18F‐Florzolotau PET Imaging Unveils Tau Pathology in Dementia with Lewy Bodies

路易氏体型失智症 神经病理学 路易体 正电子发射断层摄影术 病理 痴呆 颞叶 病态的 阿尔茨海默病 医学 体内 体素 神经科学 核医学 心理学 疾病 生物 放射科 生物技术 癫痫
作者
Gan Tang,Jiaying Lu,Xinyi Li,Rui‐Xin Yao,Yujie Yang,Fangyang Jiao,Mingjia Chen,Xiaoniu Liang,Zizhao Ju,Jingjie Ge,Yixin Zhao,Bo Shen,Ping Wu,Yi‐Min Sun,Jianjun Wu,Tzu‐Chen Yen,Chuantao Zuo,Jian Wang,Qianhua Zhao,Huiwei Zhang
出处
期刊:Movement Disorders [Wiley]
被引量:3
标识
DOI:10.1002/mds.30055
摘要

Abstract Background Dementia with Lewy bodies (DLB) commonly exhibits a complex neuropathology, sharing characteristics with Alzheimer's disease (AD), including tau aggregates. However, studies using the 18 F‐AV‐1451 tau tracer have shown inconsistent findings regarding both the extent and topographical distribution of tau pathology in DLB. Objectives Our aim was to elucidate the topographical patterns of tau deposition in DLB and to investigate the in vivo pathological distinction between DLB and AD in virtue of the 18 F‐Florzolotau positron emission tomography (PET) imaging. Methods This cross‐sectional study enrolled patients with DLB (n = 24), AD (n = 43), and cognitively healthy controls (n = 18). Clinical assessments and 18 F‐Florzolotau PET imaging were performed. 18 F‐Florzolotau binding was quantitatively assessed on PET images using standardized uptake value ratios and voxel‐wise analysis. Results 18 F‐Florzolotau PET imaging revealed widespread tau deposition across various cortical regions in DLB, uncovering heterogeneous topographical patterns. Among patients, 54.17% showed patterns similar to AD, whereas 16.67% exhibited distinct patterns. Compared to AD, DLB exhibited a unique in vivo neuropathological profile, characterized by a lower tau protein burden, heterogeneous topographical distributions, and a specific role of the medial temporal lobe in tau pathology. Conclusions 18 F‐Florzolotau PET imaging elucidated tau pathology patterns in DLB, providing valuable insights for future in vivo pathological differentiation and potential disease‐modifying therapies. © 2024 International Parkinson and Movement Disorder Society.
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