Effect of accompanying antiretroviral drugs on virological response to pegylated interferon and ribavirin in patients co-infected with HIV and hepatitis C virus

被引:13
作者
Berenguer, Juan [1 ]
von Wichmann, Miguel A. [2 ]
Quereda, Carmen [3 ]
Miralles, Pilar
Mallolas, Josep [4 ]
Lopez-Aldeguer, Jose [5 ]
Alvarez-Pellicer, Julio
De Miguel, Julio [6 ]
Crespo, Manel [7 ]
Guardiola, Josep M. [8 ]
Tellez, Maria J. [9 ]
Galindo, Maria J. [10 ]
Arponen, Sari
Barquilla, Elena [11 ]
Bellon, Jose M.
Gonzalez-Garcia, Juan
机构
[1] Hosp Gen Univ Gregorio Maranon, Unidad Enfermedades Infecciosas VIH 4100, Madrid 28007, Spain
[2] Hosp Donostia, San Sebastian, Spain
[3] Hosp Ramon & Cajal, E-28034 Madrid, Spain
[4] Hosp Clin Barcelona, Barcelona, Spain
[5] Hosp La Fe, E-46009 Valencia, Spain
[6] Hosp Principe de Asturias, Alcala De Henares, Spain
[7] Hosp Valle De Hebron, Barcelona, Spain
[8] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[9] Hosp Clin San Carlos, Madrid, Spain
[10] Hosp Clin Univ, Valencia, Spain
[11] Fdn SEIMC GESIDA, Madrid, Spain
关键词
HIV infection; HCV; ribavirin antiviral agents; drug interactions; HUMAN-IMMUNODEFICIENCY-VIRUS; ALPHA-2B PLUS RIBAVIRIN; MITOCHONDRIAL TOXICITY; COINFECTED PATIENTS; INSULIN-RESISTANCE; HIV/HCV-COINFECTION; TREATMENT DURATION; GENETIC-VARIATION; RISK-FACTORS; PEGINTERFERON;
D O I
10.1093/jac/dkr362
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The effects of antiretroviral drugs on the response to pegylated interferon plus ribavirin remain uncertain. We evaluated whether antiretroviral drugs affected the response to pegylated interferon plus ribavirin in patients co-infected with HIV and hepatitis C virus (HCV). Methods: We conducted a retrospective analysis of two cohorts of HIV/HCV-co-infected patients treated with pegylated interferon plus ribavirin between 2001 and 2007 in Spain. The outcome measure was sustained virological response (SVR). Logistic regression models were used to test possible associations between non-response and pre-treatment characteristics, including accompanying antiretroviral drugs. Results: The study sample comprised 1701 patients: 63% were infected with HCV genotype (G) 1 or 4 and 88% were taking highly active antiretroviral therapy (HAART). Factors independently associated with increased odds of SVR were G2 or 3, HVC RNA,500000 IU/mL and CDC clinical category A or B. When we adjusted for these prognostic factors and dose of ribavirin/kg, the adjusted odds ratio (AOR) of SVR for patients without HAART was 1.31 [95% confidence interval (CI) 0.91-1.88; P=0.144]. Taking the backbone of tenofovir and lamivudine/emtricitabine as a reference, we found that, with the exception of regimens including zidovudine, the effect of other nucleoside reverse transcriptase inhibitor backbones had little effect on SVR. The AOR of SVR for zidovudine and lamivudine was 0.65 (95% CI 0.46-0.93, P=0.017). We carried out several sensitivity analyses, the results of which were consistent with the findings of the primary analysis. Conclusions: Our results suggest that, with the exception of regimens including zidovudine, accompanying antiretroviral drugs have little effect on the virological response to pegylated interferon plus ribavirin in HIV/HCV-co-infected patients.
引用
收藏
页码:2843 / 2849
页数:7
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