阿扎那韦/利托那韦与达那韦/利托那韦治疗naïve hiv -1感染患者的炎症作用

Q2 Medicine HIV Clinical Trials Pub Date : 2018-08-01 Epub Date: 2018-11-13 DOI:10.1080/15284336.2018.1488453
Chiara Dentone, Antonio Di Biagio, Alessandro Cozzi Lepri, Daniela Fenoglio, Gilberto Filaci, Miriam Lichtner, Stefania Carrara, Andrea Giacometti, Laura Sighinolfi, Giulia Marchetti, Andrea Antinori, Antonella D'arminio Monforte
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引用次数: 3

摘要

背景:有限的研究比较了不同抗逆转录病毒治疗方案对可溶性炎症标志物的影响,结果不一致。方法:在这项前瞻性研究中,治疗naïve hiv -1感染的患者,如果他们开始目前的方案阿扎那韦/利托那韦(ATV/r) (N = 73,组1)或达那韦/利托那韦(DRV/r) (N = 85,组2)加替诺福韦/恩曲他滨。对两份储存的血浆样本进行IL-6、MCP-1、sCD163、VCAM-1、ox-LDL和脂联素分析,第一份是在抗逆转录病毒治疗开始前,第二份是在开始治疗一年后。结果:通过匹配设计或线性回归模型控制ox-LDL基线水平及其他潜在的混杂因素后,我们的分析结果显示,基于ATV/r的两组之间ox-LDL的差异(SD值较高)为608.5±137.4,而DRV/r组为519.1±119.6。结论:我们的分析提供了进一步的数据,研究了在暴露于这些药物一年以上的特定蛋白酶抑制剂治疗中血管炎症调节和激活标记物之间的关系。数据显示很少有证据表明两者之间存在关联,这支持了抗逆转录病毒治疗方案在下调这些可溶性标记物方面通常效率较低的观点。
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Inflammatory effects of atazanavir/ritonavir versus darunavir/ritonavir in treatment naïve, HIV-1-infected patients.

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 naïve 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.

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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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