首页> 美国卫生研究院文献>World Journal of Gastroenterology >Antiviral efficacy of adefovir dipivoxil versus lamivudine in patients with chronic hepatitis B sequentially treated with lamivudine and adefovir due to lamivudine resistance
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Antiviral efficacy of adefovir dipivoxil versus lamivudine in patients with chronic hepatitis B sequentially treated with lamivudine and adefovir due to lamivudine resistance

机译:拉米夫定和阿德福韦因拉米夫定耐药性而导致的慢性乙型肝炎患者使用阿德福韦酯与拉米夫定的抗病毒疗效

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摘要

AIM: To compare the antiviral efficacy of adefovir (ADV) in lamivudine (LMV)-resistant patients with LMV treatment in nucleoside-naïve patients, using serum samples collected sequentially during the course of treatment progressing from LMV to ADV.METHODS: Forty-four patients with chronic hepatitis B (CHB) were included. The patients were initially treated with LMV and then switched to ADV when LMV resistance developed. Antiviral efficacy was assessed by measuring the following: reduction in serum HBV DNA from baseline, HBV DNA negative conversion (defined as HBV DNA being undectable by the hybridization assay), and HBV DNA response (either HBV DNA level ≤ 105 copies/mL or a ≥ 2 log10 reduction from baseline HBV DNA level).RESULTS: After two and six months of treatment, HBV DNA reduction was greater with LMV compared to ADV treatment (P = 0.021). HBV DNA negative conversion rates were 64% and 27% after one month of LMV and ADV treatment respectively (P = 0.001). Similarly, HBV DNA response rates were 74% and 51% after two months of LMV and ADV treatment respectively (P = 0.026).The time taken to HBV DNA negative conversion and to HBV DNA response were both delayed in ADV treatment compared with LMV.CONCLUSION: The antiviral efficacy of ADV in LMV-resistant patients is slower and less potent than that with LMV in nucleoside-naïve patients during the early course of treatment.
机译:目的:使用从LMV到ADV的治疗过程中依次收集的血清样本,比较阿德福韦(ADV)对未接受拉米夫定(LMV)的LMV治疗的核苷初治患者的抗病毒疗效。包括慢性乙型肝炎(CHB)患者。患者最初接受LMV治疗,然后在LMV耐药性发展时转为ADV。通过测量以下各项来评估抗病毒功效:血清HBV DNA从基线水平降低,HBV DNA负转化(定义为杂交试验无法确定的HBV DNA)和HBV DNA反应(HBV DNA水平≤10 5 < / sup>拷贝/ mL或从基线HBV DNA水平降低≥2 log10。结果:治疗2个月和6个月后,与ADV治疗相比,LMV的HBV DNA降低更大(P = 0.021)。 LMV和ADV治疗一个月后,HBV DNA阴性转化率分别为64%和27%(P = 0.001)。同样,LMV和ADV治疗两个月后HBV DNA应答率分别为74%和51%(P = 0.026)。与LMV相比,ADV治疗中HBV DNA阴性转化和HBV DNA响应时间均被延迟。结论:在早期治疗过程中,LMV耐药患者中ADV的抗病毒作用比未使用核苷的患者中LMV的抗病毒作用慢,效力低。

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