Amyloid Imaging with 18F-Florbetaben in Alzheimer Disease and Other Dementias

路易氏体型失智症 痴呆 额颞叶变性 医学 路易体 病理 疾病 认知障碍 阿尔茨海默病 内科学 心理学 失智症
作者
Victor L. Villemagne,Kevin Ong,Rachel Mulligan,Gerhard Holl,Svetlana Pejoska,Gareth Jones,Graeme O’Keefe,Uwe Ackerman,Henri Tochon‐Danguy,Janet Chan,Cornelia Reininger,Lueder Fels,Barbara Pütz,Beate Rohde,Colin L. Masters,Christopher C. Rowe
出处
期刊:The Journal of Nuclear Medicine [Society of Nuclear Medicine and Molecular Imaging]
卷期号:52 (8): 1210-1217 被引量:323
标识
DOI:10.2967/jnumed.111.089730
摘要

Amyloid imaging with (18)F-labeled radiotracers will allow widespread use, facilitating research, diagnosis, and therapeutic development for Alzheimer disease. The purpose of the study program was to compare cortical amyloid deposition using (18)F-florbetaben and PET in controls and subjects with mild cognitive impairment (MCI), frontotemporal lobar degeneration (FTLD), dementia with Lewy bodies (DLB), vascular dementia (VaD), Parkinson disease (PD), and Alzheimer disease (AD).One hundred nine subjects in 3 clinical studies at Austin Health were reviewed: 32 controls, 20 subjects with MCI, and 30 patients with AD, 11 with FTLD, 7 with DLB, 5 with PD, and 4 with VaD underwent PET after intravenous injection of 300 MBq of (18)F-florbetaben. Standardized uptake value ratios (SUVR) using the cerebellar cortex as a reference region were calculated between 90 and 110 min after injection.When compared with the other groups, AD patients demonstrated significantly higher SUVRs (P < 0.0001) in neocortical areas. Most AD patients (96%) and 60% of MCI subjects showed diffuse cortical (18)F-florbetaben retention. In contrast, only 9% of FTLD, 25% of VaD, 29% of DLB, and no PD patients and 16% of controls showed cortical binding. Although there was a correlation between Mini Mental State Examination and β-amyloid burden in the MCI group, no correlation was observed in controls, FTLD or AD.(18)F-florbetaben had high sensitivity for AD, clearly distinguished patients with FTLD from AD, and provided results comparable to those reported with (11)C-Pittsburgh Compound B in a variety of neurodegenerative diseases.
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