學術產出-期刊論文

文章檢視/開啟

書目匯出

Google ScholarTM

政大圖書館

引文資訊

TAIR相關學術產出

題名 Perspectives and control of hepatitis B virus infection in Taiwan
作者 Lin, Chih-Lin;Kao, Jia-Horng
林志陵
貢獻者 心理系
關鍵詞 chronic hepatitis B;HBsAg;HBV DNA;HBV reactivation;hepatocellular carcinoma;risk calculator
日期 2015-10
上傳時間 3-十二月-2015 17:45:12 (UTC+8)
摘要 Hepatitis B virus (HBV) infection is endemic in Taiwan. After the implementation of universal hepatitis B vaccination, there was a significant reduction of hepatitis B surface antigen (HBsAg) seropositivity and HBV-related hepatocellular carcinoma (HCC) incidence in children, teenagers, and young adults. However, the incidence of HBV-related HCC in adults remains high. Through several community- and hospital-based cohort studies, the viral factors affecting the prognosis of HBV carriers have been illustrated. Serum HBV DNA level > 2000 IU/mL at study entry starts to increase the risks of cirrhosis and HCC in adult patients with chronic HBV infection. In addition, serum HBsAg level > 1000 IU/mL is associated with a higher risk of HCC in HBeAg-negative patients with low viral load. Virologically, HBV genotype C/D and core promote/pre-S mutations correlate with an increased HCC risk. Recently, a risk calculator has been developed to predict HCC in noncirrhotic patients with external validation. Therapeutically, hospital-based cohort and population-based nationwide studies indicated that interferon and nucleos(t)ide analogue treatments could reduce the incidence of HCC over time. Towards the ultimate goal of HBV eradication, several novel agents aiming at viral and host targets are under development. In addition, the immune therapy may play a key role in HBV cure in the foreseeable future.
關聯 Journal of the Formosan Medical Association, 114(10), 901-909
資料類型 article
DOI http://dx.doi.org/10.1016/j.jfma.2015.06.003
dc.contributor 心理系-
dc.creator (作者) Lin, Chih-Lin;Kao, Jia-Horng-
dc.creator (作者) 林志陵-
dc.date (日期) 2015-10-
dc.date.accessioned 3-十二月-2015 17:45:12 (UTC+8)-
dc.date.available 3-十二月-2015 17:45:12 (UTC+8)-
dc.date.issued (上傳時間) 3-十二月-2015 17:45:12 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/79581-
dc.description.abstract (摘要) Hepatitis B virus (HBV) infection is endemic in Taiwan. After the implementation of universal hepatitis B vaccination, there was a significant reduction of hepatitis B surface antigen (HBsAg) seropositivity and HBV-related hepatocellular carcinoma (HCC) incidence in children, teenagers, and young adults. However, the incidence of HBV-related HCC in adults remains high. Through several community- and hospital-based cohort studies, the viral factors affecting the prognosis of HBV carriers have been illustrated. Serum HBV DNA level > 2000 IU/mL at study entry starts to increase the risks of cirrhosis and HCC in adult patients with chronic HBV infection. In addition, serum HBsAg level > 1000 IU/mL is associated with a higher risk of HCC in HBeAg-negative patients with low viral load. Virologically, HBV genotype C/D and core promote/pre-S mutations correlate with an increased HCC risk. Recently, a risk calculator has been developed to predict HCC in noncirrhotic patients with external validation. Therapeutically, hospital-based cohort and population-based nationwide studies indicated that interferon and nucleos(t)ide analogue treatments could reduce the incidence of HCC over time. Towards the ultimate goal of HBV eradication, several novel agents aiming at viral and host targets are under development. In addition, the immune therapy may play a key role in HBV cure in the foreseeable future.-
dc.format.extent 525475 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Journal of the Formosan Medical Association, 114(10), 901-909-
dc.subject (關鍵詞) chronic hepatitis B;HBsAg;HBV DNA;HBV reactivation;hepatocellular carcinoma;risk calculator-
dc.title (題名) Perspectives and control of hepatitis B virus infection in Taiwan-
dc.type (資料類型) article-
dc.identifier.doi (DOI) 10.1016/j.jfma.2015.06.003-
dc.doi.uri (DOI) http://dx.doi.org/10.1016/j.jfma.2015.06.003-