Tau-PET imaging predicts cognitive decline and brain atrophy progression in early Alzheimer’s disease

萎缩 认知功能衰退 匹兹堡化合物B 正电子发射断层摄影术 标准摄取值 神经科学 心理学 神经心理学 神经影像学 神经退行性变 认知 医学 淀粉样蛋白(真菌学) 病理 内科学 疾病 痴呆 认知障碍
作者
Julien Lagarde,Pauline Olivieri,Mattéo Tonietto,Cécile Tissot,Isabelle Rivals,Philippe Gervais,Fabien Caillé,Martin Moussion,Michel Bottlaender,Marie Sarazin
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:93 (5): 459-467 被引量:17
标识
DOI:10.1136/jnnp-2021-328623
摘要

To explore whether regional tau binding measured at baseline is associated with the rapidity of Alzheimer's disease (AD) progression over 2 years, as assessed by the decline in specified cognitive domains, and the progression of regional brain atrophy, in comparison with amyloid-positron emission tomography (PET), MRI and cerebrospinal fluid (CSF) biomarkers.Thirty-six patients with AD (positive CSF biomarkers and amyloid-PET) and 15 controls underwent a complete neuropsychological assessment, 3T brain MRI, [11C]-PiB and [18F]-flortaucipir PET imaging, and were monitored annually over 2 years, with a second brain MRI after 2 years. We used mixed effects models to explore the relations between tau-PET, amyloid-PET, CSF biomarkers and MRI at baseline and cognitive decline and the progression of brain atrophy over 2 years in patients with AD.Baseline tau-PET was strongly associated with the subsequent cognitive decline in regions that are usually associated with each cognitive domain. No significant relationship was observed between the cognitive decline and initial amyloid load, regional cortical atrophy or CSF biomarkers. Baseline tau tracer binding in the superior temporal gyrus was associated with subsequent atrophy in an inferomedial temporal volume of interest, as was the voxelwise tau tracer binding with subsequent cortical atrophy in the superior temporal, parietal and frontal association cortices.These results suggest that tau tracer binding is predictive of cognitive decline in AD in domain-specific brain areas, which provides important insights into the interaction between tau burden and neurodegeneration, and is of the utmost importance to develop new prognostic markers that will help improve the design of therapeutic trials.
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