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題名 New perspectives of biomarkers for the management of chronic hepatitis B
作者 Lin, Chih Lin
Kao, Jia Horng
貢獻者 心理系
關鍵詞 biological marker; cotransporter; hepatitis B surface antigen; hepatitis B(e) antigen; organic anion transporter; sodium-bile acid cotransporter; virus DNA; blood; complication; genetics; Hepatitis B virus; Hepatitis B, Chronic; human; liver cirrhosis; risk factor; single nucleotide polymorphism; Biomarkers; DNA, Viral; Hepatitis B e Antigens; Hepatitis B Surface Antigens; Hepatitis B virus; Hepatitis B, Chronic; Humans; Liver Cirrhosis; Organic Anion Transporters, Sodium-Dependent; Polymorphism, Single Nucleotide; Risk Factors; Symporters
日期 2016-12
上傳時間 15-Sep-2017 15:19:07 (UTC+8)
摘要 With recent advances in molecular and genomic investigations, the impact of hepatitis B viral and host factors on the progression of chronic HBV infection has been explored. For viral factors, hepatitis B viral load is a strong predictor for liver disease progression. Hepatitis B viral kinetics appear to be important for successful anti-viral therapy. Serum HBsAg level serves as a complementary marker to viral load for the prediction of HBV-related adverse outcomes in patients with low viral load. In those with low viral load, high serum HBsAg level is associated with higher risks of cirrhosis and HCC. Hepatitis B core-related antigen (HBcrAg) induces host immune responses, and the reduction of the HBcrAg level as well as the increment of total anti-HBc level are significantly associated with favorable outcomes. HBV genotypes (genotype C/D) and mutants (basal core promoter and deletion mutation in pre-S genes) are well known viral genetic markers to predict disease progression. For host factors, serum inflammatory biomarkers have been developed to evaluate the HBV-associated hepatic necroinflammation and fibrosis. Host single nucleotide polymorphism on sodium taurocholate cotransporting polypeptide (NTCP, an HBV entry receptor) may be associated with a decreased risk for cirrhosis and HCC. In conclusion, patients with chronic hepatitis B should be evaluated with relevant viral and host markers to identify those who are at a higher risk of liver disease progression and then receive timely antiviral therapy.
關聯 Clinical and molecular hepatology, 22(4), 423-431
資料類型 article
DOI http://dx.doi.org/10.3350/cmh.2016.0069
dc.contributor 心理系zh_TW
dc.creator (作者) Lin, Chih Linen_US
dc.creator (作者) Kao, Jia Horngen_US
dc.date (日期) 2016-12-
dc.date.accessioned 15-Sep-2017 15:19:07 (UTC+8)-
dc.date.available 15-Sep-2017 15:19:07 (UTC+8)-
dc.date.issued (上傳時間) 15-Sep-2017 15:19:07 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/113034-
dc.description.abstract (摘要) With recent advances in molecular and genomic investigations, the impact of hepatitis B viral and host factors on the progression of chronic HBV infection has been explored. For viral factors, hepatitis B viral load is a strong predictor for liver disease progression. Hepatitis B viral kinetics appear to be important for successful anti-viral therapy. Serum HBsAg level serves as a complementary marker to viral load for the prediction of HBV-related adverse outcomes in patients with low viral load. In those with low viral load, high serum HBsAg level is associated with higher risks of cirrhosis and HCC. Hepatitis B core-related antigen (HBcrAg) induces host immune responses, and the reduction of the HBcrAg level as well as the increment of total anti-HBc level are significantly associated with favorable outcomes. HBV genotypes (genotype C/D) and mutants (basal core promoter and deletion mutation in pre-S genes) are well known viral genetic markers to predict disease progression. For host factors, serum inflammatory biomarkers have been developed to evaluate the HBV-associated hepatic necroinflammation and fibrosis. Host single nucleotide polymorphism on sodium taurocholate cotransporting polypeptide (NTCP, an HBV entry receptor) may be associated with a decreased risk for cirrhosis and HCC. In conclusion, patients with chronic hepatitis B should be evaluated with relevant viral and host markers to identify those who are at a higher risk of liver disease progression and then receive timely antiviral therapy.en_US
dc.format.extent 766560 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Clinical and molecular hepatology, 22(4), 423-431en_US
dc.subject (關鍵詞) biological marker; cotransporter; hepatitis B surface antigen; hepatitis B(e) antigen; organic anion transporter; sodium-bile acid cotransporter; virus DNA; blood; complication; genetics; Hepatitis B virus; Hepatitis B, Chronic; human; liver cirrhosis; risk factor; single nucleotide polymorphism; Biomarkers; DNA, Viral; Hepatitis B e Antigens; Hepatitis B Surface Antigens; Hepatitis B virus; Hepatitis B, Chronic; Humans; Liver Cirrhosis; Organic Anion Transporters, Sodium-Dependent; Polymorphism, Single Nucleotide; Risk Factors; Symportersen_US
dc.title (題名) New perspectives of biomarkers for the management of chronic hepatitis Ben_US
dc.type (資料類型) article-
dc.identifier.doi (DOI) 10.3350/cmh.2016.0069-
dc.doi.uri (DOI) http://dx.doi.org/10.3350/cmh.2016.0069-