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Neurology. 2014 Jul 8;83(2):134-41. doi: 10.1212/WNL.0000000000000564. Epub 2014 Jun 6.
The link between CNS penetration of antiretrovirals and AIDS-defining neurologic disorders remains largely unknown.
HIV-infected, antiretroviral therapy-naive individuals in the HIV-CAUSAL Collaboration who started an antiretroviral regimen were classified according to the CNS Penetration Effectiveness (CPE) score of their initial regimen into low (<8), medium (8-9), or high (>9) CPE score. We estimated "intention-to-treat" hazard ratios of 4 neuroAIDS conditions for baseline regimens with high and medium CPE scores compared with regimens with a low score. We used inverse probability weighting to adjust for potential bias due to infrequent follow-up.
A total of 61,938 individuals were followed for a median (interquartile range) of 37 (18, 70) months. During follow-up, there were 235 cases of HIV dementia, 169 cases of toxoplasmosis, 128 cases of cryptococcal meningitis, and 141 cases of progressive multifocal leukoencephalopathy. The hazard ratio (95% confidence interval) for initiating a combined antiretroviral therapy regimen with a high vs low CPE score was 1.74 (1.15, 2.65) for HIV dementia, 0.90 (0.50, 1.62) for toxoplasmosis, 1.13 (0.61, 2.11) for cryptococcal meningitis, and 1.32 (0.71, 2.47) for progressive multifocal leukoencephalopathy. The respective hazard ratios (95% confidence intervals) for a medium vs low CPE score were 1.01 (0.73, 1.39), 0.80 (0.56, 1.15), 1.08 (0.73, 1.62), and 1.08 (0.73, 1.58).
We estimated that initiation of a combined antiretroviral therapy regimen with a high CPE score increases the risk of HIV dementia, but not of other neuroAIDS conditions.
抗逆转录病毒药物对中枢神经系统的穿透性与艾滋病相关神经障碍之间的联系在很大程度上仍不清楚。
HIV-CAUSAL 合作组织中感染 HIV、未接受过抗逆转录病毒治疗的个体,根据初始治疗方案的中枢神经系统穿透效果(CPE)评分,分为低(<8)、中(8-9)或高(>9)CPE 评分组。我们估计了高和中 CPE 评分的基线方案与低评分方案相比,4 种神经艾滋病状况的“意向治疗”风险比。我们使用逆概率加权法来调整因随访不频繁而导致的潜在偏倚。
共有 61938 人接受了中位数(四分位间距)为 37(18,70)个月的随访。在随访期间,有 235 例 HIV 痴呆,169 例弓形体病,128 例隐球菌性脑膜炎和 141 例进行性多灶性白质脑病。高 CPE 评分与低 CPE 评分相比,起始联合抗逆转录病毒治疗方案的风险比(95%置信区间)为 HIV 痴呆 1.74(1.15,2.65),弓形体病 0.90(0.50,1.62),隐球菌性脑膜炎 1.13(0.61,2.11),进行性多灶性白质脑病 1.32(0.71,2.47)。中 CPE 评分与低 CPE 评分相比的相应风险比(95%置信区间)分别为 1.01(0.73,1.39)、0.80(0.56,1.15)、1.08(0.73,1.62)和 1.08(0.73,1.58)。
我们估计,起始高 CPE 评分的联合抗逆转录病毒治疗方案会增加 HIV 痴呆的风险,但不会增加其他神经艾滋病状况的风险。