Nichols Sharon L, Bethel James, Kapogiannis Bill G, Li Tiandong, Woods Steven P, Patton E Doyle, Ren Weijia, Thornton Sarah E, Major-Wilson Hanna O, Puga Ana M, Sleasman John W, Rudy Bret J, Wilson Craig M, Garvie Patricia A
Department of Neurosciences, University of California, 9500 Gilman Drive, #0935, La Jolla, San Diego, CA, 92093, USA.
Westat, Rockville, MD, USA.
J Neurovirol. 2016 Apr;22(2):218-30. doi: 10.1007/s13365-015-0389-0. Epub 2015 Oct 13.
Although youth living with behaviorally acquired HIV (YLWH) are at risk for cognitive impairments, the relationship of impairments to HIV and potential to improve with antiretroviral therapy (ART) are unclear. This prospective observational study was designed to examine the impact of initiation and timing of ART on neurocognitive functioning in YLWH in the Adolescent Medicine Trials Network for HIV/AIDS Interventions. Treatment naïve YLWH age 18-24 completed baseline and four additional assessments of attention/working memory, complex executive, and motor functioning over 3 years. Group 1 co-enrolled in an early ART initiation study and initiated ART at enrollment CD4 >350 (n = 56); group 2 had CD4 >350 and were not initiating ART (n = 66); group 3 initiated ART with CD4 <350 (n = 59) per standard of care treatment guidelines at the time. Treatment was de-intensified to boosted protease inhibitor monotherapy at 48 weeks for those in group 1 with suppressed viral load. Covariates included demographic, behavioral, and medical history variables. Analyses used hierarchical linear modeling. All groups showed improved performance with peak at 96 weeks in all three functional domains. Trajectories of change were not significantly associated with treatment, timing of treatment initiation, or ART de-intensification. Demographic variables and comorbidities were associated with baseline functioning but did not directly interact with change over time. In conclusion, YLWH showed improvement in neurocognitive functioning over time that may be related to practice effects and nonspecific impact of study participation. Neither improvement nor decline in functioning was associated with timing of ART initiation or therapy de-intensification.
尽管感染行为性获得性艾滋病毒的青年(YLWH)存在认知障碍风险,但这些障碍与艾滋病毒的关系以及抗逆转录病毒疗法(ART)改善认知障碍的潜力尚不清楚。这项前瞻性观察性研究旨在探讨在青少年医学艾滋病毒/艾滋病干预试验网络中,开始ART的时间和时机对YLWH神经认知功能的影响。18至24岁未接受过治疗的YLWH完成了基线评估,并在3年中对注意力/工作记忆、复杂执行功能和运动功能进行了另外四次评估。第1组同时参与了一项早期ART启动研究,并在入组时CD4>350时开始ART(n = 56);第2组CD4>350且未开始ART(n = 66);第3组按照当时的标准护理治疗指南,在CD4<350时开始ART(n = 59)。对于病毒载量得到抑制的第1组患者,在48周时将治疗强化为增强型蛋白酶抑制剂单一疗法。协变量包括人口统计学、行为学和病史变量。分析采用分层线性模型。所有组在所有三个功能领域均表现出改善,在96周时达到峰值。变化轨迹与治疗、开始治疗的时间或ART强化无关。人口统计学变量和合并症与基线功能相关,但与随时间的变化没有直接相互作用。总之,YLWH的神经认知功能随时间有所改善,这可能与练习效应和研究参与的非特异性影响有关。功能的改善或下降均与开始ART的时间或治疗强化无关。