Risk stratification of HBV infection in Asia-Pacific region

Hepatitis B virus (HBV) infection is the major etiology of chronic liver disease worldwide and thus a global health problem, especially in Asia-Pacific region. The long-term outcomes of Asian HBV carriers vary widely; however, a significant proportion of them will finally develop end-stage liver dis...

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Main Author: Jia-Horng Kao
Format: Article
Language:English
Published: Korean Association for the Study of the Liver 2014-09-01
Series:Clinical and Molecular Hepatology
Subjects:
Online Access:http://e-cmh.org/upload/pdf/cmh-20-223.pdf
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author Jia-Horng Kao
author_facet Jia-Horng Kao
author_sort Jia-Horng Kao
collection DOAJ
description Hepatitis B virus (HBV) infection is the major etiology of chronic liver disease worldwide and thus a global health problem, especially in Asia-Pacific region. The long-term outcomes of Asian HBV carriers vary widely; however, a significant proportion of them will finally develop end-stage liver disease. Over the past decade, several host and HBV factors predictive of clinical outcomes in Asian HBV carriers have been identified. The community-based REVEAL-HBV study illustrated the strong association between HBV-DNA level at study entry and risk of HCC over time, and male gender, older age, high serum alanine aminotransferase (ALT) level, positive HBeAg, higher HBV-DNA level, HBV genotype C infection and core promoter mutation are independently associated with a higher hepatocellular carcinoma (HCC) risk. Another hospital-based ERADICATE-B cohort further validated the HCC risk started to increase when HBV-DNA level was higher than 2,000 IU/mL. Of particular note, in patients with low viral load (HBV-DNA level <2,000 IU/mL), HBsAg level ≥1,000 IU/mL was a new independent risk factor for HCC. With the results from REVEAL-HBV study, a risk calculator for predicting HCC in adult non-cirrhotic patients has been developed and validated by independent international cohorts (REACH-B). With the combination of HBV-DNA, HBsAg, and ALT levels, ERADICATE-B study proposed an algorithm to predict disease progression and categorize risk levels of HCC as well as corresponding management in Asian HBV carriers. The introduction of transient elastography may further enhance the predictive power. In conclusion, HBsAg level can complement HBV-DNA level for the risk stratification of disease progression in Asian adult patients with chronic HBV infection.
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spelling doaj.art-b26289d745f34508b8ccbd3628befdce2022-12-21T22:22:17ZengKorean Association for the Study of the LiverClinical and Molecular Hepatology2287-27282287-285X2014-09-0120322322710.3350/cmh.2014.20.3.2231084Risk stratification of HBV infection in Asia-Pacific regionJia-Horng Kao0Department of Internal Medicine, National Taiwan University Hospital, Graduate Institute of Clinical Medicine, Hepatitis Research Center, and Department of Medical Research, National Taiwan University College of Medicine and National Taiwan University Hospital, Taipei, Taiwan.Hepatitis B virus (HBV) infection is the major etiology of chronic liver disease worldwide and thus a global health problem, especially in Asia-Pacific region. The long-term outcomes of Asian HBV carriers vary widely; however, a significant proportion of them will finally develop end-stage liver disease. Over the past decade, several host and HBV factors predictive of clinical outcomes in Asian HBV carriers have been identified. The community-based REVEAL-HBV study illustrated the strong association between HBV-DNA level at study entry and risk of HCC over time, and male gender, older age, high serum alanine aminotransferase (ALT) level, positive HBeAg, higher HBV-DNA level, HBV genotype C infection and core promoter mutation are independently associated with a higher hepatocellular carcinoma (HCC) risk. Another hospital-based ERADICATE-B cohort further validated the HCC risk started to increase when HBV-DNA level was higher than 2,000 IU/mL. Of particular note, in patients with low viral load (HBV-DNA level <2,000 IU/mL), HBsAg level ≥1,000 IU/mL was a new independent risk factor for HCC. With the results from REVEAL-HBV study, a risk calculator for predicting HCC in adult non-cirrhotic patients has been developed and validated by independent international cohorts (REACH-B). With the combination of HBV-DNA, HBsAg, and ALT levels, ERADICATE-B study proposed an algorithm to predict disease progression and categorize risk levels of HCC as well as corresponding management in Asian HBV carriers. The introduction of transient elastography may further enhance the predictive power. In conclusion, HBsAg level can complement HBV-DNA level for the risk stratification of disease progression in Asian adult patients with chronic HBV infection.http://e-cmh.org/upload/pdf/cmh-20-223.pdfHepatitis B virus (HBV)Hepatocellular carcinomaHBV-DNAHBsAgRisk stratification
spellingShingle Jia-Horng Kao
Risk stratification of HBV infection in Asia-Pacific region
Clinical and Molecular Hepatology
Hepatitis B virus (HBV)
Hepatocellular carcinoma
HBV-DNA
HBsAg
Risk stratification
title Risk stratification of HBV infection in Asia-Pacific region
title_full Risk stratification of HBV infection in Asia-Pacific region
title_fullStr Risk stratification of HBV infection in Asia-Pacific region
title_full_unstemmed Risk stratification of HBV infection in Asia-Pacific region
title_short Risk stratification of HBV infection in Asia-Pacific region
title_sort risk stratification of hbv infection in asia pacific region
topic Hepatitis B virus (HBV)
Hepatocellular carcinoma
HBV-DNA
HBsAg
Risk stratification
url http://e-cmh.org/upload/pdf/cmh-20-223.pdf
work_keys_str_mv AT jiahorngkao riskstratificationofhbvinfectioninasiapacificregion