MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1002/alz.14629

Медицинская библиотека · Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025

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

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

СтатьяПеревод в очереди

Аннотация

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.

Для цитирования: 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. Plasma Alzheimer's disease biomarker relationships with incident abnormal amyloid PET.. Alzheimer's & dementia : the journal of the Alzheimer's Association. 2025. DOI: 10.1002/alz.14629.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.