首页> 外文期刊>Journal of clinical gastroenterology >Change in serum hepatitis B surface antigen level and its clinical significance in treatment-naive, hepatitis B e antigen-positive patients receiving entecavir.
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Change in serum hepatitis B surface antigen level and its clinical significance in treatment-naive, hepatitis B e antigen-positive patients receiving entecavir.

机译:接受恩替卡韦治疗的初治乙肝e抗原阳性患者血清乙肝表面抗原水平的变化及其临床意义。

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BACKGROUND/AIM: We investigated changes in hepatitis B surface antigen (HBsAg) level and its correlation with clinical outcomes in treatment-naive chronic hepatitis B (CHB) patients undergoing entecavir therapy. PATIENTS AND METHODS: Among 51 hepatitis B e antigen (HBeAg)-positive treatment-naive CHB patients receiving entecavir for more than 1 year, 28 were enrolled. HBsAg levels were measured at baseline, 6 months, and 12 months after treatment using the Architect HBsAg QT assay (Abbott, dynamic; range: 0.05 to 125,000 IU/mL). Serum alanine aminotransferase, HBeAg, anti-HBe, and hepatitis B virus (HBV) DNA (Cobas Taqman: low detection limit 1.84 log10 copies/mL) were measured at baseline and every 3 months. The HBsAg response was defined as an HBsAg level that decreased more than 1 log10 IU/mL from baseline level at 12 months after entecavir treatment. RESULTS: Twenty-eight patients were treated for a median period of 21 months (range: 18 to 24 mo). Serum HBsAg level showed a mean of 4.0, 3.7, and 3.6 log10 IU/mL at pretreatment, 6, and 12 months, respectively, and declined significantly (P<0.001). Serum HBV DNA level showed a mean of 8.1, 3.1, and 2.4 log10 copies/mL at pretreatment, 6, and 12 months, respectively, and declined significantly (P<0.001). The decline in HBsAg level was significantly correlated with that of the HBV DNA level at 12 months from baseline (gamma=0.391, P=0.044). Five patients showed an HBsAg response, and cumulative incidence of HBeAg loss at 1 year after entecavir treatment was 80% versus 30% in patients with an HBsAg response and those without, respectively (P=0.034). CONCLUSIONS: Monitoring changes in quantitative HBsAg level could be a useful parameter for assessing the response to entecavir therapy in HBeAg-positive treatment-naive CHB patients.
机译:背景/目的:我们调查了接受恩替卡韦治疗的未经治疗的慢性乙型肝炎(CHB)患者中乙型肝炎表面抗原(HBsAg)水平的变化及其与临床结局的相关性。患者和方法:在接受恩替卡韦治疗1年以上的51例未接受乙肝e抗原(HBeAg)阳性治疗的慢性乙肝患者中,有28例入选。使用Architect HBsAg QT分析法(Abbott,动态;范围:0.05至125,000 IU / mL)在治疗的基线,治疗后6个月和12个月测量HBsAg水平。在基线和每3个月测量一次血清丙氨酸氨基转移酶,HBeAg,抗HBe和乙型肝炎病毒(HBV)DNA(Cobas Taqman:低检测限1.84 log10拷贝/ mL)。 HBsAg反应定义为在恩替卡韦治疗后12个月,HBsAg水平从基线水平下降超过1 log10 IU / mL。结果:28名患者接受了21个月的中位治疗(范围:18至24 mo)。血清HBsAg水平在预处理,第6和12个月时分别显示为4.0、3.7和3.6 log10 IU / mL,并且显着下降(P <0.001)。血清HBV DNA水平在预处理,分别为6和12个月时分别显示分别为8.1、3.1和2.4 log10个拷贝/ mL,并且显着下降(P <0.001)。从基线开始的12个月,HBsAg水平的下降与HBV DNA水平的下降显着相关(γ= 0.391,P = 0.044)。五例患者表现出HBsAg应答,恩替卡韦治疗1年后,HBeAg丢失的累积发生率分别为80%和HBsAg应答患者分别为30%(P = 0.034)。结论:监测HBsAg定量水平的变化可能是评估未接受HBeAg阳性的CHB患者对恩替卡韦治疗反应的有用参数。

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