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Racial and ethnic differences in plasma biomarker eligibility for a preclinical Alzheimer's disease trial
Alzheimer's & Dementia ( IF 14.0 ) Pub Date : 2024-04-17 , DOI: 10.1002/alz.13803
Doris Patricia Molina‐Henry 1 , Rema Raman 1 , Andy Liu 1 , Oliver Langford 1 , Keith Johnson 2, 3 , Leona K. Shum 1 , Crystal M. Glover 4, 5, 6 , Shobha Dhadda 7 , Michael Irizarry 7 , Gustavo Jimenez‐Maggiora 1 , Joel B. Braunstein 8 , Kevin Yarasheski 8 , Venky Venkatesh 8 , Tim West 8 , Philip B. Verghese 8 , Robert A. Rissman 9 , Paul Aisen 1 , Joshua D. Grill 10 , Reisa A. Sperling 2, 3
Affiliation  

In trials of amyloid-lowering drugs for Alzheimer's disease (AD), differential eligibility may contribute to under-inclusion of racial and ethnic underrepresented groups. We examined plasma amyloid beta 42/40 and positron emission tomography (PET) amyloid eligibility for the ongoing AHEAD Study preclinical AD program (NCT04468659).

中文翻译:

临床前阿尔茨海默病试验血浆生物标志物资格的种族和民族差异

在针对阿尔茨海默病 (AD) 的降低淀粉样蛋白药物的试验中,不同的资格可能导致种族和族裔代表性不足的群体的纳入不足。我们检查了血浆淀粉样蛋白 β 42/40 和正电子发射断层扫描 (PET) 淀粉样蛋白是否符合正在进行的 AHEAD 研究临床前 AD 项目 (NCT04468659)。
更新日期:2024-04-17
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