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首页> 外文期刊>Infection and Drug Resistance >Comparison of pegylated interferon monotherapy and de novo pegylated interferon plus tenofovir combination therapy in patients with chronic hepatitis B
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Comparison of pegylated interferon monotherapy and de novo pegylated interferon plus tenofovir combination therapy in patients with chronic hepatitis B

机译:聚乙二醇干扰素单药治疗与从头聚乙二醇干扰素联合替诺福韦治疗慢性乙型肝炎的比较

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Background and aim: We aimed to evaluate the effectiveness of pegylated interferon (Peg-IFN) monotherapy (IFN group) and combination therapy with tenofovir (TDF) and Peg-IFN (IFN+TDF group) in chronic hepatitis B (CHB) patients. Patients and methods: Data of 143 CHB patients were analyzed in this study. All patients enrolled received liver biopsy. Virologic responses were defined as hepatitis B virus (HBV) DNA 100 IU/mL, biochemical responses were defined as normalization?of alanine aminotransferse (ALT) levels, and HBeAg serological response was defined as HBeAg loss or HBeAg seroconversion to HBeAb. HBsAg serological response was?defined as HBsAg loss or HBsAg seroconversion to HBsAb. Results: We observed that a total of 16.7% (11/66) and 33.8% (26/77) patients in IFN and IFN+TDF group achieved complete viral suppression after 48 weeks treatment ( P =0.02). Although HBeAg levels in CHB patients in the IFN+TDF group decreased more rapidly during the 48-week treatment, we did not observe significant differences in HBeAg serological loss or seroconversion rates between the two groups at 24 and 48 weeks. HBsAg loss was observed in 13.0% (10/77) of CHB patients in the IFN+TDF group at 48 weeks, compared with only 3% (2/66) patients in the IFN group ( P =0.032). No significant difference was observed in HBsAg seroconversion rate between the two groups during 48-week treatment. The biochemical response rate was also significantly higher in the IFN+TDF group than that in the IFN group at week 48 ( P =0.015). Multivariate logistic analysis showed that IFN+TDF treatment (OR=4.41, P =0.003), severe baseline hepatic inflammation (OR=4.16, P 0.001), and lower baseline serum HBV DNA levels (OR=0.98, P =0.03) were strong predictors for the virological response. Younger age (OR=0.89, P =0.01), higher baseline ALT level (OR=1.01, P =0.038), and lower baseline HBeAg level (OR=0.99, P =0.008) were independent predictors for HBeAg sero-response after 48 weeks treatment. While only severe liver fibrosis (OR=1.69, P =0.028) and lower baseline HBsAg level (OR=0.22, P =0.005) were independent factors associated with HBsAg sero-response after 48 weeks treatment. Conclusion: Peg-IFN combined with TDF may increase the virological response rate, biochemical response rate, and HBsAg loss rate in patients with CHB infection. The combination treatment is more suitable for those patients who are likely to respond to the treatment.
机译:背景与目的:我们旨在评估聚乙二醇干扰素(Peg-IFN)单药治疗(IFN组)和替诺福韦(TDF)和Peg-IFN(IFN + TDF组)联合治疗对慢性乙型肝炎(CHB)患者的有效性。患者和方法:本研究分析了143例CHB患者的数据。所有入组患者均接受了肝活检。病毒学应答定义为<100 IU / mL的乙型肝炎病毒(HBV)DNA,生化应答定义为丙氨酸氨基转移(ALT)水平的正常化,HBeAg血清应答定义为HBeAg丧失或HBeAg血清转化为HBeAb。 HBsAg血清学反应定义为HBsAg丧失或HBsAg血清转化为HBsAb。结果:我们观察到在治疗48周后,IFN和IFN + TDF组中分别有16.7%(11/66)和33.8%(26/77)的患者实现了完全的病毒抑制(P = 0.02)。尽管在48周的治疗期间,IFN + TDF组的CHB患者中的HBeAg水平下降得更快,但我们在24和48周时没有观察到两组之间的HBeAg血清学丧失或血清转化率有显着差异。在第48周,在IFN + TDF组的CHB患者中观察到HBsAg丢失,占13.0%(10/77),而在IFN组中只有3%(2/66)患者(P = 0.032)。在48周的治疗期间,两组之间的HBsAg血清转化率没有显着差异。在第48周时,IFN + TDF组的生化反应率也显着高于IFN组(P = 0.015)。多因素logistic分析表明,IFN + TDF治疗(OR = 4.41,P = 0.003),严重基线肝炎(OR = 4.16,P <0.001)和基线HBV DNA水平较低(OR = 0.98,P = 0.03)病毒学应答的强预测因子。年龄较小(OR = 0.89,P = 0.01),基线ALT水平较高(OR = 1.01,P = 0.038)和基线HBeAg水平较低(OR = 0.99,P = 0.008)是48岁后HBeAg血清反应的独立预测因子。周治疗。尽管只有严重的肝纤维化(OR = 1.69,P = 0.028)和基线HBsAg水平降低(OR = 0.22,P = 0.005)是治疗48周后与HBsAg血清反应相关的独立因素。结论:Peg-IFN联合TDF可提高CHB感染患者的病毒学应答率,生化应答率和HBsAg丢失率。联合治疗更适合那些可能对治疗有反应的患者。

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