Ossenkoppele Rik, Salvadó Gemma, Janelidze Shorena, Binette Alexa Pichet, Bali Divya, Karlsson Linda, Palmqvist Sebastian, Mattsson-Carlgren Niklas, Stomrud Erik, Therriault Joseph, Rahmouni Nesrine, Rosa-Neto Pedro, Coomans Emma M, van de Giessen Elsmarieke, van der Flier Wiesje M, Teunissen Charlotte E, Jonaitis Erin M, Johnson Sterling C, Villeneuve Sylvia, Benzinger Tammie L S, Schindler Suzanne E, Bateman Randall J, Doecke James D, Doré Vincent, Feizpour Azadeh, Masters Colin L, Rowe Christopher, Wiste Heather J, Petersen Ronald C, Jack Clifford R, Hansson Oskar
Clinical Memory Research Unit, Department of Clinical Sciences in Malmö, Lund University, Lund, Sweden.
Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Amsterdam, The Netherlands.
medRxiv. 2024 Jun 13:2024.06.12.24308824. doi: 10.1101/2024.06.12.24308824.
Plasma p-tau217 and Tau-PET are strong prognostic biomarkers in Alzheimer's disease (AD), but their relative performance in predicting future cognitive decline among cognitively unimpaired (CU) individuals is unclear. In this head-to-head comparison study including 9 cohorts and 1534 individuals, we found that plasma p-tau217 and medial temporal lobe Tau-PET signal showed similar associations with cognitive decline on a global cognitive composite test (R =0.32 vs R =0.32, p=0.812) and with progression to mild cognitive impairment (Hazard ratio[HR]=1.56[1.43-1.70] vs HR=1.63[1.50-1.77], p=0.627). Combined plasma and PET models were superior to the single biomarker models (R=0.36, p<0.01). Furthermore, sequential selection using plasma p-tau217 and then Tau-PET reduced the number of participants required for a clinical trial by 94%, compared to a 75% reduction when using plasma p-tau217 alone. We conclude that plasma p-tau217 and Tau-PET showed similar performance for predicting future cognitive decline in CU individuals, and their sequential use (i.e., plasma p-tau217 followed by Tau-PET in a subset with high plasma p-tau217) is useful for screening in clinical trials in preclinical AD.
血浆p-tau217和Tau-PET是阿尔茨海默病(AD)中强有力的预后生物标志物,但它们在预测认知未受损(CU)个体未来认知衰退方面的相对表现尚不清楚。在这项纳入9个队列和1534名个体的直接比较研究中,我们发现,在整体认知综合测试中,血浆p-tau217和内侧颞叶Tau-PET信号与认知衰退的关联相似(R = 0.32 vs R = 0.32,p = 0.812),与进展为轻度认知障碍的关联也相似(风险比[HR]=1.56[1.43 - 1.70] vs HR = 1.63[1.50 - 1.77],p = 0.627)。血浆和PET联合模型优于单一生物标志物模型(R = 0.36,p < 0.01)。此外,与单独使用血浆p-tau217时减少75%相比,先使用血浆p-tau217然后使用Tau-PET的序贯选择可将临床试验所需的参与者数量减少94%。我们得出结论,血浆p-tau217和Tau-PET在预测CU个体未来认知衰退方面表现相似,它们的序贯使用(即在血浆p-tau217高的亚组中先使用血浆p-tau217然后使用Tau-PET)有助于临床前AD临床试验的筛查。