Document Type
Article
Publication Date
12-1-2012
Abstract
BACKGROUND: Epigallocatechin-3-gallate (EGCG) has antiangiogenic, antioxidant, and antifibrotic properties that may have therapeutic potential for the treatment of cirrhosis induced by hepatitis C virus (HCV). However, cirrhosis might affect EGCG disposition and augment its reported dose-dependent hepatotoxic potential.
OBJECTIVE: The safety, tolerability, and disposition of a single oral dose of EGCG in cirrhotic patients with HCV were examined in an exploratory fashion.
METHODS: Eleven patients with hepatitis C and detectable viremia were enrolled. Four had Child-Pugh (CP) class A cirrhosis, 4 had Child-Pugh class B cirrhosis, and 3 were noncirrhotic. After a single oral dose of green tea extract 400 mg containing 94% pure EGCG, blood for EGCG levels and safety parameters was ascertained at 2, 4, and 10 hours.
RESULTS: C(max) and AUC to EGCG overlapped among the 3 groups, which suggests that the disposition of EGCG was not significantly altered in these patients with cirrhosis.
CONCLUSIONS: A single 400-mg oral dose of EGCG was safe and well tolerated by all of the patients in the study. These results provide guidance for the continued investigation of the long-term safety and antitumor potential of EGCG in cirrhotic patients with HCV.
Recommended Citation
Halegoua-De Marzio, Dina; Kraft, Walter K.; Daskalakis, Constantine; Ying, Xie; Hawke, Roy L; and Navarro, Victor J., "Limited sampling estimates of epigallocatechin gallate exposures in cirrhotic and noncirrhotic patients with hepatitis C after single oral doses of green tea extract." (2012). Division of Gastroenterology and Hepatology Faculty Papers. Paper 17.
https://jdc.jefferson.edu/gastro_hepfp/17
PubMed ID
23153661
Included in
Biostatistics Commons, Gastroenterology Commons, Hepatology Commons, Pharmacy and Pharmaceutical Sciences Commons
Comments
This article has been peer reviewed. It is the authors' final version prior to publication in Clinical Therapeutics
Volume 34, Issue 12, December 2012, Pages: 2279-2285e1
The published version is available at . DOI: 10.1016/j.clinthera.2012.10.009. Copyright © Elsevier Inc.