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Comparison of the 48-week efficacy between entecavir and adefovir in HBeAg-positive nucleos(t)ide-na?ve Asian patients with chronic hepatitis B: a meta-analysis

机译:恩替卡韦和阿德福韦在亚洲慢性乙型肝炎HBeAg阳性初治亚洲患者中48周疗效的比较:一项荟萃分析

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Background Although entacavir and adefovir were widely used in most Asian countries, there were few conclusions drawn from a meta-analysis for comparing the efficacy between entecavir and adefovir in nucleos(t)ide-na?ve Asian patients with chronic hepatitis B (CHB). The aim of this study was to evaluate the 48-week efficacy between the two drugs in HBeAg-positive nucleos(t)ide-na?ve Asian CHB patients with the method of Meta analysis, which was generally accepted by the international as the best evidence for evaluating the efficacy of drugs. Methods We searched all data documented in Pubmed, Embase, Wanfang Database and CNKI (China National Knowledge Infrastructure) before November 30, 2010. Heterogeneity was examined by Chi-square test, the relative risk calculated and forest plot drawn. Rates of undetected serum HBV DNA, serum alanine aminotransferase (ALT) normalization, HBeAg clearance and HBeAg seroconversion were analyzed. A total of 6 articles was included. Meta analysis showed that the rate of undetected serum HBV DNA (relative risk, 1.73; 95% confidence interval, 1.38-2.17; P P = 0.009) in the entecavir group were higher than those in the adefovir group. However, no statistic significance existed between the two groups in the rate of HBeAg clearance (relative risk, 0.77; 95% confidence interval, 0.44-1.35; P = 0.36), or the rate of HBeAg seroconversion (relative risk, 0.74; 95% confidence interval, 0.28-1.94; P = 0.53). Conclusions Entecavir is superior to adefovir in decreasing serum HBV DNA and normalizing ALT but similar with adefovir in clearing HBeAg and encouraging HBeAg seroconversion for the HBeAg-positive nucleos(t)ide-naive Asian patients with chronic hepatitis B. Adefovir can be still used for first-line therapy in these patients.
机译:背景:尽管恩替卡韦和阿德福韦在大多数亚洲国家被广泛使用,但根据荟萃分析得出的结论很少用于比较恩替卡韦和阿德福韦在未接受过核苷酸治疗的亚洲初治慢性乙型肝炎(CHB)患者中的疗效。 。这项研究的目的是通过Meta分析方法评估这两种药物在HBeAg阳性未确诊的亚洲CHB患者中的48周疗效,这是国际上公认的最佳方法评估药物功效的证据。方法我们在2010年11月30日之前检索了Pubmed,Embase,Wanfang数据库和CNKI(中国国家知识基础设施)中记录的所有数据。通过卡方检验检查异质性,计算相对风险并绘制森林图。分析未检出血清HBV DNA,血清丙氨酸氨基转移酶(ALT)正常化,HBeAg清除率和HBeAg血清转化率。总共包括6条文章。荟萃分析显示,恩替卡韦组未检出血清HBV DNA的发生率(相对危险度为1.73; 95%置信区间为1.38-2.17; P P = 0.009)高于阿德福韦组。但是,两组之间在HBeAg清除率(相对危险度,0.77; 95%置信区间,0.44-1.35; P = 0.36)或HBeAg血清转化率(相对危险度,0.74; 95%)之间没有统计学意义。置信区间为0.28-1.94; P = 0.53)。结论恩替卡韦在降低血清HBV DNA和使ALT正常化方面优于阿德福韦,但与阿德福韦相似,在亚洲慢性乙型肝炎患者中,HBeAg阳性核苷(t)初治患者清除HBeAg和鼓励HBeAg血清转化。阿德福韦仍可用于这些患者的一线治疗。

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