Functional Connectivity in Virally Suppressed Patients with HIV-Associated Neurocognitive Disorder: A Resting-State Analysis

被引:39
作者
Chaganti, J. R. [1 ]
Heinecke, A. [3 ]
Gates, T. M. [4 ]
Moffat, K. J. [1 ]
Brew, B. J. [2 ,5 ]
机构
[1] St Vincents Hosp, Dept Radiol, Sydney, NSW, Australia
[2] St Vincents Hosp, Dept Neurol, Sydney, NSW, Australia
[3] Brain Innovat BV, Maastricht, Netherlands
[4] Univ New South Wales, St Vincents Ctr Appl Med Res, Dept Neurol, Clin Res Program, Sydney, NSW, Australia
[5] Univ New South Wales, St Vincents Ctr Appl Med Res, Peter Duncan Neurosci Unit, Neurosci Program, Sydney, NSW, Australia
关键词
ACTIVE ANTIRETROVIRAL THERAPY; HUMAN-IMMUNODEFICIENCY-VIRUS; AIDS DEMENTIA COMPLEX; INFECTION; ERA; IMPAIRMENT; ACTIVATION; COGNITION; NETWORK; DISEASE;
D O I
10.3174/ajnr.A5246
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: HIV-associated neurocognitive disorder still occurs despite virally suppressive combination antiretroviral therapy. In the pre-combination antiretroviral era and in patients without HIV suppression, HIV-associated neurocognitive disorder was caused by synaptodendritic injury resulting in impairment of neural networks, characterized by decreased attention, psychomotor slowing, and working memory deficits. Whether similar pathogenesis is true for HIV-associated neurocognitive disorder in the context of viral suppression is not clear. Resting-state fMRI has been shown to be efficient in detecting impaired neural networks in various neurologic illnesses. This pilot study aimed to assess resting-state functional connectivity of the brain in patients with active HIV-associated neurocognitive disorder in the context of HIV viral suppression in both blood and CSF. MATERIALS AND METHODS: Eighteen patients with active HIV-associated neurocognitive disorder (recent diagnosis with progressing symptoms) on combination antiretroviral therapy with viral suppression in both blood and CSF and 9 demographically matched control subjects underwent resting-state functional MR imaging. The connectivity in the 6 known neural networks was assessed. To localize significant ROIs within the HIV and control group, we performed a seed-based correlation for each known resting-state network. RESULTS: There were significant group differences between the control and HIV-associated neurocognitive disorder groups in the salience (0.26 versus 0.14, t = 2.6978, df = 25, P = .0123) and executive networks (0.52 versus 0.32, t = 2.2372, df = 25, P = .034). The covariate analysis with neuropsychological scores yielded statistically significant correlations in all 6 studied functional networks, with the most conspicuous correlation in salience networks. CONCLUSIONS: Active HIV-associated neurocognitive disorder in virally suppressed patients is associated with significantly decreased connectivity in the salience and executive networks, thereby making it potentially useful as a biomarker.
引用
收藏
页码:1623 / 1629
页数:7
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