner ◽  
Leslie B Lilly

BACKGROUND: Hepatitis C virus (HCV) infection remains the leading indication for liver transplantation (LT) worldwide. Recurrent hepatitis C following LT is universal, and significant fibrosis (SF, Metavir fibrosis stage ≥2) apparent on protocol biopsy typically prompts antiviral therapy.OBJECTIVE: To determine the optimal timing of protocol liver biopsies in this setting.METHODS: A total of 151 patients who underwent LT related to HCV infection between July 2004 and December 2009 were analyzed retrospectively. Data regarding protocol liver biopsies at six, 12 and 24 months post-LT, conventional laboratory parameters and demographic information were obtained.RESULTS: The 151 patients included in the present study had significantly lower serum aspartate aminotransferase (AST) levels than the four patients who progressed to receive antiviral treatment for SF before six months post-LT (P<0.001). AST level, but not alanine aminotransferase level, histological activity or fibrosis stage at the six-month biopsy was independently associated with the progression to SF at 12 months (P<0.05). However, AST level, histological activity and fibrosis stage at the 12-month biopsy emerged as independent parameters associated with progression to SF at 24 months (P<0.05).CONCLUSION: The protocol liver biopsy at six months could be eliminated, especially in patients who consistently exhibit low AST levels. Histological activity, the presence or absence of fibrosis, and AST values at the 12-month biopsy may lead to the decision to defer the protocol biopsy at 24 months or result in earlier introduction of antiviral therapy.

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Stenard Fabien ◽  
Morales Olivier ◽  
Ghazal Khaldoun ◽  
Viallon Vivian ◽  
Aoudjehane Lynda ◽  
...  

The TRANSPEG study was a prospective study to assess the efficacy of antiviral therapy in patients with a recurrent hepatitis C virus (HCV) after liver transplantation. The influence of regulatory T-cells (Tregs) on the response to antiviral therapy was analyzed. Patients were considered as a function of their sustained virological response (SVR) at 18 months after treatment initiation. A transcriptomic analysis was performed to assess Treg markers (Tr1 and FoxP3+) in serum, PBMC, and liver biopsies. 100 patients had been included in the TRANSPEG study. Data from 27 of these patients were available. The results showed that the expression of CD49b (a predominant marker of Tr1) before the introduction of antiviral therapy was significantly associated with SVR. Responders displayed lower serum levels of CD49b than nonresponders (P<0.02). These findings were confirmed in PBMC and liver biopsies even if in a nonsignificant manner for the limited number of samples. The assessment of CD49b levels is thus predictive of the response to antiviral therapy. This data suggests that CD49b may be a marker of the failure of the immune response and antiviral therapy during HCV recurrence. The assessment of CD49b could help to select patients who require earlier and more intensive antiviral therapy.


2007 ◽  
Vol 132 (5) ◽  
pp. 1746-1756 ◽  
Author(s):  
José A. Carrión ◽  
Miquel Navasa ◽  
Montserrat García–Retortillo ◽  
Juan Carlos García–Pagan ◽  
Gonzalo Crespo ◽  
...  

2018 ◽  
Vol 69 (4) ◽  
pp. 982-984 ◽  
Author(s):  
Kerstin Herzer ◽  
Guido Gerken ◽  
Daniela Kroy ◽  
Frank Tacke ◽  
Julius Plewe ◽  
...  

2005 ◽  
Vol 79 (3) ◽  
pp. 261-268 ◽  
Author(s):  
Christos Triantos ◽  
Dimitrios Samonakis ◽  
Rosa Stigliano ◽  
Ulrich Thalheimer ◽  
David Patch ◽  
...  

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