Moschopoulos Charalampos D, Stanitsa Evangelia, Protopapas Konstantinos, Kavatha Dimitra, Papageorgiou Sokratis G, Antoniadou Anastasia, Papadopoulos Antonios
4th Department of Internal Medicine, Medical School of Athens, National and Kapodistrian University of Athens, Attikon University Hospital, 12462 Athens, Greece.
1st Department of Neurology, Medical School of Athens, National and Kapodistrian University of Athens, Eginition Hospital, 11528 Athens, Greece.
Life (Basel). 2024 Apr 15;14(4):508. doi: 10.3390/life14040508.
Combination antiretroviral treatment (cART) has revolutionized the management of human immunodeficiency virus (HIV) and has markedly improved the disease burden and life expectancy of people living with HIV. HIV enters the central nervous system (CNS) early in the course of infection, establishes latency, and produces a pro-inflammatory milieu that may affect cognitive functions, even in the cART era. Whereas severe forms of neurocognitive impairment (NCI) such as HIV-associated dementia have declined over the last decades, milder forms have become more prevalent, are commonly multifactorial, and are associated with comorbidity burdens, mental health, cART neurotoxicity, and ageing. Since 2007, the Frascati criteria have been used to characterize and classify HIV-associated neurocognitive disorders (HAND) into three stages, namely asymptomatic neurocognitive impairment (ANI), mild neurocognitive disorder (MND), and HIV-associated dementia (HAD). These criteria are based on a comprehensive neuropsychological assessment that presupposes the availability of validated, demographically adjusted, and normative population data. Novel neuroimaging modalities and biomarkers have been proposed in order to complement NCI assessments, elucidate neuropathogenic mechanisms, and support HIV-associated NCI diagnosis, monitoring, and prognosis. By integrating neuropsychological assessments with biomarkers and neuroimaging into a holistic care approach, clinicians can enhance diagnostic accuracy, prognosis, and patient outcomes. This review interrogates the value of these modes of assessment and proposes a unified approach to NCI diagnosis.
联合抗逆转录病毒治疗(cART)彻底改变了人类免疫缺陷病毒(HIV)的管理方式,并显著减轻了HIV感染者的疾病负担,延长了他们的预期寿命。在感染过程的早期,HIV就会进入中枢神经系统(CNS),建立潜伏状态,并产生一种促炎环境,即使在cART时代,这种环境也可能影响认知功能。在过去几十年里,诸如HIV相关痴呆等严重形式的神经认知障碍(NCI)有所减少,但较轻形式的神经认知障碍却变得更加普遍,通常是多因素导致的,并且与合并症负担、心理健康、cART神经毒性和衰老有关。自2007年以来,弗拉斯卡蒂标准一直被用于将HIV相关神经认知障碍(HAND)分为三个阶段进行特征描述和分类,即无症状神经认知障碍(ANI)、轻度神经认知障碍(MND)和HIV相关痴呆(HAD)。这些标准基于全面的神经心理学评估,而这又预先假定有经过验证的、根据人口统计学调整的和标准化的人群数据。为了补充NCI评估、阐明神经致病机制并支持HIV相关NCI的诊断、监测和预后,人们提出了新的神经影像学方法和生物标志物。通过将神经心理学评估与生物标志物和神经影像学整合到整体护理方法中,临床医生可以提高诊断准确性、改善预后并提升患者治疗效果。本综述探讨了这些评估方式的价值,并提出了一种统一的NCI诊断方法。