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Early hepatitis B viral DNA clearance predicts treatment response at week 96

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 Hu...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413793/
https://www.ncbi.nlm.nih.gov/pubmed/28522916
http://dx.doi.org/10.3748/wjg.v23.i16.2978
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author 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
author_facet 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
author_sort Fu, Xiao-Yu
collection PubMed
description 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), 10-10(3) IU/mL (group 2), and > 10(3) 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 (10-10(3) 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 10-10(3) 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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spelling pubmed-54137932017-05-18 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 World J Gastroenterol Clinical Trials Study 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), 10-10(3) IU/mL (group 2), and > 10(3) 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 (10-10(3) 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 10-10(3) 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. Baishideng Publishing Group Inc 2017-04-28 2017-04-28 /pmc/articles/PMC5413793/ /pubmed/28522916 http://dx.doi.org/10.3748/wjg.v23.i16.2978 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Clinical Trials Study
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
Early hepatitis B viral DNA clearance predicts treatment response at week 96
title Early hepatitis B viral DNA clearance predicts treatment response at week 96
title_full Early hepatitis B viral DNA clearance predicts treatment response at week 96
title_fullStr Early hepatitis B viral DNA clearance predicts treatment response at week 96
title_full_unstemmed Early hepatitis B viral DNA clearance predicts treatment response at week 96
title_short Early hepatitis B viral DNA clearance predicts treatment response at week 96
title_sort early hepatitis b viral dna clearance predicts treatment response at week 96
topic Clinical Trials Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413793/
https://www.ncbi.nlm.nih.gov/pubmed/28522916
http://dx.doi.org/10.3748/wjg.v23.i16.2978
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