Impact of hepatitis C and liver fibrosis on antiretroviral plasma drug concentrations in HIV-HCV co-infected patients: the HEPADOSE study

被引:13
作者
Dominguez, Stephanie [1 ]
Ghosn, Jade [1 ]
Peytavin, Gilles [3 ]
Guiguet, Marguerite
Tubiana, Roland [1 ]
Valantin, Marc Antoine [1 ]
Murphy, Robert [1 ]
Bricaire, Francois [1 ]
Benhamou, Yves [2 ]
Katlama, Christine [1 ]
机构
[1] CHU Pitie Salpetriere, AP HP, Dept Malad Infect & Trop, INSERM U720, Paris, France
[2] CHU Pitie Salpetriere, AP HP, Dept Hepatogastroenterol, Paris, France
[3] CHU Bichat Cluade Bernard, AP HP, Lab Pharmacol Clin, Paris, France
关键词
HIV; chronic hepatitis C; therapeutic drug monitoring; liver disease; safety; toxicity; antiretroviral therapy; pharmacology; HUMAN-IMMUNODEFICIENCY-VIRUS; COINFECTED SUBJECTS; PROTEASE INHIBITOR; EFAVIRENZ-THERAPY; HEPATOTOXICITY; PHARMACOKINETICS; LOPINAVIR/RITONAVIR; NEVIRAPINE; IMPAIRMENT; NELFINAVIR;
D O I
10.1093/jac/dkq320
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To compare plasma antiretroviral concentrations in HIV-HCV co-infected and in matched HIV mono-infected patients. 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. 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. 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.
引用
收藏
页码:2445 / 2449
页数:5
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