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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Impact of hepatitis C and liver fibrosis on antiretroviral plasma drug concentrations in HIV-HCV co-infected patients: the HEPADOSE study.
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Impact of hepatitis C and liver fibrosis on antiretroviral plasma drug concentrations in HIV-HCV co-infected patients: the HEPADOSE study.

机译:丙型肝炎和肝纤维化对HIV-HCV合并感染患者抗逆转录病毒血浆药物浓度的影响:HEPADOSE研究。

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摘要

OBJECTIVES: To compare plasma antiretroviral concentrations in HIV-HCV co-infected and in matched HIV mono-infected patients. METHODS: This was a cross-sectional, observational study. Antiretroviral trough concentrations (C(min)) in plasma were measured in HIV-HCV co-infected patients with liver disease documented by liver biopsy, matched with HIV mono-infected patients according to gender and antiretroviral treatment. C(min) values in serum were measured using an HPLC method. Statistical analysis was performed using the Wilcoxon test. RESULTS: Seventy-three HIV-HCV co-infected patients and 66 HIV-infected patients were enrolled; 70% of patients were receiving a protease inhibitor (PI)- and 30% a non-nucleoside reverse transcriptase inhibitor (NNRTI)-based regimen. Among the 73 co-infected patients, 27 had a fibrosis score (Fibrotest((R))) of F4. Abacavir was the only nucleoside reverse transcriptase inhibitor whose trough concentrations differed between the co-infected and mono-infected groups. PI median plasma C(min) values were not different in the two groups, except for lopinavir, with a lower C(min) in the co-infected group than in the HIV-infected group (median 3673 versus 5990 ng/mL, P=0.04), and nelfinavir, with significantly higher concentrations in the co-infected group. Seventy-five percent of co-infected patients scoring F4, 33% of those scoring F0-F3 and 12% of HIV-infected patients were underdosed (P=0.02). Co-infected patients receiving an NNRTI had a higher plasma C(min) than HIV-infected patients; median C(min) was 3583 versus 1494 ng/mL (P=0.025) and 5331 versus 3954 ng/mL (P=0.10) for efavirenz and nevirapine, respectively. Overall, there was a greater proportion of co-infected patients with high concentrations of both NNRTIs (15/23) compared with HIV mono-infected patients (5/21) (P=0.008), especially in co-infected patients with an advanced liver fibrosis stage. CONCLUSIONS: Median plasma C(min) values differed significantly between HIV and HIV-HCV co-infected patients for abacavir, lopinavir and efavirenz. NNRTIs were strongly overdosed in HIV-HCV co-infected patients.
机译:目的:比较合并感染的HIV-HCV和匹配的HIV单一感染患者的血浆抗逆转录病毒浓度。方法:这是一项横断面观察研究。在通过肝活检证实的HIV-HCV合并感染的肝病患者中,测量了血浆中的抗逆转录病毒谷浓度(C(min)),并根据性别和抗逆转录病毒疗法与HIV单感染的患者相匹配。使用HPLC方法测量血清中的C(min)值。使用Wilcoxon检验进行统计分析。结果:纳入73例HIV-HCV合并感染患者和66例HIV感染患者。 70%的患者正在接受蛋白酶抑制剂(PI)-治疗,而30%的患者正在接受基于非核苷逆转录酶抑制剂(NNRTI)的治疗方案。在73例合并感染的患者中,有27例的纤维化评分为(Fibrotest(R))为F4。阿巴卡韦是唯一的一种核苷类逆转录酶抑制剂,其共同感染组和单一感染组之间的谷浓度不同。除洛匹那韦外,两组的PI中值血浆C(min)值均无差异,共同感染组的C(min)低于HIV感染组(中位数3673对5990 ng / mL,P = 0.04)和奈非那韦(nelfinavir),在共同感染组中的浓度明显较高。服用F4的合并感染患者中有75%,服用F0-F3的患者中33%和感染HIV的患者中有12%的剂量不足(P = 0.02)。接受NNRTI的合并感染患者的血浆C(min)高于HIV感染患者;依非韦伦和奈韦拉平的中位C(min)分别为3583对1494 ng / mL(P = 0.025)和5331对3954 ng / mL(P = 0.10)。总体而言,与HIV单感染患者(5/21)相比,两种NNRTIs高浓度的合并感染患者(15/23)的比例更高(P = 0.008),特别是在晚期合并感染的患者中肝纤维化阶段。结论:HIV和HIV-HCV合并感染的阿巴卡韦,洛匹那韦和依非韦伦的血浆中值C(min)值存在显着差异。在HIV-HCV合并感染的患者中,NNRTIs的剂量严重过量。

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