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1112A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

1850<br />

Prevalence of hepatitis B core antibody (anti-HBc) and<br />

association with hepatocellular carcinoma (HCC) in<br />

patients with chronic hepatitis C virus (HCV) infection in<br />

the United States (US) and China<br />

Ming Yang 1 , Elizabeth Wu 2 , Sherry Fu 2 , Huiying Rao 1 , Bo Feng 1 ,<br />

Andy Lin 3 , Ran Fei 1 , Neehar D. Parikh 2 , Robert J. Fontana 2 , Anna<br />

S. Lok 2 , Lai Wei 1 ; 1 Peking University People’s Hospital, Peking<br />

University Hepatology Institute, Peking University Health Science<br />

Center, Beijing, China; 2 Division of Gastroenterology, University<br />

of Michigan Health System, Ann Arbor, MI; 3 The Molecular and<br />

Behavioral Neuroscience Institute, University of Michigan, Ann<br />

Arbor, MI<br />

Background: Evidence of previous hepatitis B virus (HBV) infection<br />

[i.e. detectable anti-HBc with undetectable hepatitis B<br />

surface antigen (HBsAg)] has been associated with increased<br />

risk of HCC in patients with chronic HCV infection in many<br />

Asian <strong>studies</strong> but this was not confirmed in some <strong>studies</strong> in the<br />

US. Aims: To compare the prevalence of anti-HBc between US<br />

and Chinese patients with chronic HCV and identify clinical<br />

correlates of anti-HBc positivity. Methods: Prospective study<br />

of 2 cohorts of chronic HCV patients at University of Michigan<br />

in Ann Arbor, US and Peking University People’s Hospital<br />

in urban Beijing and Gu’an and Kuancheng Clinics in rural<br />

Hebei, China. Results: A total of 1,833 patients were analyzed<br />

(963 US; 870 Chinese). 32.3% of US and 46.6% of<br />

Chinese HCV patients were anti-HBc+ and HBsAg- (p0.001).<br />

The prevalence of anti-HBc among patients with chronic hepatitis,<br />

cirrhosis, and HCC was 30.5%, 32.3% and 38.5% in<br />

the US (p=0.250) and 44.5%, 53.8% and 66.7% in China<br />

(p=0.020), respectively. Anti-HBc+ patients were older, had<br />

longer estimated duration of infection and were more likely to<br />

have a history of alcohol and tobacco use in both cohorts. US<br />

anti-HBc+ patients were more likely to be men and to report<br />

a history of injection drug use as the source of infection. In<br />

contrast, Chinese anti-HBc+ patients were more likely to report<br />

medical procedures as the source of infection. Multivariate<br />

analysis showed that there was no association between anti-<br />

HBc positivity and HCC in the US and Chinese cohorts and the<br />

combined cohort. Conclusions: Evidence of previous HBV infection<br />

among patients with chronic HCV is lower in the US cohort<br />

compared to the Chinese cohort. Although the prevalence of<br />

anti-HBc paralleled the severity of HCV-related liver disease,<br />

anti-HBc positivity was not an independent factor associated<br />

with risk of HCC in patients with chronic HCV in both US and<br />

Chinese cohorts.<br />

Characteristics of Patients with and without anti-HBc in the US<br />

and China<br />

Anna S. Lok - Advisory Committees or Review Panels: Gilead, MYR, Tekmira;<br />

Consulting: GSK, Merck; Grant/Research Support: AbbVie, BMS, Gilead, Idenix<br />

Lai Wei - Advisory Committees or Review Panels: Gilead, AbbVie; Grant/<br />

Research Support: BMS<br />

The following authors have nothing to disclose: Ming Yang, Elizabeth Wu, Sherry<br />

Fu, Huiying Rao, Bo Feng, Andy Lin, Ran Fei, Neehar D. Parikh<br />

1851<br />

Wisteria floribunda agglutinin-positive Mac-2-binding<br />

protein predicts hepatocellular carcinoma development<br />

in chronic hepatitis C patients who achieved sustained<br />

virological response to interferon-based anti-viral therapy<br />

Shunsuke Sato, Hironori Tsuzura, Takuya Genda, Akihito Nagahara;<br />

Gastroenterology and Hepatology, Juntendo University Shizuoka<br />

Hospital, Izunokuni, Japan<br />

Objective: The achievement of a sustained virological response<br />

(SVR) after anti-viral therapy reduces the incidence of hepatocellular<br />

carcinoma (HCC) development in patients with chronic<br />

hepatitis C. In advances of direct acting antivirals against hepatitis<br />

C virus, it is expected to drastically increase the patients<br />

with achievement of SVR. However, HCC development in<br />

patients who achieved SVR is not rarely observed. Liver fibrosis<br />

is known as a predictor of HCC development in patients with<br />

achievement of SVR. Although several noninvasive methods<br />

evaluating liver fibrosis has been reported, wisteria floribunda<br />

agglutinin (WFA)-positive Mac-2-binding protein (WFA + -M2BP)<br />

is recently developed as a noninvasive glycobiomarker of liver<br />

fibrosis. The aim of this study is to evaluate WFA + -M2BP as<br />

a predictive marker of HCC development in chronic hepatitis<br />

C patients with achievement of SVR. Methods: A total 280<br />

patients who achieved SVR by interferon-based anti-viral therapy<br />

and underwent measurement of serum WFA + -M2BP level<br />

were enrolled. We compared its usefulness as a predictive<br />

marker of HCC development to other risk factors including age,<br />

gender, body mass index, fibrosis stage, aspartate aminotransferase,<br />

alanine aminotransferase, gamma-glutamyl transpeptidase,<br />

and alpha-fetoprotein (AFP) by using multivariate Cox<br />

proportional hazard analysis. Cumulative incidences of HCC<br />

development were evaluated using Kaplan-Meier plot analysis<br />

and the log-rank test. Results: Serum WFA + -M2BP level was significantly<br />

correlated with liver fibrosis stage (p=0.001). During<br />

the median follow-up time of 4.0 years, 9 of the 280 patients<br />

developed HCC. Multivariate cox proportional hazard analysis<br />

revealed that WFA + -M2BP level was an independent risk factor<br />

of HCC development (hazard ratio (HR): 1.167, 95% confidence<br />

interval (CI): 1.015-1.342, p=0.030) as well as platelet<br />

counts (HR: 0.682, 95%CI: 0.538-0.864, p

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