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增强针对人类免疫缺陷病毒认知障碍的抗逆转录病毒疗法。

Enhancing antiretroviral therapy for human immunodeficiency virus cognitive disorders.

作者信息

Letendre Scott L, McCutchan J Allen, Childers Meredith E, Woods Steven P, Lazzaretto Deborah, Heaton Robert K, Grant Igor, Ellis Ronald J

机构信息

HIV Neurobehavioral Research Center, University of California at San Diego, San Diego, CA 92103, USA.

出版信息

Ann Neurol. 2004 Sep;56(3):416-23. doi: 10.1002/ana.20198.

Abstract

The benefits of combination antiretroviral therapy (ART) for HIV cognitive disorders vary substantially between individuals. This study evaluated whether cerebrospinal fluid (CSF) drug penetration and CSF virological suppression influence the extent of neuropsychological (NP) improvement during ART. Overall performance on a battery of NP tests administered at baseline and follow-up (median 15 weeks) was computed by using the global deficit score (GDS) methods in 31 cognitively impaired, HIV-infected individuals who began new ART regimens. Virological suppression (attaining undetectable viral load by RT-PCR at follow-up) was assessed separately for plasma and CSF. Subjects on regimens containing greater numbers of CSF-penetrating drugs showed significantly greater reduction in CSF viral load. Subjects attaining CSF virological suppression demonstrated greater GDS improvement than those who did not (median GDS change, 0.62 vs 0.23; p = 0.01). A similar trend for plasma did not reach statistical significance (p = 0.053). NP improvement was greater in ART-naive versus treatment-experienced subjects. In a multivariate model (overall p = 0.0008), significant, independent predictors of GDS reduction were CSF HIV RNA suppression, baseline antiretroviral history, and their interaction. Including CSF-penetrating drugs in the ART regimen and monitoring CSF viral load may be indicated for individuals with HIV-associated cognitive impairment.

摘要

联合抗逆转录病毒疗法(ART)对HIV认知障碍的益处因个体差异很大。本研究评估了脑脊液(CSF)药物渗透和脑脊液病毒学抑制是否会影响ART期间神经心理学(NP)改善的程度。在31名开始新ART方案的认知受损HIV感染者中,采用整体缺陷评分(GDS)方法计算了在基线和随访(中位数15周)时进行的一系列NP测试的总体表现。分别评估了血浆和脑脊液的病毒学抑制情况(随访时通过逆转录聚合酶链反应检测不到病毒载量)。接受含有更多脑脊液穿透性药物方案的受试者脑脊液病毒载量下降更为显著。实现脑脊液病毒学抑制的受试者比未实现的受试者GDS改善更大(GDS变化中位数,0.62对0.23;p = 0.01)。血浆方面的类似趋势未达到统计学显著性(p = 0.053)。初治受试者比有治疗经验的受试者NP改善更大。在多变量模型中(总体p = 0.0008),GDS降低的显著独立预测因素是脑脊液HIV RNA抑制、基线抗逆转录病毒治疗史及其相互作用。对于患有HIV相关认知障碍的个体,ART方案中纳入脑脊液穿透性药物并监测脑脊液病毒载量可能是必要的。

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