首页> 外文期刊>AIDS Research and Human Retroviruses >Inflammatory biomarker changes and their correlation with framingham cardiovascular risk and lipid changes in antiretroviral-naive HIV-infected patients treated for 144 weeks with abacavir/lamivudine/atazanavir with or without ritonavir in ARIES
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Inflammatory biomarker changes and their correlation with framingham cardiovascular risk and lipid changes in antiretroviral-naive HIV-infected patients treated for 144 weeks with abacavir/lamivudine/atazanavir with or without ritonavir in ARIES

机译:在ARIES中接受或不接受ritonavir的阿巴卡韦/拉米夫定/阿扎那韦治疗144周的抗逆转录病毒初治HIV感染患者中,炎症生物标志物变化及其与弗雷明汉心血管风险和脂质变化的相关性

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Propensity for developing coronary heart disease (CHD) is linked with Framingham-defined cardiovascular risk factors and elevated inflammatory biomarkers. Cardiovascular risk and inflammatory biomarkers were evaluated in ARIES, a Phase IIIb/IV clinical trial in which 515 antiretroviral-naive HIV-infected subjects initially received abacavir/lamivudine + atazanavir/ritonavir for 36 weeks. Subjects who were virologically suppressed by week 30 were randomized 1:1 at week 36 to either maintain or discontinue ritonavir for an additional 108 weeks. Framingham 10-year CHD risk scores (FRS) and risk category of 6% or ≥6%, lipoprotein-associated phospholipase A2 (Lp-PLA2), interleukin-6 (IL-6), and high-sensitivity C-reactive protein (hsCRP) were assessed at baseline, week 84, and week 144. Biomarkers were stratified by FRS category. When ritonavir-boostedonboosted treatment groups were combined, median hsCRP did not change significantly between baseline (1.6 mg/liter) and week 144 (1.4 mg/liter) in subjects with FRS 6% (p=0.535) or with FRS ≥6% (1.9 mg/liter vs. 2.0 mg/liter, respectively; p=0.102). Median IL-6 was similar for subjects with FRS 6% (p=0.267) at baseline (1.6 pg/ml) and week 144 (1.4 pg/ml) and for FRS ≥6% (2.0 pg/ml vs. 2.2 pg/ml, respectively; p=0.099). Median Lp-PLA2 decreased significantly (p0.001) between baseline (197 nmol/min/ml) and week 144 (168 nmol/min/ml) in subjects with FRS 6% and with FRS ≥6% (238 nmol/min/ml vs. 175 nmol/min/ml, respectively; p0.001). In conclusion, in antiretroviral-naive subjects treated with abacavir-based therapy for 144 weeks, median inflammatory biomarker levels for hsCRP and IL-6 generally remained stable with no significant difference between baseline and week 144 for subjects with either FRS 6% or FRS ≥6%. Lp-PLA2 median values declined significantly over 144 weeks for subjects in either FRS stratum.
机译:患冠心病(CHD)的倾向与Framingham定义的心血管危险因素和炎性生物标志物升高有关。在ARIES(IIIb / IV期临床试验)中评估了心血管风险和炎性生物标志物,其中515名抗逆转录病毒初次感染HIV的受试者最初接受阿巴卡韦/拉米夫定+阿扎那韦/利托那韦治疗36周。在第30周被病毒学抑制的受试者在第36周按1:1的比例随机分配,以维持或停用利托那韦另外108周。弗雷明汉10年冠心病危险评分(FRS),危险类别<6%或≥6%,脂蛋白相关磷脂酶A2(Lp-PLA2),白细胞介素6(IL-6)和高敏感性C反应蛋白(hsCRP)在基线,第84周和第144周进行评估。按FRS类别对生物标志物进行分层。当FRS <6%(p = 0.535)或FRS≥的受试者合并利托那韦增强/非增强治疗组时,hsCRP中位数在基线(1.6 mg /升)和144周(1.4 mg /升)之间没有显着变化。 6%(分别为1.9 mg / l和2.0 mg / l; p = 0.102)。在基线(1.6 pg / ml)和144周(1.4 pg / ml)时FRS <6%(p = 0.267)的受试者和FRS≥6%(2.0 pg / ml vs. 2.2 pg)的受试者中位数IL-6相似/ml;p=0.099)。 FRS <6%和FRS≥6%(238 nmol / min)的受试者在基线(197 nmol / min / ml)和第144周(168 nmol / min / ml)之间的中值Lp-PLA2显着降低(p <0.001) / ml分别为175 nmol / min / ml; p <0.001)。总之,在未经抗逆转录病毒治疗的受试者中,以abacavir为基础的治疗144周,hsCRP和IL-6的炎症生物标志物水平中值通常保持稳定,对于FRS <6%或FRS的受试者,基线和144周之间无显着差异≥6%。在任一FRS阶层中,受试者的Lp-PLA2中值在144周内均显着下降。

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