Lee Shou-Wu, Lee Teng-Yu, Yang Sheng-Shun, Peng Yen-Chun, Yeh Hong-Zen, Chang Chi-Sen
Division of Gastroenterology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan, Republic of China.
Department of Internal Medicine, Chung Shan Medical University, Taichung, Taiwan, Republic of China.
Gastroenterology Res. 2018 Apr;11(2):124-129. doi: 10.14740/gr971w. Epub 2018 Apr 7.
Clearance of hepatitis C virus (HCV) has been reported to induce the reactivation of hepatitis B virus (HBV). The aim of this study was to investigate the rate of HBV reactivation in HCV-infected Chinese patients who received treatment with pan-oral direct-acting antivirals (DAAs).
Data from HCV subjects receiving oral DAA therapy were retrospectively collected from October 2015 to May 2017. Patients who were seropositive for HBsAg or anti-HBc were enrolled. The efficacy of DAAs, including end-of-treatment virologic response (ETVR) and sustained virologic response (SVR) 12, was recorded. HBV virologic reactivation was defined as a reappearance of HBsAg, or increased HBV DNA by at least one log IU/mL. HBV clinical reactivation was defined as virologic reactivation and serum alanine aminotransferase (ALT) over two-fold of the upper limit of normal.
There were 11 (7.2%) cases and 53 (34.6%) cases in the HBsAg group and the anti-HBc group among all 153 subjects. All individuals achieved ETVR and SVR12. There were no cases with reappearance of HBsAg during DAAs therapy. Among seven cases in the HBsAg group whose HBV DNA level was determined, HBV virological reactivation was detected in two subjects (28.6%). Among all 11 subjects in the HBsAg group, there was one (9.1%) case with HBV clinical reactivation, which was resolved following treatment with Entaclavir. The case with HBV clinical reactivation had a higher baseline HBV DNA viral load (1,380 IU/mL) compared with that of the other patients (20 - 296 IU/mL).
HBV virological and clinical reactivation occurred in 28.5% and 9.1% of subjects with HBsAg seropositivity. No HBV reactivation was observed in the cases with past HBV infection.
据报道,丙型肝炎病毒(HCV)清除可诱导乙型肝炎病毒(HBV)再激活。本研究旨在调查接受全口服直接抗病毒药物(DAA)治疗的HCV感染中国患者中HBV再激活的发生率。
回顾性收集2015年10月至2017年5月接受口服DAA治疗的HCV患者的数据。纳入HBsAg或抗-HBc血清学阳性的患者。记录DAA的疗效,包括治疗结束时病毒学应答(ETVR)和持续病毒学应答(SVR)12。HBV病毒学再激活定义为HBsAg再现,或HBV DNA增加至少一个对数IU/mL。HBV临床再激活定义为病毒学再激活且血清丙氨酸氨基转移酶(ALT)超过正常上限的两倍。
在所有153名受试者中,HBsAg组有11例(7.2%),抗-HBc组有53例(34.6%)。所有个体均实现了ETVR和SVR12。DAA治疗期间无HBsAg再现的病例。在HBsAg组中检测HBV DNA水平的7例患者中,2例(28.6%)检测到HBV病毒学再激活。在HBsAg组的所有11名受试者中,有1例(9.1%)发生HBV临床再激活,恩替卡韦治疗后病情缓解。与其他患者(20 - 296 IU/mL)相比,发生HBV临床再激活的患者基线HBV DNA病毒载量更高(1380 IU/mL)。
HBsAg血清学阳性的受试者中,HBV病毒学和临床再激活的发生率分别为28.5%和9.1%。既往HBV感染患者未观察到HBV再激活。