Dubbelman Mark A, Elias Uri, Palmer Phebe, Dafni-Merom Amnon, Gazit Lidor, Udeogu Onyinye J, Wang Sharon, Papp Kathryn V, Amariglio Rebecca E, Arzy Shahar, Marshall Gad A
Department of Neurology, Center for Alzheimer Research and Treatment, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
J Alzheimers Dis. 2025 Apr 23:13872877251334781. doi: 10.1177/13872877251334781.
BackgroundImpairments in orientation in space, time, and person occur frequently in Alzheimer's disease (AD) dementia. Subtle changes in orientation may arise in preclinical and prodromal disease stages. Thus, assessing orientation may help identify those on a trajectory toward AD dementia.ObjectiveTo investigate how orientation, measured using a novel artificial intelligence-based paradigm, relates to AD biomarkers (amyloid and tau) in cognitively unimpaired older adults.MethodsUsing an automated chatbot, 53 cognitively unimpaired participants (74.0 ± 5.5 years; 60% female) provided details about memories and relationships, recognition of historical event dates, and geographical locations. These details were then used to assess orientation to space, time, and person. For each domain separately, orientation accuracy was calculated by dividing the number of correct responses by response time. All participants underwent Pittsburgh compound-B (amyloid) and flortaucipir (tau) positron emission tomography. We analyzed the relationship between performance on the three orientation domains and retrosplenial, precuneus, neocortical, and medial temporal tau, and global amyloid.ResultsHigher retrosplenial and precuneus tau burden were associated with worse temporal orientation (β = -0.32, 95% confidence interval [95%CI] = [-0.59, -0.05] and β = -0.29, 95%CI = [-0.57, -0.01], respectively). Spatial or social orientation were not associated with amyloid or tau.ConclusionsThese results suggest that impaired temporal orientation is related to AD pathological processes, even before the onset of overt cognitive impairment, and may infer a role for personalized assessment of orientation in early diagnosis of AD.
背景
空间、时间和人物定向障碍在阿尔茨海默病(AD)痴呆中很常见。在临床前和前驱疾病阶段可能会出现定向的细微变化。因此,评估定向可能有助于识别处于AD痴呆轨迹上的人群。
目的
研究使用基于人工智能的新型范式测量的定向与认知未受损的老年人的AD生物标志物(淀粉样蛋白和tau蛋白)之间的关系。
方法
通过一个自动化聊天机器人,53名认知未受损的参与者(74.0±5.5岁;60%为女性)提供了有关记忆和人际关系、历史事件日期的识别以及地理位置的详细信息。然后利用这些详细信息评估空间、时间和人物定向。对于每个领域,分别通过将正确回答的数量除以回答时间来计算定向准确性。所有参与者均接受了匹兹堡化合物B(淀粉样蛋白)和氟代脱氧葡萄糖(tau蛋白)正电子发射断层扫描。我们分析了三个定向领域的表现与扣带回后回、楔前叶、新皮质和内侧颞叶tau蛋白以及整体淀粉样蛋白之间的关系。
结果
扣带回后回和楔前叶较高的tau蛋白负荷与较差的时间定向相关(β=-0.32,95%置信区间[95%CI]=[-0.59,-0.05];β=-0.29,95%CI=[-0.57,-0.01])。空间或社会定向与淀粉样蛋白或tau蛋白无关。
结论
这些结果表明,即使在明显的认知障碍发作之前,时间定向受损也与AD病理过程相关,并且可能推断出定向的个性化评估在AD早期诊断中的作用。