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The lopinavir/ritonavir-associated rise in lipids is not related to lopinavir or ritonavir plasma concentration.

机译:洛匹那韦/利托那韦相关脂质的升高与洛匹那韦或利托那韦血浆浓度无关。

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BACKGROUND: The relationship between lopinavir plasma concentration and the magnitude of lipid elevation after initiation of lopinavir/ritonavir-containing antiretroviral therapy is unclear. The aim of this study was to determine the relationship between drug concentration and lipid changes in two patient cohorts. METHODS: First, we analysed, in an outpatient cohort, the correlation between percentage lipid changes and lopinavir concentration, measured at least 2 weeks or more after initiation of lopinavir/ritonavir. Second, we analysed the correlation between lipid changes and lopinavir and ritonavir plasma concentrations in antiretroviral-naive patients enrolled in a trial comparing nevirapine plus lopinavir/ritonavir (533/133 mg twice daily) with zidovudine/lamivudine plus lopinavir/ritonavir (400/100 mg twice daily). RESULTS: In 82 outpatients with 215 lopinavir plasma measurements, we found no significant correlations between lopinavir concentration and changes in lipids a median of 522 days after lopinavir/ritonavir initiation in univariable regression analyses, nor in multivariable analyses adjusting for potential confounders. In 40 trial samples collected 24 months after treatment initiation, the mean (95% CI) percentage increase in low-density lipoprotein cholesterol (LDLc) was significantly greater in the nevirapine/lopinavir/ritonavir group (29.4% [16.8-43.3]) than in the zidovudine/lamivudine/lopinavir/ritonavir group (6.8% [-7.3-23.1]; P=0.03). However, the percentage LDLc change did not correlate with lopinavir or ritonavir concentration ratios (r=-0.25; P=0.17 and r=-0.06; P=0.75). Adding lopinavir or ritonavir concentrations into the multivariable regression analyses did not change the relation between LDLc change and randomized treatment. CONCLUSIONS: Neither in an HIV outpatient clinic cohort nor in a trial comparing two lopinavir/ritonavir-containing therapies did we find any relation between changes in lipids, and lopinavir and ritonavir concentration, after initiating lopinavir/ritonavir-containing treatment.
机译:背景:洛匹那韦/含利托那韦的抗逆转录病毒疗法启动后,洛匹那韦血浆浓度与脂质升高幅度之间的关系尚不清楚。这项研究的目的是确定两个患者队列中药物浓度和脂质变化之间的关系。方法:首先,我们在门诊队列中分析了在开始使用洛匹那韦/利托那韦至少2周或更长时间后测得的脂质变化百分比与洛匹那韦浓度之间的相关性。其次,我们在一项试验中比较了初次接受抗逆转录病毒治疗的初次接受抗逆转录病毒治疗的患者的脂质变化与洛匹那韦和利托那韦血浆浓度之间的相关性,该研究比较了奈韦拉平加洛匹那韦/利托那韦(每天533/133 mg)与齐多夫定/拉米夫定加洛匹那韦/利托那韦(400/100)每天两次)。结果:在82例洛匹那韦血浆测定的门诊患者中,在单变量回归分析中或在校正潜在混杂因素的多变量分析中,洛匹那韦/利托那韦起始后522天的中位数为522天,洛匹那韦浓度与脂质变化之间无显着相关性。在开始治疗后24个月收集的40个试验样品中,奈韦拉平/洛匹那韦/利托那韦组的低密度脂蛋白胆固醇(LDLc)平均增加(95%CI)百分比(29.4%[16.8-43.3])比齐多夫定/拉米夫定/洛匹那韦/利托那韦组(6.8%[-7.3-23.1]; P = 0.03)。但是,LDLc的变化百分比与洛匹那韦或利托那韦浓度比不相关(r = -0.25; P = 0.17; r = -0.06; P = 0.75)。在多变量回归分析中添加洛匹那韦或利托那韦浓度未改变LDLc改变与随机治疗之间的关系。结论:既没有在艾滋病门诊诊所队列中,也没有在比较两种含洛匹那韦/利托那韦的疗法的试验中,在开始使用含洛匹那韦/利托那韦的治疗后,我们没有发现脂质变化,洛匹那韦和利托那韦浓度之间有任何关系。

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