Foundation Lluita against AIDS, University Hospital Germans Trias i Pujol, Badalona, Spain.
Statistics and Operations Research, Technical University of Catalonia, Barcelona, 08020, Spain.
HIV Med. 2017 Nov;18(10):782-786. doi: 10.1111/hiv.12530. Epub 2017 Jul 3.
Cobicistat seems to have a low rate of adverse events compared with ritonavir.
This restrospective observational study to evaluated changes in lipid parameters and the percentage of subjects with dyslipidemia in virologically suppressed HIV-infected patients who were receiving a regimen containing darunavir/ritonavir and were then switched from ritonavir to cobicistat, carried out from December 2015 to May 2016, included 299 HIV-1-infected patients who were on stable antiretroviral treatment including darunavir/ritonavir (monotherapy, bitherapy or triple therapy for at least 6 months) and were then switched from ritonavir to cobicistat. Lipid parameters, as well as plasma HIV-1 RNA and CD4 cell counts, were recorded at baseline just before the switch, and 24 weeks after the switch. Patients were stratified according to the presence of hypercholesterolaemia [baseline total cholesterol > 200 mg/dL and/or low-density lipoprotein (LDL) cholesterol > 130 mg/dL] or hypertriglyceridaemia (baseline triglyceride levels > 200 mg/dL).
Two hundred and ninety-nine patients were enrolled in the study. Fifty-two per cent of the total study population showed dyslipidaemia at baseline. All patients maintained HIV-1 RNA ≤ 50 HIV-1 RNA copies/mL at week 24. No statistically significant changes were seen in CD4 T-cell count from baseline to week 24 [654 (298) to 643 (313) cells/μL; P = 0.173]. When patients were stratified according to the presence of hypercholesterolaemia at baseline (n = 124), significant changes were observed in total cholesterol (P < 0.001), LDL cholesterol (P = 0.047), high-density lipoprotein (HDL) cholesterol (P = 0.002) and triglyceride levels (P = 0.025), and when they were stratified according to the presence of hypertriglyceridaemia at baseline (n = 64), changes from baseline to week 24 in triglyceride level were statistically significant [median (interquartile range) 352 (223, 389) mg/dL at baseline and 229 (131, 279) mg/dL at week 24; P < 0.001].
Cobicistat as a booster of darunavir in HIV-infected subjects had a beneficial effect on the lipid profile in patients with hypercholesterolaemia or hypertrigliceridaemia at baseline.
与利托那韦相比,考比司他的不良反应发生率似乎较低。
本回顾性观察研究评估了在接受达芦那韦/利托那韦治疗且病毒学抑制的 HIV 感染患者中,从利托那韦转换为考比司他后,血脂参数的变化和血脂异常患者的比例。该研究于 2015 年 12 月至 2016 年 5 月进行,共纳入 299 例接受稳定抗逆转录病毒治疗(至少 6 个月的达芦那韦/利托那韦单药、双药或三药治疗)且从利托那韦转换为考比司他的 HIV-1 感染患者。在转换前的基线和转换后 24 周记录血脂参数、血浆 HIV-1 RNA 和 CD4 细胞计数。根据基线时总胆固醇>200mg/dL 和/或低密度脂蛋白(LDL)胆固醇>130mg/dL(高胆固醇血症)或基线时甘油三酯水平>200mg/dL(高甘油三酯血症)存在情况对患者进行分层。
共纳入 299 例患者。总研究人群中有 52%在基线时存在血脂异常。所有患者在第 24 周时 HIV-1 RNA 均≤50 HIV-1 RNA 拷贝/mL。从基线到第 24 周,CD4 T 细胞计数无统计学显著变化[654(298)至 643(313)细胞/μL;P=0.173]。根据基线时高胆固醇血症的存在情况(n=124)对患者进行分层时,总胆固醇(P<0.001)、LDL 胆固醇(P=0.047)、高密度脂蛋白(HDL)胆固醇(P=0.002)和甘油三酯水平有显著变化,根据基线时高甘油三酯血症的存在情况(n=64)对患者进行分层时,从基线到第 24 周时甘油三酯水平的变化有统计学意义[中位数(四分位距)基线时 352(223,389)mg/dL 和第 24 周时 229(131,279)mg/dL;P<0.001]。
考比司他作为 HIV 感染患者达芦那韦的增效剂,对基线时存在高胆固醇血症或高甘油三酯血症的患者的血脂谱有有益影响。