Cogswell Petrice M, Wiste Heather J, Weigand Stephen D, Therneau Terry M, Griswold Michael E, Braunstein Joel B, West Tim, Verghese Philip B, Graff-Radford Jonathan, Algeciras-Schimnich Alicia, Lowe Val J, Schwarz Christopher G, Senjem Matthew L, Gunter Jeffrey L, Knopman David S, Vemuri Prashanthi, Petersen Ronald C, Jack Clifford R
Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Alzheimers Dement. 2025 Feb;21(2):e14629. doi: 10.1002/alz.14629.
Limited data exist on the utility of plasma biomarkers to predict incident abnormal amyloid positron emission tomography (PET). In this study we evaluate the association of plasma Alzheimer's disease (AD) biomarkers with amyloid PET progression among initially amyloid PET negative (A-) individuals.
We included 290 A-, cognitively unimpaired Mayo Clinic Study of Aging participants. We estimated the association of each baseline plasma biomarker with progression from A- to A+ and with rate of amyloid PET change.
Interquartile range differences in amyloid beta 42/40, percent phosphorylated tau 217 (%p-tau217), and Amyloid Probability Score 2 were associated with 1.29 (P = 0.09), 1.38 (P < 0.001), and 1.20 (P = 0.05) increases, respectively, in the hazard of progression from A- to A+ and 0.27 (P = 0.16), 0.50 (P = 0.007), and 0.28 (P = 0.15) Centiloid/year increases, respectively, in annual rate of amyloid PET change.
Plasma %p-tau217 may be a useful screening tool to enrich for participants with increased likelihood of progressing from normal to abnormal amyloid PET in a primary prevention trial.
Plasma phosphorylated tau 217 was associated with amyloid positron emission tomography progression, negative to positive. The associations were weaker for amyloid beta 42/40 and Amyloid Probability Score 2. Age and apolipoprotein E ε4 carriership were also important predictors. These markers may be useful for enrichment of a primary prevention trial.
关于血浆生物标志物预测淀粉样蛋白正电子发射断层扫描(PET)异常事件发生的效用,现有数据有限。在本研究中,我们评估了最初淀粉样蛋白PET检查呈阴性(A-)的个体中血浆阿尔茨海默病(AD)生物标志物与淀粉样蛋白PET进展之间的关联。
我们纳入了290名认知功能未受损的梅奥诊所衰老研究参与者,他们最初的淀粉样蛋白PET检查呈阴性。我们估计了每个基线血浆生物标志物与从A-进展到A+以及淀粉样蛋白PET变化率之间的关联。
淀粉样蛋白β42/40的四分位数间距差异、磷酸化tau 217百分比(%p-tau217)以及淀粉样蛋白概率评分2分别与从A-进展到A+的风险增加1.29(P = 0.09)、1.38(P < 0.001)和1.20(P = 0.05)相关,以及与淀粉样蛋白PET每年变化率分别增加0.27(P = 0.16)、0.50(P = 0.007)和0.28(P = 0.15)Centiloid相关。
在一项一级预防试验中,血浆%p-tau217可能是一种有用的筛查工具,用于筛选出从正常淀粉样蛋白PET进展为异常的可能性增加的参与者。
血浆磷酸化tau 217与淀粉样蛋白正电子发射断层扫描从阴性到阳性的进展相关。淀粉样蛋白β42/40和淀粉样蛋白概率评分2的关联较弱。年龄和载脂蛋白E ε4携带者状态也是重要的预测因素。这些标志物可能有助于富集一级预防试验。