Empilweni Services and Research Unit, Rahima Moosa Mother and Child Hospital, University of the Witwatersrand, Johannesburg, South Africa.
J Acquir Immune Defic Syndr. 2012 Aug 1;60(4):369-76. doi: 10.1097/QAI.0b013e318243760b.
Both HIV infection and antiretroviral therapy are associated with dyslipidemias in adults, but there are fewer data on outcomes in young children. Here we examined lipid profile changes in a cohort of young children before and after suppression on an initial ritonavir-boosted lopinavir (LPV/r)-based regimen and after switch to a nevirapine (NVP)-based regimen.
One hundred ninety-five HIV-infected children who initiated LPV/r-based therapy when <24 months of age at 1 site in Johannesburg, South Africa, and who achieved viral suppression (<400 copies/mL sustained for ≥ 3 months) were randomized to either continue on the LPV/r-based regimen (n = 99) or to switch to a NVP-based regimen (n = 96). Nonfasting concentrations of total cholesterol (TC), low-density lipoprotein, high-density lipoprotein (HDL), and triglycerides (TG) were measured pretreatment, at randomization when suppressed, and at 9, 20, and 31 months postrandomization.
Median age at treatment initiation was 9 months, and the initial regimen was maintained for an average of 9 months before randomization. TC, low-density lipoprotein, and HDL increased from pretreatment to randomization (P < 0.0001) and TC/HDL ratio and TG decreased (P < 0.0001). After switching to NVP, HDL was significantly higher (P < 0.02) and TC/HDL and TG significantly lower (P < 0.0001) through 31 months postswitch relative to remaining on the LPV/r-based regimen.
Initiating antiretroviral therapy was associated with changes to a more favorable lipid profile in young children. Switching from a LPV/r-based regimen to a NVP-based regimen accentuated and continued these improvements. Investigation of safe and effective methods for managing dyslipidemias in children of different ages in resource-limited settings is warranted.
HIV 感染和抗逆转录病毒治疗都会导致成年人血脂异常,但针对幼儿的相关数据较少。在此,我们研究了在约翰内斯堡的一个研究点,一组接受利托那韦增强洛匹那韦(LPV/r)为基础的方案初始治疗、病毒得到抑制(持续 3 个月以上<400 拷贝/mL)的幼儿,在转换为奈韦拉平(NVP)为基础的方案前后的血脂谱变化。
在南非约翰内斯堡的一个研究点,195 名年龄<24 个月的 HIV 感染儿童开始 LPV/r 为基础的治疗,且病毒得到抑制,他们被随机分配继续接受 LPV/r 为基础的方案(n=99)或转换为 NVP 为基础的方案(n=96)。在治疗前、随机时抑制病毒、9、20 和 31 个月后测量非空腹总胆固醇(TC)、低密度脂蛋白、高密度脂蛋白(HDL)和甘油三酯(TG)的浓度。
治疗开始时的中位年龄为 9 个月,初始方案平均维持 9 个月后开始随机分配。TC、低密度脂蛋白和 HDL 从治疗前到随机时升高(P<0.0001),TC/HDL 比值和 TG 降低(P<0.0001)。转换为 NVP 后,与继续接受 LPV/r 为基础的方案相比,HDL 在 31 个月后一直显著升高(P<0.02),TC/HDL 和 TG 显著降低(P<0.0001)。
开始抗逆转录病毒治疗与幼儿更有利的血脂谱变化有关。从 LPV/r 为基础的方案转换为 NVP 为基础的方案,强化并持续了这些改善。需要在资源有限的环境中,对不同年龄的儿童管理血脂异常的安全有效的方法进行调查。