Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals

被引:51
作者
Chhatwal, Jasmeer P. [1 ,2 ,3 ]
Schultz, Aaron P. [1 ,3 ]
Dang, Yifan [2 ]
Ostaszewski, Beth [2 ]
Liu, Lei [2 ]
Yang, Hyun-Sik [1 ,2 ,3 ]
Johnson, Keith A. [1 ,2 ,3 ]
Sperling, Reisa A. [1 ,2 ,3 ]
Selkoe, Dennis J. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
关键词
NEUROFILAMENT LIGHT-CHAIN; ALZHEIMERS-DISEASE; AMYLOID-BETA; DIAGNOSTIC PERFORMANCE; POTENTIAL BIOMARKER; CSF; DEMENTIA; BLOOD; RISK; PET;
D O I
10.1038/s41467-020-19543-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The availability of blood-based assays detecting Alzheimer's disease (AD) pathology should greatly accelerate AD therapeutic development and improve clinical care. This is especially true for markers that capture the risk of decline in pre-symptomatic stages of AD, as this would allow one to focus interventions on participants maximally at risk and at a stage prior to widespread synapse loss and neurodegeneration. Here we quantify plasma concentrations of an N-terminal fragment of tau (NT1) in a large, well-characterized cohort of clinically normal elderly who were followed longitudinally. Plasma NT1 levels at study entry (when all participants were unimpaired) were highly predictive of future cognitive decline, pathological tau accumulation, neurodegeneration, and transition to a diagnosis of MCI/AD. These predictive effects were particularly strong in participants with even modestly elevated brain beta-amyloid burden at study entry, suggesting plasma NT1 levels capture very early cognitive, pathologic and neurodegenerative changes along the AD trajectory.
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页数:10
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