首页> 外文期刊>Alimentary pharmacology & therapeutics. >Pharmacodynamics of peginterferon alpha-2a and peginterferon alpha-2b in interferon-naive patients with chronic hepatitis C: a randomized, controlled study.
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Pharmacodynamics of peginterferon alpha-2a and peginterferon alpha-2b in interferon-naive patients with chronic hepatitis C: a randomized, controlled study.

机译:聚乙二醇干扰素α-2a和聚乙二醇干扰素α-2b在无干扰素的慢性丙型肝炎患者中的药效学:一项随机对照研究。

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BACKGROUND: Peginterferon alpha-2a and alpha-2b, the two commercially available pegylated interferons, have different pharmacokinetic properties that produce differing abilities to suppress replication of the hepatitis C virus. AIM: To compare the pharmacodynamics of peginterferon alpha-2a and peginterferon alpha-2b in interferon-naive patients with chronic hepatitis C. METHODS: Patients were randomized to receive peginterferon alpha-2a, 180 microg (n = 10) or peginterferon alpha-2b 1.0 microg/kg (n = 12) once weekly. The enzymatic activity of 2'5'-oligoadenylate synthetase and levels of neopterin and beta(2)-microglobulin were measured at baseline and at 24, 48, 120 and 168 h. RESULTS: Oligoadenylate synthetase activity and serum neopterin and beta(2)-microglobulin concentrations did not differ significantly between the two patient groups at any time point, nor was there a significant correlation between the serum area under the concentration-time curve of either peginterferon and the area under the concentration-time curve for 2',5'-oligoadenylate synthetase, neopterin and beta(2)-microglobulin. The area under the concentration-time curves calculated for these three markers did not correlate with body mass index stratified at <25 and >or=25 kg/m(2) for either peginterferon. CONCLUSIONS: Despite pharmacokinetic differences between peginterferon alpha-2a and peginterferon alpha-2b, the pharmacodynamic profiles of the two formulations appear to be comparable.
机译:背景:聚乙二醇化干扰素α-2a和α-2b,这两种市售的聚乙二醇化干扰素,具有不同的药代动力学特性,可产生不同的抑制丙型肝炎病毒复制的能力。目的:比较聚乙二醇干扰素α-2a和聚乙二醇干扰素α-2b在初治慢性丙型肝炎患者中的药效学。每周一次,每次1.0 microg / kg(n = 12)。在基线,24、48、120和168小时测量2'5'-寡腺苷酸合成酶的酶活性以及新蝶呤和β(2)-微球蛋白的水平。结果:两组患者在任何时间点的寡腺苷酸合成酶活性,血清新蝶呤和β(2)-微球蛋白浓度均无显着差异,在聚乙二醇干扰素和聚乙二醇干扰素的浓度-时间曲线下,血清面积之间也无显着相关性。 2',5'-寡腺苷酸合成酶,新蝶呤和β(2)-微球蛋白浓度-时间曲线下的面积。对于这三种聚乙二醇干扰素,针对这三个标记物计算出的浓度-时间曲线下的面积与在<25和>或= 25 kg / m(2)时分层的体重指数不相关。结论:尽管聚乙二醇干扰素α-2a和聚乙二醇干扰素α-2b之间的药代动力学差异,但两种制剂的药效学特征似乎是可比的。

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