Luckett Patrick H, Paul Robert H, Hannon Kayla, Lee John J, Shimony Joshua S, Meeker Karin L, Cooley Sarah A, Boerwinkle Anna H, Ances Beau M
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri.
Department of Psychological Sciences, University of Missouri Saint Louis, St. Louis, Missouri; and.
J Acquir Immune Defic Syndr. 2021 Dec 1;88(4):414-419. doi: 10.1097/QAI.0000000000002783.
The relationship between HIV infection, the functional organization of the brain, cognitive impairment, and aging remains poorly understood. Understanding disease progression over the life span is vital for the care of people living with HIV (PLWH).
Virologically suppressed PLWH (n = 297) on combination antiretroviral therapy and 1509 HIV-uninfected healthy controls were evaluated. PLWH were further classified as cognitively normal (CN) or cognitively impaired (CI) based on neuropsychological testing.
Feature selection identified resting-state networks (RSNs) that predicted HIV status and cognitive status within specific age bins (younger than 35 years, 35-55 years, and older than 55 years). Deep learning models generated voxelwise maps of RSNs to identify regional differences.
Salience (SAL) and parietal memory networks (PMNs) differentiated individuals by HIV status. When comparing controls with PLWH CN, the PMN and SAL had the strongest predictive strength across all ages. When comparing controls with PLWH CI, the SAL, PMN, and frontal parietal network (FPN) were the best predictors. When comparing PLWH CN with PLWH CI, the SAL, FPN, basal ganglia, and ventral attention were the strongest predictors. Only minor variability in predictive strength was observed with aging. Anatomically, differences in RSN topology occurred primarily in the dorsal and rostral lateral prefrontal cortex, cingulate, and caudate.
Machine learning identified RSNs that classified individuals by HIV status and cognitive status. The PMN and SAL were sensitive for discriminating HIV status, with involvement of FPN occurring with cognitive impairment. Minor differences in RSN predictive strength were observed by age. These results suggest that specific RSNs are affected by HIV, aging, and HIV-associated cognitive impairment.
人们对HIV感染、大脑功能组织、认知障碍和衰老之间的关系仍知之甚少。了解疾病在整个生命周期中的进展对于护理HIV感染者(PLWH)至关重要。
对接受联合抗逆转录病毒治疗的病毒学抑制的PLWH(n = 297)和1509名未感染HIV的健康对照进行了评估。根据神经心理学测试,PLWH被进一步分为认知正常(CN)或认知受损(CI)。
特征选择确定了在特定年龄组(35岁以下、35 - 55岁和55岁以上)中预测HIV状态和认知状态的静息态网络(RSN)。深度学习模型生成了RSN的体素图,以识别区域差异。
显著性(SAL)和顶叶记忆网络(PMN)根据HIV状态区分个体。将对照组与PLWH CN进行比较时,PMN和SAL在所有年龄段都具有最强的预测强度。将对照组与PLWH CI进行比较时,SAL、PMN和额顶叶网络(FPN)是最佳预测指标。将PLWH CN与PLWH CI进行比较时,SAL、FPN、基底神经节和腹侧注意是最强的预测指标。随着年龄增长,预测强度仅观察到微小变化。在解剖学上,RSN拓扑结构的差异主要发生在背侧和喙侧外侧前额叶皮质、扣带回和尾状核。
机器学习确定了可根据HIV状态和认知状态对个体进行分类的RSN。PMN和SAL对区分HIV状态敏感,认知障碍时FPN会受累。按年龄观察到RSN预测强度的微小差异。这些结果表明特定的RSN受HIV、衰老和HIV相关认知障碍的影响。