神经完整成人囊状胆碱能转运蛋白变化的大脑地形:[18F]FEOBV PET研究

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2022-01-01 DOI:10.1016/j.nbas.2022.100039
Prabesh Kanel , Sygrid van der Zee , Carlos A. Sanchez-Catasus , Robert A. Koeppe , Peter J.H. Scott , Teus van Laar , Roger L. Albin , Nicolaas I. Bohnen
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引用次数: 11

摘要

乙酰胆碱在脑认知和运动功能中起重要作用,在一些神经退行性疾病中常见的区域性胆碱能终端丧失。我们使用正电子发射断层扫描(PET)配体[18F](-)5-氟乙氧基苯唑维氨醇([18F]FEOBV)描述了体内区域胆碱能神经元末端密度与年龄相关的下降,这是一种选择性结合囊泡乙酰胆碱转运体(VAChT)的维氨醇类似物。共有42例无神经系统疾病临床证据的受试者(平均50.55岁[范围20-80]岁,男24名/女18名)接受了[18F]FEOBV脑PET成像。我们使用基于SPM的体素统计分析来执行基于全脑体素的参数分析(family-wise error corrected, FWE),并提取与年龄相关的最显著的区域簇,将性别作为干扰变量。在初级感觉运动皮层、视觉皮层、尾状核、中扣带前部、双侧岛、海马旁、海马、前颞叶/杏仁核、丘脑背内侧、后丘脑和小脑中发现与年龄相关的VAChT结合减少(性别和fwe校正,P < 0.05)。这些发现表明,随着年龄的增长,胆碱能神经末梢在多个胆碱能系统中的区域易损具有特定的地形模式。
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Cerebral topography of vesicular cholinergic transporter changes in neurologically intact adults: A [18F]FEOBV PET study

Acetylcholine plays a major role in brain cognitive and motor functions with regional cholinergic terminal loss common in several neurodegenerative disorders. We describe age-related declines of regional cholinergic neuron terminal density in vivo using the positron emission tomography (PET) ligand [18F](–)5-Fluoroethoxybenzovesamicol ([18F]FEOBV), a vesamicol analogue selectively binding to the vesicular acetylcholine transporter (VAChT). A total of 42 subjects without clinical evidence of neurologic disease (mean 50.55 [range 20–80] years, 24 Male/18 Female) underwent [18F]FEOBV brain PET imaging. We used SPM based voxel-wise statistical analysis to perform whole brain voxel-based parametric analysis (family-wise error corrected, FWE) and to also extract the most significant clusters of regions correlating with aging with gender as nuisance variable. Age-related VAChT binding reductions were found in primary sensorimotor cortex, visual cortex, caudate nucleus, anterior to mid-cingulum, bilateral insula, para-hippocampus, hippocampus, anterior temporal lobes/amygdala, dorsomedial thalamus, metathalamus, and cerebellum (gender and FWE-corrected, P < 0.05). These findings show a specific topographic pattern of regional vulnerability of cholinergic nerve terminals across multiple cholinergic systems accompanying aging.

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Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
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