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A new method to quantify tau pathologies with 11C-PBB3 PET using reference tissue voxels extracted from brain cortical gray matter

机译:一种使用11C-PBB3 PET定量tau病理的新方法该方法使用从大脑皮层灰质中提取的参考组织体素

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摘要

BackgroundQuantitative in vivo imaging of tau pathologies potentially improves diagnostic accuracy of neurodegenerative tauopathies and would facilitate evaluation of disease-modifying drugs targeting tau lesions in these diseases. Tau pathology can be quantified by reference tissue models without arterial blood sampling when reference tissue devoid of target binding sites is available. The cerebellar cortex has been used as a reference region in analyses of tau positron emission tomography (PET) data in Alzheimer’s disease (AD). However, in a significant subset of tauopathies such as progressive supranuclear palsy and corticobasal degeneration, tau accumulation may occur in diverse brain regions including the cerebellar cortex. This hampers selection of a distinctive reference region lacking binding sites for a tau PET ligand. The purpose of this study was to develop a new method to quantify specific binding of a PET radioligand, 11C-PBB3, to tau deposits using reference voxels extracted from cortical gray matter, which have a low likelihood of containing tau accumulations.
机译:背景技术tau病理学的定量体内成像可能会改善神经退行性tauo病的诊断准确性,并将有助于评估针对这些疾病中tau病变的疾病修饰药物。当没有靶结合位点的参考组织可用时,Tau病理学可以通过参考组织模型进行定量,而无需动脉血取样。小脑皮层已用作阿尔茨海默氏病(AD)的tau正电子发射断层扫描(PET)数据分析的参考区域。然而,在诸如继发性核上性麻痹和皮质基底神经退行性变之类的tauopathies的重要子集中,tau积累可能发生在包括小脑皮质在内的各种大脑区域中。这阻碍了对缺乏针对tau PET配体结合位点的参考区域的选择。这项研究的目的是开发一种新方法,使用从皮质灰质中提取的参考体素来量化PET放射性配体 11 C-PBB3与tau沉积物的特异性结合。包含tau堆积物。

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