Inflammatory effects of atazanavir/ritonavir versus darunavir/ritonavir in treatment naive, HIV-1-infected patients

被引:1
作者
Dentone, Chiara [1 ]
Di Biagio, Antonio [2 ]
Lepri, Alessandro Cozzi [3 ]
Fenoglio, Daniela [4 ,5 ]
Filaci, Gilberto [4 ,5 ]
Lichtner, Miriam [6 ]
Carrara, Stefania [7 ]
Giacometti, Andrea [8 ]
Sighinolfi, Laura [9 ]
Marchetti, Giulia [10 ]
Antinori, Andrea [7 ]
Monforte, Antonella D'arminio [10 ]
Monforte, A. d'Arminio
Antinori, A.
Castagna, A.
Castelli, F.
Cauda, R.
Di Perri, G.
Galli, M.
Iardino, R.
Ippolito, G.
Lazzarin, A.
Marchetti, G. C.
Perno, C. F.
Rezza, G.
von Schloesser, F.
Viale, P.
Monforte, A. d'Arminio
Antinori, A.
Castagna, A.
Ceccherini-Silberstein, F.
Cozzi-Lepri, A.
Girardi, E.
Lo Caputo, S.
Mussini, C.
Puoti, M.
机构
[1] Sanremo Hosp, Infect Dis Unit, Imperia, Italy
[2] Osped Policlin S Martino, Dept Internal Med, Infect Dis Unit, Genoa, Italy
[3] Inst Global Hlth UCL, Ctr Clin Res Epidemiol Modelling & Evaluat CREME, Rowland Hill St, London, England
[4] Univ Genoa, Ctr Excellence Biomed Res, Genoa, Italy
[5] Univ Genoa, Osped Policlin San Martino, Dept Internal Med DIMI, Genoa, Italy
[6] Sapienza Univ, Infect Dis Unit, Latina, Italy
[7] IRCCS, Natl Inst Infect Dis INMI L Spallanzani, Rome, Italy
[8] Azienda OU Osped Riuniti Ancona, Clin Infect Dis, Ancona, Italy
[9] Hosp & Univ Ferrara, Clin Malattie Infett, Ferrara, Italy
[10] Univ Milan, San Paolo Hosp, Clin Malattie Infett, Milan, Italy
来源
HIV CLINICAL TRIALS | 2018年 / 19卷 / 04期
关键词
Vascular inflammation; activation markers; first-line antiretroviral therapy; atazanavir; darunavir; HIV; HIV-INFECTION; ANTIRETROVIRAL THERAPY; IMMUNE ACTIVATION; TENOFOVIR/EMTRICITABINE; MECHANISMS; EFAVIRENZ;
D O I
10.1080/15284336.2018.1488453
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Limited studies have compared the impact of different antiretroviral regimens on soluble markers of inflammation with discordant results. Methods: In this prospective study, treatment naive HIV-1-infected patients were included if they started their current regimen with atazanavir/ritonavir (ATV/r) (N = 73, Group 1) or darunavir/ritonavir (DRV/r) (N = 85, Group 2) plus tenofovir/emtricitabine. The analysis of IL-6, MCP-1, sCD163, VCAM-1, ox-LDL, and adiponectine was performed on two stored plasma samples, the first prior to antiretroviral therapy initiation and the second one year after initiation. Results: The results of our analysis show a difference in ox-LDL between the two groups with higher mean (SD) values in ATV/r based group 608.5 +/- 137.4 versus 519.1 +/- 119.6 in DRV/r group, after controlling for baseline levels of ox-LDL as well as other potential confounding factors controlled by means of matching design or linear regression modelling. Conclusions: Our analysis provides further data examining the association between the modulation of vascular inflammatory and of activation markers with specific protease inhibitors-based treatments over one year of exposure to these drugs. The data show little evidence for an association, supporting the notion that antiretroviral regimens has generally poor efficiency in downregulating these soluble markers.
引用
收藏
页码:158 / 162
页数:5
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