Entecavir; 3. Quasispecies; 4. Evolution; Presenting Author: HE BING Additional Authors: YANG SHI-MING Corresponding Author: YANG SHI-MING Affiliations: Department of Gastroenterology, XinQiao Hospital Objective: Severe

viral hepatitis B is a disease associated with significant morbidity and mortality. Clinical controlled trials show that the efficacy of treatment of severe viral hepatitis B with glucocorticoids remains debatable. Therefore, we carried out this meta-analysis to evaluate the safety, efficacy, and side effects of glucocorticoid therapy for severe viral hepatitis B. Methods: We searched PubMed, Medline, Embase, Cochrane Library, and Google Scholar for randomized-controlled trials published before April 2012 in which glucocorticoid therapy was compared with routine treatment for severe viral hepatitis Midostaurin B. The primary outcome was the survival rate of the two groups. Results: We selected eight controlled clinical trials, which included 597 patients. We recorded a benefit of glucocorticoid treatment on the survival rate of patients with severe viral hepatitis B (597 patients) [risk ratio (RR) = 1.188, 95% confidence

interval (CI) 1.030–1.369, P = 0.018]. The benefit was most noticeable in patients at the stage of preliver failure (409 patients) (RR = 1.275, 95%CI 1.077–1.510, Tamoxifen P = 0.005), whereas there was no efficacy for patients with liver failure (188 patients) (RR = 1.008, 95%CI 0.774–1.312, P = 0.955). Glucocorticoid treatment was not associated with the development of secondary

infection and bleeding. Conclusion: Treatment with glucocorticoids can significantly increase the survival rate of patients with severe hepatitis B. The benefit was most noticeable in patients at the stage of preliver failure. However, the incidence of secondary infection and bleeding did not change significantly. This finding suggests that prompt and timely glucocorticoid treatment is crucial. Oxymatrine Key Word(s): 1. Glucocorticoids; 2. HBV; 3. hepatitis; 4. survival rate; Presenting Author: NONG-RONGNONG WANG Additional Authors: HUAN DENG Corresponding Author: HUAN DENG Affiliations: The Fourth Affiliated Hospital of Nanchang University Objective: The origin and heterogeneity of hepatic progenitor cells (HPCs) remain unclear. This study was to determine whether HPCs derive from cholangiocytes and/or hepatocytes via epithelial-mesenchymal transition (EMT) in hepatitis B virus (HBV)-related liver diseases. Methods: Surgical liver specimens from 75 cases of HBV-related diseases were subjected to electron microscopic (EM) examination. Immunohistochemical (IHC) investigations with double labeling were performed in 60 cases to detect the existence of HPCs (NCAM), epithelial cells (CK7 and E-cadherin), epithelial-mesenchymal transition (TGF-β, S100A4, MMP-2 and vimentin), myofibroblasts (αSMA), and T-cells (CD3). As control, 5 and 10 cases of normal liver from the patients with spleen-trauma operation were EM and IHC studied respectively.