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病毒抑制的HIV感染者的认知变化轨迹表明疾病活动的高患病率。

Cognitive change trajectories in virally suppressed HIV-infected individuals indicate high prevalence of disease activity.

作者信息

Gott Chloe, Gates Thomas, Dermody Nadene, Brew Bruce J, Cysique Lucette A

机构信息

Psychology Department, Macquarie University, Sydney, NSW, Australia.

Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.

出版信息

PLoS One. 2017 Mar 6;12(3):e0171887. doi: 10.1371/journal.pone.0171887. eCollection 2017.

DOI:10.1371/journal.pone.0171887
PMID:28264037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5338778/
Abstract

BACKGROUND

The longitudinal rate and profile of cognitive decline in persons with stable, treated, and virally suppressed HIV infection is not established. To address this question, the current study quantifies the rate of cognitive decline in a cohort of virally suppressed HIV+ persons using clinically relevant definitions of decline, and determine cognitive trajectories taking into account historical and baseline HAND status.

METHODS

Ninety-six HIV+ (clinically stable and virally undetectable) and 44 demographically comparable HIV- participants underwent standard neuropsychological testing at baseline and 18-months follow-up. We described clinically relevant cognitive trajectories based on standard definitions of historical and baseline HAND status and cognitive decline. Historical, moderate to severe HAND was formally diagnosed at the start of the cART era in 15/96 participants based on clinical neurological and neuropsychological assessment. The same standard of care has been applied to all participants at St. Vincent's Hospital Infectious Disease Department for the duration of their HIV infection (median of 20 years).

RESULTS

Relative to HIV- controls (4.5%), 14% of HIV+ participants declined (p = .11), they also scored significantly lower on the global change score (p = .03), processing speed (p = .02), and mental flexibility/inhibition (p = .02) domains. Having HAND at baseline significantly predicted cognitive decline at follow up (p = .005). We determined seven clinically relevant cognitive trajectories taking into account whether participant has a history of HAND prior to study entry (yes/no); their results on the baseline assessment (baseline impairment: yes/no) and their results on the 18-month follow up (decline or stable) which in order of prevalence were: 1) No HAND history, no baseline impairment, 18-month follow-up stable (39%), 2) No HAND history, baseline impairment, 18-month follow-up stable (35%), 3) History of HAND; baseline impairment, 18-month follow-up stable (9%) 4) No history of HAND, baseline impairment, 18-month follow-up decline (7%), 5) History of HAND, no baseline impairment, 18-month follow-up stable (3%), 6) No HAND history, no baseline impairment, 18-month follow-up decline (3%) 7) History of HAND, baseline impairment, 18-month follow-up decline (3%). There was no relationship between cognitive decline (taking into account historical and baseline HAND) and traditional HIV disease biomarkers.

CONCLUSIONS

Despite long-term viral suppression, we found mostly subclinical levels of decline in psychomotor speed and executive functioning (mental flexibility and cognitive inhibition); well-established markers of HAND progression. Moreover, 57% of our cohort is undergoing slow evolution of their disease, challenging the notion of prevalent neurocognitive stability in virally suppressed HIV infection.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/005f33f1201e/pone.0171887.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/4e3e368a3d93/pone.0171887.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/afec808cc172/pone.0171887.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/005f33f1201e/pone.0171887.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/4e3e368a3d93/pone.0171887.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/afec808cc172/pone.0171887.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b57f/5338778/005f33f1201e/pone.0171887.g003.jpg
摘要

背景

在病情稳定、接受治疗且病毒得到抑制的HIV感染者中,认知功能下降的纵向速率和特征尚未明确。为解决这一问题,本研究使用临床上相关的衰退定义,对一组病毒得到抑制的HIV阳性者的认知衰退速率进行量化,并在考虑既往和基线期的HIV相关神经认知障碍(HAND)状态的情况下确定认知轨迹。

方法

96名HIV阳性者(临床稳定且病毒载量不可检测)和44名人口统计学特征匹配的HIV阴性参与者在基线期和18个月随访时接受了标准神经心理学测试。我们根据既往和基线期HAND状态以及认知衰退的标准定义,描述了临床上相关的认知轨迹。在cART时代开始时,根据临床神经学和神经心理学评估,15/96名参与者被正式诊断为既往中重度HAND。在圣文森特医院传染病科,所有参与者在其HIV感染期间(中位数为20年)均接受相同的标准治疗。

结果

相对于HIV阴性对照者(4.5%),14%的HIV阳性参与者出现认知衰退(p = 0.11),他们在整体变化评分(p = 0.03)、处理速度(p = 0.02)和心理灵活性/抑制(p = 0.02)领域的得分也显著更低。基线期存在HAND显著预测随访时的认知衰退(p = 0.005)。我们确定了七条临床上相关的认知轨迹,考虑参与者在研究入组前是否有HAND病史(是/否);他们在基线评估中的结果(基线损伤:是/否)以及他们在18个月随访时的结果(衰退或稳定),按患病率排序依次为:1)无HAND病史,无基线损伤,18个月随访稳定(39%),2)无HAND病史,基线损伤,18个月随访稳定(35%),3)有HAND病史;基线损伤,18个月随访稳定(9%),4)无HAND病史,基线损伤,18个月随访衰退(7%),5)有HAND病史,无基线损伤,18个月随访稳定(3%),6)无HAND病史,无基线损伤,18个月随访衰退(3%),7)有HAND病史,基线损伤,18个月随访衰退(3%)。认知衰退(考虑既往和基线期HAND)与传统HIV疾病生物标志物之间无关联。

结论

尽管病毒长期得到抑制,但我们发现心理运动速度和执行功能(心理灵活性和认知抑制)大多处于亚临床水平的衰退;这些是HAND进展的明确标志。此外,我们队列中的57%正在经历疾病的缓慢演变,这对病毒得到抑制的HIV感染中普遍存在神经认知稳定性的观点提出了挑战。

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