疾病
神经影像学
早发性阿尔茨海默病
医学
神经科学
认知
阿尔茨海默病神经影像学倡议
基线(sea)
淀粉样蛋白(真菌学)
阿尔茨海默病
内科学
心理学
匹兹堡化合物B
认知障碍
正电子发射断层摄影术
临床疾病
纵向研究
退行性疾病
病态的
τ蛋白
神经功能成像
发病年龄
背景(考古学)
痴呆
认知功能衰退
临床试验
中枢神经系统疾病
肿瘤科
大脑定位
相关性
作者
Konstantinos Chiotis,Ganna Blazhenets,David N. Soleimani‐Meigooni,Paul S. S Aisen,Alinda N. Amuiri,Alireza Atri,Laurel A. Beckett,Michael J. Brickhouse,David Glenn Clark,Jeffrey L. Dage,Gregory Scott Day,Ranjan Duara,Ani Eloyan,Tatiana Foroud,Neill R. Graff‐Radford,Ian M. Grant,Dustin B. Hammers,Lawrence S. Honig,Erik C. B. Johnson,David Thomas Jones
标识
DOI:10.64898/2026.01.25.26344738
摘要
Early-onset Alzheimer's disease (EOAD) and Late-onset AD (LOAD) differ in clinical presentations and rates of progression. We aimed to compare baseline and longitudinal tau PET burden, and their relationship with clinical variables in amyloid-PET positive, cognitively impaired participants from the Longitudinal Early-Onset Alzheimer's Disease Study (EOAD; n=390) and Alzheimer's Disease Neuroimaging Initiative (LOAD; n=211). Patients with EOAD showed higher baseline tau PET retention, broader neuroanatomical involvement and faster accumulation rates over time compared to LOAD, after adjusting for amyloid load and clinical stage. Tau PET showed stronger correlations with baseline amyloid burden and clinical measures of global cognition and function in EOAD than LOAD. We conclude that earlier age of onset in AD is linked to a more aggressive tauopathy, which in turn is a primary driver of clinical decline. These findings suggest that optimal therapeutic targets and strategies may differ between EOAD and LOAD.
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