Chaganti J R, Heinecke A, Gates T M, Moffat K J, Brew B J
From the Departments of Radiology (J.R.C., K.J.M.)
Brain Innovation B.V. (A.H.), Maastricht, the Netherlands.
AJNR Am J Neuroradiol. 2017 Aug;38(8):1623-1629. doi: 10.3174/ajnr.A5246. Epub 2017 Jun 8.
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.
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.
There were significant group differences between the control and HIV-associated neurocognitive disorder groups in the salience (0.26 versus 0.14, = 2.6978, = 25, = .0123) and executive networks (0.52 versus 0.32, = 2.2372, = 25, = .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.
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.
尽管采用了具有病毒抑制作用的联合抗逆转录病毒疗法,但HIV相关神经认知障碍仍会有发生。在联合抗逆转录病毒疗法之前的时代以及未实现HIV抑制的患者中,HIV相关神经认知障碍是由突触树突损伤导致神经网络受损引起的,其特征为注意力下降、精神运动迟缓以及工作记忆缺陷。在病毒抑制的情况下,HIV相关神经认知障碍是否具有类似的发病机制尚不清楚。静息态功能磁共振成像已被证明在检测各种神经系统疾病中受损的神经网络方面具有有效性。这项初步研究旨在评估在血液和脑脊液中均实现HIV病毒抑制的情况下,活动性HIV相关神经认知障碍患者大脑的静息态功能连接。
18例接受联合抗逆转录病毒疗法且血液和脑脊液中病毒均得到抑制的活动性HIV相关神经认知障碍患者(近期诊断且症状进展)以及9名人口统计学匹配的对照受试者接受了静息态功能磁共振成像检查。评估了6个已知神经网络中的连接性。为了在HIV组和对照组中定位显著的感兴趣区域(ROI),我们对每个已知的静息态网络进行了基于种子点的相关性分析。
在显著性网络(0.26对0.14,t = 2.6978,df = 25,P = 0.0123)和执行网络(0.52对0.32,t = 2.2372,df = 25,P = 0.034)方面,对照组与HIV相关神经认知障碍组之间存在显著的组间差异。对神经心理学评分进行的协变量分析在所有6个研究的功能网络中均产生了具有统计学意义的相关性,其中在显著性网络中的相关性最为明显。
病毒抑制患者中的活动性HIV相关神经认知障碍与显著性网络和执行网络中的连接性显著降低相关,因此其有可能作为一种生物标志物。