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接受聚乙二醇干扰素 α-2a 联合利巴韦林治疗乙型和丙型肝炎病毒双重慢性感染患者的 HBsAg 特征。

HBsAg profiles in patients receiving peginterferon alfa-2a plus ribavirin for the treatment of dual chronic infection with hepatitis B and C viruses.

机构信息

Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

J Infect Dis. 2010 Jul 1;202(1):86-92. doi: 10.1086/653209.

Abstract

BACKGROUND

With use of peginterferon alfa-2a and ribavirin combination therapy in patients with dual chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, 11.2% of patients achieved clearance of hepatitis B surface antigen (HBsAg) at 6 months after treatment; however, reactivation of HBV DNA was observed in 36.3%. We investigated the predictive potential of HBsAg quantification.

METHODS

HBsAg quantification was performed in 120 e antigen-negative patients dually infected with HBV and hepatitis C virus and treated with peginterferon alfa-2a/ribavirin for 48 weeks (HCV genotype 1; n = 74) or 24 weeks (HCV genotype 2/3; n = 46). HBsAg was quantified at baseline, week 4, week 12, end of treatment, and 24 weeks after treatment.

RESULTS

The baseline median serum HBsAg level was 120 IU/mL and decreased gradually during treatment. Low baseline HBsAg was significantly associated with HBsAg clearance (40% for HBsAg level 20 IU/mL vs 2.2% for HBsAg level >20 IU/mL; P < .05). A decrease in HBsAg level from baseline to week 12 of 50% was associated with a reduced likelihood of HBV DNA reactivation in patients with baseline undetectable serum HBV DNA (positive predictive value, 89.5%).

CONCLUSIONS

HBsAg quantification appears to be a useful indicator of posttreatment outcome in patients dually infected with HBV and hepatitis C virus.

摘要

背景

在接受聚乙二醇干扰素 alfa-2a 和利巴韦林联合治疗的双重慢性乙型肝炎病毒 (HBV) 和丙型肝炎病毒 (HCV) 感染患者中,有 11.2%的患者在治疗后 6 个月时清除了乙型肝炎表面抗原 (HBsAg);然而,有 36.3%的患者观察到 HBV DNA 再激活。我们研究了 HBsAg 定量的预测潜力。

方法

对 120 例 e 抗原阴性的 HBV 和 HCV 双重感染患者进行 HBsAg 定量检测,这些患者接受聚乙二醇干扰素 alfa-2a/利巴韦林治疗 48 周(HCV 基因型 1;n = 74)或 24 周(HCV 基因型 2/3;n = 46)。在基线、第 4 周、第 12 周、治疗结束时和治疗结束后 24 周检测 HBsAg。

结果

基线时血清 HBsAg 中位数为 120 IU/mL,治疗期间逐渐下降。低基线 HBsAg 与 HBsAg 清除显著相关(HBsAg 水平 20 IU/mL 时为 40%,HBsAg 水平 >20 IU/mL 时为 2.2%;P <.05)。从基线到第 12 周 HBsAg 水平下降 50%与基线时血清 HBV DNA 不可检测的患者 HBV DNA 再激活可能性降低相关(阳性预测值,89.5%)。

结论

HBsAg 定量似乎是预测 HBV 和 HCV 双重感染患者治疗后结局的有用指标。

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