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Predicting Efavirenz Concentrations in the Brain Tissue of HIV‐Infected Individuals and Exploring their Relationship to Neurocognitive Impairment

机译:预测感染艾滋病毒的人脑组织中依非韦伦的浓度并探讨其与神经认知障碍的关系

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摘要

Sparse data exist on the penetration of antiretrovirals into brain tissue. In this work, we present a framework to use efavirenz (EFV) pharmacokinetic (PK) data in plasma, cerebrospinal fluid (CSF), and brain tissue of eight rhesus macaques to predict brain tissue concentrations in HIV‐infected individuals. We then perform exposure‐response analysis with the model‐predicted EFV area under the concentration‐time curve (AUC) and neurocognitive scores collected from a group of 24 HIV‐infected participants. Adult rhesus macaques were dosed daily with 200 mg EFV (as part of a four‐drug regimen) for 10 days. Plasma was collected at 8 time points over 10 days and at necropsy, whereas CSF and brain tissue were collected at necropsy. In the clinical study, data were obtained from one paired plasma and CSF sample of participants prescribed EFV, and neuropsychological test evaluations were administered across 15 domains. PK modeling was performed using ADAPT version 5.0 Biomedical Simulation Resource, Los Angeles, CA) with the iterative two‐stage estimation method. An eight‐compartment model best described EFV distribution across the plasma, CSF, and brain tissue of rhesus macaques and humans. Model‐predicted median brain tissue concentrations in humans were 31 and 8,000 ng/mL, respectively. Model‐predicted brain tissue AUC was highly correlated with plasma AUC (γ = 0.99, P < 0.001) but not CSF AUC (γ = 0.34, P = 0.1) and did not show any relationship with neurocognitive scores (γ < 0.05, P > 0.05). This analysis provides an approach to estimate PK the brain tissue in order to perform PK/pharmacodynamic analyses at the target site.
机译:关于抗逆转录病毒药物渗透入脑组织的数据很少。在这项工作中,我们提出了一个框架,使用血浆,脑脊液(CSF)和八只猕猴的脑组织中的依非韦伦(EFV)药代动力学(PK)数据来预测HIV感染者的脑组织浓度。然后,我们使用浓度-时间曲线(AUC)下的模型预测的EFV区域以及从24名感染了HIV的参与者中收集的神经认知评分进行暴露-响应分析。成年恒河猴每天服用200 mg EFV(作为四药疗法的一部分),持续10天。尸检时在10天的8个时间点收集血浆,尸检时收集CSF和脑组织。在临床研究中,从一对处方EFV参与者的血浆和CSF样本中获得数据,并在15个域中进行了神经心理学测试评估。 PK建模是使用ADAPT 5.0版生物医学模拟资源(加利福尼亚州,洛杉矶)和迭代两阶段估计方法进行的。八室模型最能描述EFV在恒河猴和人的血浆,CSF和脑组织中的分布。根据模型预测,人的脑组织中位数浓度分别为31和8,000 ng / mL。模型预测的脑组织AUC与血浆AUC(γ= 0.99,P <0.001)高度相关,但与CSF AUC(γ= 0.34,P = 0.1)没有高度相关,并且与神经认知评分没有任何关系(γ<0.05,P> 0.05)。该分析提供了一种估计脑组织PK的方法,以便在目标部位进行PK /药效学分析。

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