Department of Neurology, Yale University School of Medicine, New Haven, Connecticut.
Center for Neuroepidemiology and Clinical Neurological Research, Yale University School of Medicine, New Haven, Connecticut.
Semin Neurol. 2019 Jun;39(3):391-398. doi: 10.1055/s-0039-1688915. Epub 2019 Aug 2.
Treatment of neurological, neurocognitive, and neuropsychiatric impairment in the setting of human immunodeficiency virus (HIV) infection remains a complex problem, given several possible mechanisms of pathogenesis. The etiology must be determined based on clinical judgment and objective evidence, including cerebrospinal fluid (CSF) data from lumbar puncture and neuroimaging information from magnetic resonance imaging, when available and indicated. Other neuroinfectious etiologies must be ruled out, including central nervous system (CNS) opportunistic infections. HIV replication in the CNS (including CSF escape) should be evaluated for and excluded. If CSF HIV is detected, we recommend a treatment switch to antiretrovirals (ARVs) targeted to address any CSF HIV resistance mutations identified, or empiric treatment intensification using ARVs with high CNS penetration. If CSF HIV is not detected, treatment intensification with CCR5 inhibitors may be considered as an adjunct to reduce neuroinflammation. Finally, the current ARV regimen must be examined for possible neurotoxicity. Efavirenz has been well-recognized for its neuropsychiatric adverse effects and potential for causing sleep disturbances. Similar concerns have recently been raised with integrase inhibitors, especially dolutegravir and raltegravir, although further studies are needed to determine the risks for clinically relevant neuropsychiatric side effects from these medications, given their overall high potency and proven success in treating systemic HIV.
治疗人类免疫缺陷病毒(HIV)感染相关的神经、神经认知和神经精神障碍仍然是一个复杂的问题,因为存在多种可能的发病机制。病因必须基于临床判断和客观证据来确定,包括腰椎穿刺的脑脊液(CSF)数据和磁共振成像的神经影像学信息,在有条件和指征时使用。还必须排除其他神经感染性病因,包括中枢神经系统(CNS)机会性感染。应评估并排除 HIV 在中枢神经系统(包括 CSF 逃逸)中的复制。如果 CSF 中检测到 HIV,我们建议根据发现的任何 CSF HIV 耐药突变,将抗逆转录病毒药物(ARV)转换为靶向治疗,或者使用具有高中枢神经系统穿透性的 ARV 进行经验性治疗强化。如果 CSF 中未检测到 HIV,可以考虑使用 CCR5 抑制剂强化治疗作为辅助手段,以减轻神经炎症。最后,必须检查当前的 ARV 方案是否存在潜在的神经毒性。依非韦伦已被广泛认识到其具有神经精神不良影响和导致睡眠障碍的潜力。最近,人们对整合酶抑制剂也提出了类似的担忧,尤其是多替拉韦和拉替拉韦,尽管需要进一步研究来确定这些药物在治疗系统性 HIV 方面的高疗效和有效性的情况下,是否存在与临床相关的神经精神副作用的风险。