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在乌干达拉凯开始抗逆转录病毒治疗的 HIV 感染者的神经认知变化轨迹存在异质性。

Heterogeneity in neurocognitive change trajectories among people with HIV starting antiretroviral therapy in Rakai, Uganda.

机构信息

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.

出版信息

J Neurovirol. 2019 Dec;25(6):800-813. doi: 10.1007/s13365-019-00768-5. Epub 2019 Jun 19.

Abstract

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.

摘要

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。

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