Department of Neurology, Johns Hopkins University School of Medicine, 600 N. Wolfe Street/Meyer 6-113, Baltimore, MD, 21287-7613, USA.
Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Neurovirol. 2019 Dec;25(6):800-813. doi: 10.1007/s13365-019-00768-5. Epub 2019 Jun 19.
Considerable heterogeneity exists in patterns of neurocognitive change in people with HIV (PWH). We examined heterogeneity in neurocognitive change trajectories from HIV diagnosis to 1-2 years post-antiretroviral therapy (ART). In an observational cohort study in Rakai, Uganda, 312 PWH completed a neuropsychological (NP) test battery at two-time points (ART-naïve, 1-2 years post-ART initiation). All NP outcomes were used in a latent profile analysis to identify subgroups of PWH with similar ART-related neurocognitive change profiles. In a subset, we examined subgroup differences pre-ART on cytokine and neurodegenerative biomarkers CSF levels. We identified four ART-related change subgroups: (1) decline-only (learning, memory, fluency, processing speed, and attention measures), (2) mixed (improvements in learning and memory but declines in attention and executive function measures), (3) no-change, or (4) improvement-only (learning, memory, and attention measures). ART-related NP outcomes that are most likely to change included learning, memory, and attention. Motor function measures were unchanged. Subgroups differed on eight of 34 pre-ART biomarker levels including interleukin (IL)-1β, IL-6, IL-13, interferon-γ, macrophage inflammatory protein-1β, matrix metalloproteinase (MMP)-3, MMP-10, and platelet-derived growth factor-AA. The improvement-only and mixed subgroups showed lower levels on these markers versus the no-change subgroup. These findings provide support for the need to disentangle heterogeneity in ART-related neurocognitive changes, to focus on higher-order cognitive processes (learning, memory, attention) as they were most malleable to change, and to better understand why motor function remained unchanged despite ART treatment. Group differences in pre-ART CSF levels provide preliminary evidence of biological plausibility of neurocognitive phenotyping.
HIV 感染者(PWH)的神经认知变化模式存在很大的异质性。我们研究了从 HIV 诊断到抗逆转录病毒治疗(ART)后 1-2 年期间神经认知变化轨迹的异质性。在乌干达拉凯的一项观察性队列研究中,312 名 PWH 在两个时间点完成了神经心理测试(ART 初治,ART 开始后 1-2 年)。所有神经认知测试结果均用于潜在剖面分析,以确定具有相似 ART 相关神经认知变化特征的 PWH 亚组。在一个亚组中,我们检查了亚组在 ART 前细胞因子和神经退行性生物标志物 CSF 水平上的差异。我们确定了四个与 ART 相关的变化亚组:(1)仅下降(学习、记忆、流畅性、处理速度和注意力指标),(2)混合(学习和记忆改善,但注意力和执行功能指标下降),(3)无变化,或(4)仅改善(学习、记忆和注意力指标)。最有可能发生变化的与 ART 相关的神经认知测试结果包括学习、记忆和注意力。运动功能指标无变化。亚组在 34 个 ART 前生物标志物水平中的 8 个方面存在差异,包括白细胞介素(IL)-1β、IL-6、IL-13、干扰素-γ、巨噬细胞炎症蛋白-1β、基质金属蛋白酶(MMP)-3、MMP-10 和血小板衍生生长因子-AA。与无变化亚组相比,仅改善和混合亚组这些标志物的水平较低。这些发现为需要分解与 ART 相关的神经认知变化的异质性提供了支持,需要关注更高级别的认知过程(学习、记忆、注意力),因为它们最容易发生变化,并更好地理解为什么尽管进行了 ART 治疗,但运动功能仍未改变。ART 前 CSF 水平的组间差异为神经认知表型提供了初步的生物学合理性证据。