A4 研究中认知功能指数的项目级响应与 Tau 病理学和海马体积的关系

idris demirsoy, Ali Ezzati, Bhargav Nallapu, Elham Ghanbare, Babak Khorsand
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引用次数: 0

摘要

背景:阿尔茨海默病(AD)有一个漫长的无症状临床前期阶段,在此期间,患者可能会出现β-淀粉样蛋白(Aβ)病理和tau缠结等病理症状,但没有明显的客观认知障碍。主观认知障碍报告可为早期了解个人认知功能提供有价值的信息,并可作为认知功能衰退早期阶段的指标:目的:研究参与者和研究伙伴对认知功能指数(CFI)的项目级反应与tau病理学和调整后海马体积(HVa)的关联:参与者为339名认知功能未受损、Aβ阳性、参加了抗淀粉样蛋白无症状阿尔茨海默氏症(A4)研究并接受了tau-PET成像的个体。参与者及其研究伙伴使用 15 项 CFI 问卷对过去一年中认知和功能的主观变化进行评估。针对每个 CFI 项目,研究了 tau、HVa 和 CFI 报告之间的关系。结果显示参与者平均年龄为 72.38 (SD = 4.87)岁,58.1% 为女性,23.6% 为 tau 阳性。在三个 CFI 项目中,tauMTL 越高与参与者的衰退报告显著相关,这三个项目包括依赖书面笔记、因记忆问题看医生以及在导航时感到迷失方向。较高的 tauMTL 与研究伙伴在两个不同项目上报告的记忆力下降有关:需要他人帮助才能记住约会/事件以及询问相同的问题。此外,HVa 与参与者的驾驶挑战和研究伙伴明显的记忆力下降有关:我们的研究表明,CFI特定项目的早期变化与Aβ+参与者较高的tauMTL和较低的HVa有关。不同的CFI项目与参与者和研究伙伴的tau和海马体积相关,突出了这两个视角的重要性。
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Association of Item-Level Responses to Cognitive Function Index with Tau Pathology and Hippocampal volume in The A4 Study
Background: Alzheimer's Disease (AD) has a lengthy asymptomatic preclinical phase during which individuals may show pathological signs like β-amyloid (Aβ) pathology and tau tangles without noticeable objective cognitive impairments. Subjective cognitive impairment reports may offer valuable and early insights into individuals' cognitive functioning and serve as indicators of early stages of cognitive decline. Objective: To investigate the associations of the item-level response to Cognitive Function Index (CFI) by participant and study partner with tau pathology and adjusted hippocampal volume (HVa). Method: Participants were 339 cognitively unimpaired, Aβ positive, individuals enrolled in the Anti-Amyloid Asymptomatic Alzheimer's (A4) Study who underwent tau-PET imaging. Participants and their study partners assessed subjective changes in cognition and function over the past year using the 15-item CFI questionnaire. For each CFI item, the relationship among tau, HVa, and CFI reports was investigated. Result: Participants were on average 72.38 (SD = 4.87) years old, 58.1% were female, and 23.6% were tau positive. Higher tauMTL was significantly associated with participant report of decline on three CFI items including depending on written notes, seeing a doctor for memory concern, and feeling lost while navigating. Higher tauMTL was associated with study partner report of decline on two different items: needing help from others to remember appointments/occasions and asking same questions. Additionally, HVa was linked to challenges with driving for participants and noticeable memory decline for study partners. Conclusion: We showed that early changes reported on specific items of the CFI are associated with higher tauMTL and lower HVa in Aβ+ participants. Different CFI items were associated with tau and hippocampal volume for participants and study partners, highlighting the importance of both perspective.
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