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首页> 外文期刊>The American Journal of Gastroenterology >Early HBeAg loss during peginterferon alpha-2b therapy predicts HBsAg loss: results of a long-term follow-up study in chronic hepatitis B patients.
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Early HBeAg loss during peginterferon alpha-2b therapy predicts HBsAg loss: results of a long-term follow-up study in chronic hepatitis B patients.

机译:聚乙二醇干扰素α-2b治疗期间早期HBeAg丢失可预测HBsAg丢失:这是对慢性乙型肝炎患者进行的长期随访研究的结果。

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OBJECTIVES: Treatment with pegylated interferon (PEG-IFN) alpha-2b results in hepatitis B e antigen (HBeAg) loss in 36% of patients at 6 months post treatment. The aim of this study was to determine whether a long-term response to PEG-IFN is dependent on the timing of HBeAg loss. METHODS: A total of 91 patients treated with PEG-IFN alpha-2b alone (100 microg per week) and 81 patients treated with PEG-IFN alpha-2b and lamivudine (100 mg/day) for 52 weeks were enrolled in this study. Patients were initially followed up at 4-week intervals and had one additional long-term follow-up (LTFU) visit (mean: 3.03+/-0.77 years 26 weeks post treatment). RESULTS: Of the 172 patients included, 78 patients (46%) did not have loss of HBeAg, 47 (27%) lost HBeAg within 32 weeks, and 47 patients (27%) had loss of HBeAg after week 32. At LTFU, patients with HBeAg loss< or =32 weeks had hepatitis B virus DNA of <400 copies/ml significantly more often than did those who lost HBeAg after week 32 (47 vs. 21%, respectively; P=0.009). Hepatitis B surface antigen (HBsAg) negativity was also observed significantly more often in patients with early HBeAg loss (36 vs. 4%, respectively, P<0.001). Early HBeAg loss tended to occur more often in patients treated with PEG-IFN and lamivudine combination therapy than in those treated with PEG-IFN alone (35 vs. 21%; P=0.10), as did HBsAg loss (15 vs. 8%; P=0.14). CONCLUSIONS: Early PEG-IFN-induced HBeAg loss results in a high likelihood of HBsAg loss and may be associated with more profound viral suppression during the first 32 weeks of therapy in patients treated with lamivudine combinations.
机译:目的:在治疗后6个月,使用聚乙二醇干扰素(PEG-IFN)α-2b治疗可导致36%的患者丧失乙肝e抗原(HBeAg)。这项研究的目的是确定对PEG-IFN的长期反应是否取决于HBeAg丢失的时间。方法:本研究共入选了91例接受PEG-IFNα-2b单独治疗(每周100微克)和81例接受PEG-IFNα-2b和拉米夫定(100毫克/天)治疗52周的患者。最初以4周为间隔对患者进行随访,并进行了另一次长期随访(LTFU)访问(平均:治疗后26周为3.03 +/- 0.77年)。结果:在172名患者中,有78名患者(46%)在32周内未丧失HBeAg,47名患者(27%)在32周内丧失了HBeAg,而47名患者(27%)在32周后丧失了HBeAg。 HBeAg丢失<或= 32周的患者比32周后丢失HBeAg的患者具有<400拷贝/ ml的乙型肝炎病毒DNA的频率明显更高(分别为47%对21%; P = 0.009)。在早期HBeAg丢失的患者中,乙肝表面抗原(HBsAg)阴性的发生率也更高(分别为36%和4%,P <0.001)。与单独使用PEG-IFN的患者相比,接受PEG-IFN和拉米夫定联合治疗的患者早期HBeAg丢失的发生率更高(35 vs. 21%; P = 0.10),HBsAg丢失的发生率也较高(15 vs. 8%)。 ; P = 0.14)。结论:拉米夫定联合治疗的患者在治疗的前32周内,早期PEG-IFN诱导的HBeAg丧失导致HBsAg丧失的可能性很高,并且可能与更深刻的病毒抑制有关。

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