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Maraviroc-intensified combined antiretroviral therapy improves cognition in virally suppressed HIV-associated neurocognitive disorder

机译:Maraviroc强化的联合抗逆转录病毒疗法可改善被病毒抑制的HIV相关神经认知障碍的认知

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Objective:To investigate whether intensification of combined antiretroviral therapy (cART) with the CC chemokine receptor type 5 (CCR5) entry inhibitor maraviroc leads to improvement in global neurocognitive functioning in virally suppressed men with HIV-associated neurocognitive disorder (HAND).Design:Prospective, double observer-blinded, open-label pilot randomized-controlled trial. Participants were randomized to remain on their existing cART regimen (control arm; n=8) or receive maraviroc-intensification (maraviroc arm; n=9).Methods:Participants completed a five-domain neuropsychological battery at baseline, 6- and 12-month visits. Raw scores were transformed into age-corrected z-scores and averaged into a global z-score. Single voxel (H-1)-magnetic resonance spectroscopy (MRS) major cerebral metabolite concentrations were collected at baseline and 12 months in the basal ganglia and frontal white matter and quantified using jMRUI. Neuroinflammatory biomarkers cerebrospinal fluid neopterin and (2)-microglobulin were also measured.Results:Fourteen of the 17 participants completed the study: nine maraviroc arm and five control. We found medium to large effect sizes in favour of improved global neurocognitive performance in the maraviroc arm over time {armtime interaction: P<0.05; 6 month: [=-0.10, standard error(SE)=0.04, 90% confidence interval(90%CI)=-0.18,.03; P<0.03] yielding a large effect-size d=0.77 (90%CI=-0.19,1.71); 12 month: [=-0.01; SE=0.05; 90%CI=-0.09, 0.06; P<0.77] yielding a moderate effect-size d=0.55 (90%CI=-0.47,1.55)}. No treatment-related changes were detected for H-1-MRS metabolites or cerebrospinal fluid biomarkers.Conclusion:This pilot study provides feasibility, tolerability, proof-of-concept and preliminary evidence for clinically relevant neurocognitive improvement in cART enhancement with maraviroc in virally suppressed HAND patients. Lack of concomitant brain metabolite and biomarker change may be related to complex dynamics of brain repair. Copyright (C) 2016 Wolters Kluwer Health, Inc. All rights reserved.
机译:目的:研究联合应用5型CC趋化因子受体(CCR5)进入抑制剂maraviroc的抗逆转录病毒疗法(cART)的使用是否能改善被病毒抑制的HIV相关神经认知障碍(HAND)患者的整体神经认知功能。 ,双观察者盲,开放标签的先导随机对照试验。参加者被随机分配以保留其现有的cART方案(对照组; n = 8)或接受马拉维罗强化治疗(maraviroc组; n = 9)。方法:参加者在基线,6-和12-时完成了五域神经心理训练。每月访问。原始分数将转换为年龄校正的Z分数,然后平均为整体Z分数。在基线和12个月时,在基底神经节和额叶白质中收集了单一体素(H-1)磁共振波谱(MRS)的主要脑代谢物浓度,并使用jMRUI进行了定量。还测量了脑脊液新蝶呤和(2)-微球蛋白等神经炎性生物标志物。结果:17名参与者中有14名完成了这项研究:9名马拉维罗臂和5名对照。我们发现,随着时间的推移,中大型效应有利于改善maraviroc臂的整体神经认知功能{臂间相互作用:P <0.05; 6个月:[=-0.10,标准误(SE)= 0.04,90%置信区间(90%CI)=-0.18,.03; P <0.03]产生大的效应大小d = 0.77(90%CI = -0.19,1.71); 12个月:[=-0.01; SE = 0.05; 90%CI = -0.09,0.06; P <0.77]产生适度的效应大小d = 0.55(90%CI = -0.47,1.55)}。没有发现H-1-MRS代谢产物或脑脊液生物标志物的治疗相关变化。结论:该初步研究为在病毒抑制下用maraviroc增强cART的临床相关神经认知改善提供了可行性,耐受性,概念验证和初步证据。 HAND患者。缺乏伴随的脑代谢物和生物标志物的变化可能与复杂的脑修复动力学有关。版权所有(C)2016 Wolters Kluwer Health,Inc.保留所有权利。

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