Plasma Alzheimer's disease biomarker relationships with incident abnormal amyloid PET

IF 11.1 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's & Dementia Pub Date : 2025-02-24 DOI:10.1002/alz.14629
Petrice M. Cogswell, Heather J. Wiste, Stephen D. Weigand, Terry M. Therneau, Michael E. Griswold, Joel B. Braunstein, Tim West, Philip B. Verghese, Jonathan Graff-Radford, Alicia Algeciras-Schimnich, Val J. Lowe, Christopher G. Schwarz, Matthew L. Senjem, Jeffrey L. Gunter, David S. Knopman, Prashanthi Vemuri, Ronald C. Petersen, Clifford R. Jack Jr.
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Abstract

INTRODUCTION

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.

METHODS

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.

RESULTS

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.

DISCUSSION

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.

Highlights

  • 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.

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血浆阿尔茨海默病生物标志物与异常淀粉样蛋白PET的关系
应用血浆生物标志物预测异常淀粉样蛋白正电子发射断层扫描(PET)的数据有限。在这项研究中,我们评估了血浆阿尔茨海默病(AD)生物标志物与淀粉样蛋白PET初始阴性(A−)个体中淀粉样蛋白PET进展的关系。方法:我们纳入了290名认知未受损的梅奥诊所老年研究参与者。我们估计了每个基线血浆生物标志物与从A−到A+的进展以及淀粉样蛋白PET变化率的关联。结果淀粉样蛋白β 42/40、磷酸化tau217百分比(% P -tau217)和淀粉样蛋白概率评分2的四分位数差异分别为1.29 (P = 0.09)、1.38 (P <;从A−到A+进展的风险分别增加了0.001)和1.20 (P = 0.05),淀粉样蛋白PET年变化率分别增加了0.27 (P = 0.16)、0.50 (P = 0.007)和0.28 (P = 0.15)。在一级预防试验中,血浆%p-tau217可能是一种有用的筛选工具,用于对从正常到异常的淀粉样蛋白PET进展可能性增加的参与者进行富集。血浆磷酸化tau 217与淀粉样蛋白正电子发射断层扫描进展相关,从阴性到阳性。淀粉样蛋白β 42/40和淀粉样蛋白概率评分2的相关性较弱。年龄和载脂蛋白E ε4携带也是重要的预测因素。这些标记物可能有助于丰富初级预防试验。
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来源期刊
Alzheimer's & Dementia
Alzheimer's & Dementia 医学-临床神经学
CiteScore
14.50
自引率
5.00%
发文量
299
审稿时长
3 months
期刊介绍: Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.
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