Yakoub Yara, Gonzalez-Ortiz Fernando, Ashton Nicholas J, Déry Christine, Strikwerda-Brown Cherie, St-Onge Frédéric, Ourry Valentin, Schöll Michael, Geddes Maiya R, Ducharme Simon, Montembeault Maxime, Rosa-Neto Pedro, Soucy Jean-Paul, Breitner John C S, Zetterberg Henrik, Blennow Kaj, Poirier Judes, Villeneuve Sylvia
Douglas Mental Health University Institute, Centre for Studies on the Prevention of Alzheimer's Disease (StoP-AD), Montreal, Quebec, Canada.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Alzheimers Dement. 2025 Feb;21(2):e14537. doi: 10.1002/alz.14537.
We assessed the prognostic accuracy of plasma p-tau217 in predicting the progression to mild cognitive impairment (MCI) in cognitively unimpaired (CU) individuals over a mean follow-up of 5.65 years after plasma collection (range 1.01-10.47).
We included 215 participants from the PREVENT-AD cohort with plasma Aβ and p-tau217, 159 with cerebrospinal fluid (CSF) Aβ and p-tau217, and 155 with F-NAV4694 and F-flortaucipir PET scans. MCI progression was determined by multidisciplinary consensus among memory experts blind to biomarker and genetic information.
Cox proportional hazard models indicated a greater progression rate in A+T+ and A-T+ compared to A-T- individuals (HR = 7.81 [95% CI = 3.92 to 15.59] and HR = 4.25 [1.60-11.31] respectively). Similar results were found with CSF (HR = 3.63 [1.72-7.70]) and PET (HR = 9.30 [3.67-23.55]).
Plasma p-tau217 is a prognostic marker for identifying individuals who will develop cognitive impairment within ten years.
Elevated plasma p-tau217 levels in CU individuals indicate future clinical progression. Adding plasma Aβ status to p-tau markers did not improve the prediction to MCI. All individuals with abnormal tau PET measured in a temporal meta-ROI progressed to MCI.
我们评估了血浆p-tau217在预测认知未受损(CU)个体进展为轻度认知障碍(MCI)方面的预后准确性,这些个体在血浆采集后平均随访5.65年(范围为1.01 - 10.47年)。
我们纳入了来自PREVENT-AD队列的215名参与者,他们有血浆Aβ和p-tau217检测数据,159名有脑脊液(CSF)Aβ和p-tau217检测数据,以及155名有F-NAV4694和F-氟代tau蛋白PET扫描数据。MCI进展由对生物标志物和基因信息不知情的记忆专家通过多学科共识确定。
Cox比例风险模型表明,与A-T-个体相比,A+T+和A-T+个体的进展率更高(HR分别为7.81 [95% CI = 3.92至15.59]和HR = 4.25 [1.60 - 11.31])。脑脊液(HR = 3.63 [1.72 - 7.70])和PET(HR = 9.30 [3.67 - 23.55])检测也得到了类似结果。
血浆p-tau217是一种预后标志物,用于识别将在十年内发生认知障碍的个体。
CU个体中血浆p-tau217水平升高表明未来的临床进展。将血浆Aβ状态添加到p-tau标志物中并不能改善对MCI的预测。在颞叶元感兴趣区测量的所有tau PET异常的个体均进展为MCI。