Plasma tau/amyloid-β1-42 ratio predicts brain tau deposition and neurodegeneration in Alzheimer's disease

被引:135
作者
Park, Jong-Chan [1 ]
Han, Sun-Ho [1 ,2 ]
Yi, Dahyun [3 ]
Byun, Min Soo [3 ]
Lee, Jun Ho [4 ]
Jang, Sukjin [5 ]
Ko, Kang [6 ]
Jeon, So Yeon [4 ]
Lee, Yun-Sang [7 ]
Kim, Yu Kyeong [8 ]
Lee, Dong Young [3 ,4 ,9 ]
Mook-Jung, Inhee [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Biochem & Biomed Sci, Seoul 03080, South Korea
[2] Seoul Natl Univ, Coll Med, Neurosci Res Inst, Seoul 03080, South Korea
[3] Seoul Natl Univ, Inst Human Behav Med, Med Res Ctr, Seoul 03080, South Korea
[4] Seoul Natl Univ Hosp, Dept Neuropsychiat, Seoul 03080, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Med, Seoul 03080, South Korea
[6] Natl Ctr Mental Hlth, Dept Geriatr Psychiat, Seoul 03080, South Korea
[7] Seoul Natl Univ, Coll Med, Dept Nucl Med, Seoul 03080, South Korea
[8] SMG SNU Boramae Med Ctr, Dept Nucl Med, Seoul 07061, South Korea
[9] Seoul Natl Univ, Coll Med, Dept Psychiat, Seoul 03080, South Korea
基金
新加坡国家研究基金会;
关键词
blood biomarker; tau; F-18-AV-1451; tau-PET; Alzheimer's disease; MILD COGNITIVE IMPAIRMENT; FLUID TAU/BETA-AMYLOID(42) RATIO; CEREBROSPINAL-FLUID; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; T-TAU; BIOMARKERS; PET; PROTEIN;
D O I
10.1093/brain/awy347
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
One of the hallmarks of Alzheimer's disease is abnormal deposition of tau proteins in the brain. Although plasma tau has been proposed as a potential biomarker for Alzheimer's disease, a direct link to brain deposition of tau is limited. Here, we estimated the amount of in vivo tau deposition in the brain by PET imaging and measured plasma levels of total tau (t-tau), phosphorylated tau (p-tau, T181) and amyloid-beta(1-42). We found significant correlations of plasma p-tau, t-tau, p-tau/amyloid-beta(1-42), and t-tau/amyloid-beta(1-42) with brain tau deposition in cross-sectional and longitudinal manners. In particular, t-tau/amyloid-beta(1-42) in plasma was highly predictive of brain tau deposition, exhibiting 80% sensitivity and 91% specificity. Interestingly, the brain regions where plasma t-tau/amyloid-beta(1-42) correlated with brain tau were similar to the typical deposition sites of neurofibrillary tangles in Alzheimer's disease. Furthermore, the longitudinal changes in cerebral amyloid deposition, brain glucose metabolism, and hippocampal volume change were also highly associated with plasma t-tau/amyloid-beta(1-42). These results indicate that combination of plasma tau and amyloid-beta(1-42) levels might be potential biomarkers for predicting brain tau pathology and neurodegeneration.
引用
收藏
页码:771 / 786
页数:16
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