Kamkwalala Asante R, Matthews Avery, Garg Ankita, Roy Upal, Ma Qing, Karris Maile, Sundermann Erin, Ellis Ronald J, Riggs Patricia K, Trunfio Mattia, Blanchard Jennifer, Moore David J, Rubin Leah H, Letendre Scott L
Department of Neurology, Johns Hopkins University, Baltimore, Maryland, USA.
Department of Psychiatry, University of Texas Health Science Center, San Antonio, Texas, USA.
Clin Infect Dis. 2025 Apr 30;80(4):871-880. doi: 10.1093/cid/ciae518.
Alterations in brain function and structure, such as depression and neurocognitive impairment, continue to occur in people with human immunodeficiency virus (HIV, PWH) taking suppressive antiretroviral therapy (ART). The lifespan of PWH has improved but the healthspan remains worse than people without HIV, in part because of aging-related diseases. As a result, polypharmacy is common and increases the risk of drug-drug interactions and adverse reactions.
This cross-sectional project investigated the relationship between 7 medication-related metrics (including anticholinergic burden), depressive symptoms, and neurocognitive performance in 491 PWH at a single center in the United States. All participants were taking ART and had plasma HIV RNA ≤ 200 copies/mL.
Participants had taken ART for a mean of 6.5 years, and most (57.6%) had CD4+ T-cells >500/µL. All 7 medication-related metrics were associated with worse global neurocognitive performance (P value <.0001 to .0087). Multivariable models confirmed that higher anticholinergic burden (P = .040) and use of benzodiazepines (P = .033), antidepressants (P = .0011), and more total medications (P = .059) were associated with more depressive symptoms (model P < .0001). Use of benzodiazepines (P = .0024) and opiates (P = .043) along with higher anticholinergic burden (P = .066) were also associated with worse neurocognitive performance. Benzodiazepine use was associated with worse performance in all domains and opiate use was associated with worse performance in processing speed, motor function, executive function, and working memory.
Use of benzodiazepines, opiates, and anticholinergic drugs contribute to cognitive and mood disorders in PWH. When possible, modifying or deprescribing medications may be beneficial.
在接受抑制性抗逆转录病毒疗法(ART)的人类免疫缺陷病毒(HIV)感染者(PWH)中,大脑功能和结构的改变,如抑郁和神经认知障碍,仍在持续出现。PWH的寿命有所延长,但健康寿命仍比未感染HIV的人差,部分原因是与衰老相关的疾病。因此,联合用药很常见,这增加了药物相互作用和不良反应的风险。
这个横断面项目在美国的一个单一中心调查了491名PWH中7种与药物相关的指标(包括抗胆碱能负担)、抑郁症状和神经认知表现之间的关系。所有参与者都在接受ART治疗,血浆HIV RNA≤200拷贝/毫升。
参与者接受ART的平均时间为6.5年,大多数(57.6%)的CD4 + T细胞>500/μL。所有7种与药物相关的指标都与较差的整体神经认知表现相关(P值<.0001至.0087)。多变量模型证实,较高的抗胆碱能负担(P = .040)以及使用苯二氮䓬类药物(P = .033)、抗抑郁药(P = .0011)和更多的总用药量(P = .059)与更多的抑郁症状相关(模型P <.0001)。使用苯二氮䓬类药物(P = .0024)和阿片类药物(P = .043)以及较高的抗胆碱能负担(P = .066)也与较差的神经认知表现相关。使用苯二氮䓬类药物与所有领域的较差表现相关,使用阿片类药物与处理速度、运动功能、执行功能和工作记忆方面的较差表现相关。
使用苯二氮䓬类药物、阿片类药物和抗胆碱能药物会导致PWH出现认知和情绪障碍。尽可能调整用药或减少用药可能有益。