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Early hepatitis B viral DNA clearance predicts treatment response at week 96.
Fu, Xiao-Yu; Tan, De-Ming; Liu, Cui-Mei; Gu, Bin; Hu, Li-Hua; Peng, Zhong-Tian; Chen, Bin; Xie, Yuan-Lin; Gong, Huan-Yu; Hu, Xiao-Xuan; Yao, Lian-Hui; Xu, Xiao-Ping; Fu, Zheng-Yuan; He, Lang-Qiu; Li, Si-Hai; Long, Yun-Zhu; Li, De-Hui; Gu, Ji-Long; Peng, Shi-Fang.
Afiliação
  • Fu XY; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Tan DM; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Liu CM; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Gu B; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Hu LH; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Peng ZT; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Chen B; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Xie YL; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Gong HY; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Hu XX; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Yao LH; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Xu XP; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Fu ZY; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • He LQ; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Li SH; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Long YZ; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Li DH; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Gu JL; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
  • Peng SF; Xiao-Yu Fu, De-Ming Tan, Cui-Mei Liu, Shi-Fang Peng, Key Laboratory of Viral Hepatitis, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.
World J Gastroenterol ; 23(16): 2978-2986, 2017 Apr 28.
Article em En | MEDLINE | ID: mdl-28522916
ABSTRACT

AIM:

To investigate whether hepatitis viral DNA load at 24 wk of treatment predicts response at 96 wk in patients with chronic hepatitis B.

METHODS:

A total of 172 hepatitis B envelope antigen (HBeAg)-positive chronic hepatitis B patients who received initial treatment at 16 tertiary hospitals in Hunan Province, China were enrolled in this study. All patients received conventional doses of lamivudine and adefovir dipivoxil, telbivudine, entecavir dispersible tablets, or entecavir tablets for 96 wk. Patients who used other antiviral drugs or antitumor and immune regulation therapy were excluded. Patients were stratified into three groups according to their viral DNA load at 24 wk < 10 IU/mL (group 1), 10-103 IU/mL (group 2), and > 103 IU/mL (group 3). Correlations of 24-wk DNA load with HBeAg negative status and HBeAg seroconversion at 96 wk were analyzed. Receiver operating characteristic curve analysis was used to test the predictive value of the HBV DNA load at 24 wk for long-term response.

RESULTS:

The rates of conversion to HBeAg negative status and HBeAg seroconversion rates were 53.7% and 51.9%, respectively, in group 1; 35.21% and 32.39% in group 2; and 6.38% and 6.38% in group 3. The receiver operating characteristic curves for the three subgroups revealed that the lowest DNA load (< 10 IU/mL) was better correlated with response at 96 wk than a higher DNA load (10-103 IU/mL). Nested PCR was used for amplifying and sequencing viral DNA in patients with a viral DNA load > 200 IU/mL at 96 wk; resistance mutations involving different loci were present in 26 patients, and three of these patients had a viral DNA load 10-103 IU/mL at 96 wk.

CONCLUSION:

Hepatitis B viral DNA load at 24 wk of antiviral treatment in patients with chronic hepatitis B is a predictor of the viral load and response rate at 96 wk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / DNA Viral / Vírus da Hepatite B / Hepatite B Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: World J Gastroenterol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / DNA Viral / Vírus da Hepatite B / Hepatite B Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: World J Gastroenterol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China