阿尔茨海默病
疾病
神经科学
磷酸化
选择(遗传算法)
工作流程
癌症研究
医学
临床试验
淀粉样β
生物信息学
药理学
扩展访问
计算生物学
退行性疾病
人血浆
血浆水平
临床前研究
体内
作者
Gemma Salvadó,Shorena Janelidze,Divya Bali,Anna Orduña Dolado,Joseph Therriault,Wagner S. Brum,Alexa Pichet Binette,Erik Stomrud,Niklas Mattsson,Sebastian Palmqvist,Emma M. Coomans,Charlotte E. Teunissen,Wiesje M. van der Flier,Nesrine Rahmouni,Tammie L.S. Benzinger,Juan Domingo Gispert,Kaj Blennow,Vincent Doré,Azadeh Feizpour,Christopher C. Rowe
出处
期刊:JAMA Neurology
[American Medical Association]
日期:2025-09-15
卷期号:82 (11): 1122-1122
被引量:15
标识
DOI:10.1001/jamaneurol.2025.3217
摘要
The findings highlight the potential of plasma p-tau217 as a stand-alone test-or when used in a sequential 2-step approach alongside PET or CSF testing-as a cost-effective, scalable, and minimally burdensome strategy for identifying preclinical AD. Tailored screening workflows that incorporate p-tau217 can improve efficiency in participant selection for preclinical AD trials and, in the future, help guide access to disease-modifying treatments.
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