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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
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.
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页码:2445 / 2449
页数:5
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