Kelly Sophie H, Nightingale Sam, Gupta Ravindra K, Collier Dami A
Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, UK.
Department of Medicine, University of Cambridge, Cambridge CB2 1TN, UK.
Trop Med Infect Dis. 2025 Feb 5;10(2):45. doi: 10.3390/tropicalmed10020045.
Neurocognitive impairment is an important cause of HIV-associated morbidity. The advent of antiretroviral therapy (ART) has shifted the spectrum of HIV-associated cognitive impairment from HIV-associated dementia to milder forms of cognitive impairment. Independent replication of HIV within the central nervous system in those on effective ART with peripheral suppression is a recognised phenomenon known as cerebrospinal fluid (CSF) HIV RNA escape. CSF HIV RNA escape is independently associated with neurocognitive impairment but has also been detected in asymptomatic persons with HIV. The current consensus for management of CSF HIV RNA escape is based on expert opinion rather than empirical evidence. The current evidence suggests having a low threshold to investigate for CSF HIV RNA escape and optimising ART based on resistance profiles. The use of central nervous system (CNS) penetration effectiveness scores is no longer recommended. The evidence for statins, SSRIs, minocycline, lithium and valproate is limited to small-scale studies. There are potential new developments in the form of nanoparticles, Janus Kinase inhibitors and latency reversal agents.
神经认知障碍是与HIV相关发病的重要原因。抗逆转录病毒疗法(ART)的出现已将HIV相关认知障碍的范围从HIV相关痴呆转变为较轻形式的认知障碍。在接受有效ART且外周病毒得到抑制的人群中,HIV在中枢神经系统内的独立复制是一种公认的现象,称为脑脊液(CSF)HIV RNA逃逸。CSF HIV RNA逃逸与神经认知障碍独立相关,但在无症状HIV感染者中也已检测到。目前对于CSF HIV RNA逃逸管理的共识基于专家意见而非实证证据。当前证据表明,对于CSF HIV RNA逃逸的调查阈值应较低,并根据耐药谱优化ART。不再推荐使用中枢神经系统(CNS)渗透有效性评分。他汀类药物、选择性5-羟色胺再摄取抑制剂(SSRI)、米诺环素、锂盐和丙戊酸盐的证据仅限于小规模研究。纳米颗粒、Janus激酶抑制剂和潜伏逆转剂等形式可能会有新的进展。