Baker Jason V, Sharma Shweta, Achhra Amit C, Bernardino Jose Ignacio, Bogner Johannes R, Duprez Daniel, Emery Sean, Gazzard Brian, Gordin Jonathan, Grandits Greg, Phillips Andrew N, Schwarze Siegfried, Soliman Elsayed Z, Spector Stephen A, Tambussi Giuseppe, Lundgren Jens
Department of Medicine, University of Minnesota, Minneapolis, MN
Division of Infectious Diseases, Hennepin County Medical Center, Minneapolis, MN.
J Am Heart Assoc. 2017 May 22;6(5):e004987. doi: 10.1161/JAHA.116.004987.
HIV infection and certain antiretroviral therapy (ART) medications increase atherosclerotic cardiovascular disease risk, mediated, in part, through traditional cardiovascular disease risk factors.
We studied cardiovascular disease risk factor changes in the START (Strategic Timing of Antiretroviral Treatment) trial, a randomized study of immediate versus deferred ART initiation among HIV-positive persons with CD4 cell counts >500 cells/mm. Mean change from baseline in risk factors and the incidence of comorbid conditions were compared between groups. The characteristics among 4685 HIV-positive START trial participants include a median age of 36 years, a CD4 cell count of 651 cells/mm, an HIV viral load of 12 759 copies/mL, a current smoking status of 32%, a median systolic/diastolic blood pressure of 120/76 mm Hg, and median levels of total cholesterol of 168 mg/dL, low-density lipoprotein cholesterol of 102 mg/dL, and high-density lipoprotein cholesterol of 41 mg/dL. Mean follow-up was 3.0 years. The immediate and deferred ART groups spent 94% and 28% of follow-up time taking ART, respectively. Compared with patients in the deferral group, patients in the immediate ART group had increased total cholesterol and low-density lipoprotein cholesterol and higher use of lipid-lowering therapy (1.2%; 95% CI, 0.1-2.2). Concurrent increases in high-density lipoprotein cholesterol with immediate ART resulted in a 0.1 lower total cholesterol to high-density lipoprotein cholesterol ratio (95% CI, 0.1-0.2). Immediate ART resulted in 2.3% less BP-lowering therapy use (95% CI, 0.9-3.6), but there were no differences in new-onset hypertension or diabetes mellitus.
Among HIV-positive persons with preserved immunity, immediate ART led to increases in total cholesterol and low-density lipoprotein cholesterol but also concurrent increases in high-density lipoprotein cholesterol and decreased use of blood pressure medications. These opposing effects suggest that, in the short term, the net effect of early ART on traditional cardiovascular disease risk factors may be clinically insignificant."
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00867048.
HIV感染和某些抗逆转录病毒疗法(ART)药物会增加动脉粥样硬化性心血管疾病的风险,部分是通过传统的心血管疾病风险因素介导的。
我们在START(抗逆转录病毒治疗的战略时机)试验中研究了心血管疾病风险因素的变化,这是一项针对CD4细胞计数>500个细胞/mm的HIV阳性者进行即刻与延迟开始ART治疗的随机研究。比较了两组之间风险因素从基线的平均变化以及合并症的发生率。4685名HIV阳性START试验参与者的特征包括:年龄中位数为36岁,CD4细胞计数为651个细胞/mm,HIV病毒载量为12759拷贝/mL,当前吸烟率为32%,收缩压/舒张压中位数为120/76 mmHg,总胆固醇中位数水平为168 mg/dL,低密度脂蛋白胆固醇为102 mg/dL,高密度脂蛋白胆固醇为41 mg/dL。平均随访时间为3.0年。即刻ART组和延迟ART组分别有94%和28%的随访时间接受ART治疗。与延迟组患者相比,即刻ART组患者的总胆固醇和低密度脂蛋白胆固醇升高,降脂治疗的使用率更高(1.2%;95%CI,0.1 - 2.2)。即刻ART治疗同时使高密度脂蛋白胆固醇升高,导致总胆固醇与高密度脂蛋白胆固醇之比降低0.1(95%CI,0.1 - 0.2)。即刻ART治疗使降压治疗的使用率降低2.3%(95%CI,0.9 - 3.6),但新发高血压或糖尿病无差异。
在免疫功能保留的HIV阳性者中,即刻ART治疗导致总胆固醇和低密度脂蛋白胆固醇升高,但同时高密度脂蛋白胆固醇也升高,且降压药物的使用减少。这些相反的作用表明,短期内,早期ART治疗对传统心血管疾病风险因素的净效应在临床上可能不显著。