Department of Cell Biology and Immunology, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX 76107, United States.
Department of Cell Biology and Immunology, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX 76107, United States.
Prog Neurobiol. 2017 Oct;157:117-132. doi: 10.1016/j.pneurobio.2016.04.003. Epub 2016 Apr 12.
HIV infection often causes neurological symptoms including cognitive and motor dysfunction, which have been collectively termed HIV/neuroAIDS. Neuropsychological assessment and clinical symptoms have been the primary diagnostic criteria for HIV/neuroAIDS, even for the mild cognitive and motor disorder, the most prevalent form of HIV/neuroAIDS in the era of combination antiretroviral therapy. Those performance-based assessments and symptoms are generally descriptive and do not have the sensitivity and specificity to monitor the diagnosis, progression, and treatment response of the disease when compared to objective and quantitative laboratory-based biological markers, or biomarkers. In addition, effects of demographics and comorbidities such as substance abuse, psychiatric disease, nutritional deficiencies, and co-infection on HIV/neuroAIDS could be more readily determined using biomarkers than using neuropsychological assessment and clinical symptoms. Thus, there have been great efforts in identification of HIV/neuroAIDS biomarkers over the past two decades. The need for reliable biomarkers of HIV/neuroAIDS is expected to increase as the HIV-infected population ages and their vulnerability to neurodegenerative diseases, particularly Alzheimer's disease increases. Currently, three classes of HIV/neuroAIDS biomarkers are being pursued to establish objective laboratory-based definitions of HIV-associated neurologic injury: cerebrospinal fluid biomarkers, blood biomarkers, and neuroimaging biomarkers. In this review, we will focus on the current knowledge in the field of HIV/neuroAIDS biomarker discovery.
HIV 感染常引起神经症状,包括认知和运动功能障碍,这些统称为 HIV/神经艾滋病。神经心理学评估和临床症状一直是 HIV/神经艾滋病的主要诊断标准,即使是在联合抗逆转录病毒治疗时代最常见的轻度认知和运动障碍也是如此。与客观、定量的基于实验室的生物标志物或生物标志物相比,这些基于表现的评估和症状通常是描述性的,没有敏感性和特异性来监测疾病的诊断、进展和治疗反应。此外,人口统计学和合并症(如药物滥用、精神疾病、营养缺乏和合并感染)对 HIV/神经艾滋病的影响可以通过生物标志物更容易地确定,而不是通过神经心理学评估和临床症状。因此,在过去的二十年中,人们一直在努力寻找 HIV/神经艾滋病的生物标志物。随着感染 HIV 的人群年龄的增长,他们易患神经退行性疾病(尤其是阿尔茨海默病)的风险增加,对 HIV/神经艾滋病可靠生物标志物的需求预计将会增加。目前,正在研究三类 HIV/神经艾滋病生物标志物,以建立与 HIV 相关的神经损伤的客观实验室定义:脑脊液生物标志物、血液生物标志物和神经影像学生物标志物。在这篇综述中,我们将重点介绍 HIV/神经艾滋病生物标志物发现领域的最新知识。