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Clinical significance of hepatitis B e antigen level easurement during long-term lamivudine therapy in chronic hepatitis B patients with e antigen positive

机译:长期拉米夫定治疗慢性乙型肝炎e抗原阳性患者中乙肝e抗原水平检测的临床意义

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摘要

AIM: To determine the changes of quantitative hepatitis B e antigen (HBeAg) that predicts early detection of non-response or breakthrough to long-term lamivudine (LAM) therapy.METHODS: Among HBeAg positive chronic hepatitis B patients who failed to achieve HBeAg seroconversion within 12 mo, we retrospectively analyzed 220 patients who had received LAM more than 24 mo.RESULTS: The mean duration of LAM therapy was 36 (range, 24-72) mo. HBeAg seroconversion after the first 12 mo of LAM therapy was achieved in 53 (24.1%) patients. Viral breakthrough was observed in 105 (47.7%) patients. To find out whether the changing patterns of HBeAg levels can predict the outcome of LAM therapy, we analyzed the reduction rates of HBeAg levels during LAM therapy. Using the decrease more than 90% of pretreatment HBeAg levels, the sensitivity and specificity of response were 96.2% and 70.1%, respectively. Patients were divided into 3 groups according to the reduction patterns of the decrease of quantitative HBeAg: decrescendo, decrescendo-crescendo, no change or fluctuating groups. The optimal time to predict non-response or breakthrough was the first 9 mo of therapy. At 9 mo of therapy, 49 (92.5%) of 53 patients who had achieved HBeAg seroconversion were included in the decrescendo group. On the contrary, in the no change or fluctuating group, only four (7.5%) had achieved HBeAg seroconversion. Among patients who did not show the continuous decrease of HBeAg levels at 9 mo, 95.2% (negative predictive value) failed to achieve HBeAg seroconversion.CONCLUSION: Almost all patients who failed to show a continuous decrease of HBeAg levels at 9 mo of LAM therapy were non-response or breakthrough. Therefore, monitoring changes of HBeAg levels during LAM therapy in HBeAg positive chronic hepatitis B may be valuable for identifying patients who are at high risk of non-response or breakthrough.
机译:目的:确定预测早期对长期拉米夫定(LAM)治疗无反应或突破的定量乙肝e抗原(HBeAg)的变化方法:在未能实现HBeAg血清转化的HBeAg阳性慢性乙肝患者中在12个月内,我们回顾性分析了220例接受LAM超过24个月的患者。结果:LAM治疗的平均持续时间为36(24-72)个月。在LAM治疗的前12个月中,有53名(24.1%)患者达到了HBeAg血清转化。在105(47.7%)位患者中观察到病毒突破。为了了解HBeAg水平的变化模式是否可以预测LAM治疗的结果,我们分析了LAM治疗期间HBeAg水平的降低率。使用减少超过90%的预处理HBeAg水平,反应的敏感性和特异性分别为96.2%和70.1%。根据定量HBeAg减少的减少方式将患者分为3组:逐渐减少,逐渐减少-逐渐增加,无变化或波动组。预测无反应或突破的最佳时间是治疗的前9个月。在治疗的9个月中,渐减组包括53例实现HBeAg血清转化的患者中的49例(92.5%)。相反,在无变化或波动的组中,只有四个(7.5%)达到了HBeAg血清转化。在9个月未显示HBeAg水平持续降低的患者中,有95.2%(阴性预测值)未能实现HBeAg血清转化。结论:几乎所有在LAM治疗9个月后未能显示HBeAg水平持续降低的患者没有回应或突破。因此,在HBeAg阳性慢性乙型肝炎的LAM治疗期间监测HBeAg水平的变化可能对识别无反应或突破的高风险患者有价值。

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