Teipel Stefan J, Drzezga Alexander, Bartenstein Peter, Möller Hans-Jürgen, Schwaiger Markus, Hampel Harald
Alzheimer Memorial Center, Department of Psychiatry, Ludwig-Maximilian University, Nussbaumstr. 7, 80336 Munich, Germany.
Psychopharmacology (Berl). 2006 Jul;187(1):86-94. doi: 10.1007/s00213-006-0408-1. Epub 2006 Jun 1.
Cholinergic enhancement is among the best established treatments of Alzheimer's disease (AD). The cognitive effects of treatment are thought to be mediated by improvement of neuronal transmission. Positron emission tomography using 18F-fluorodeoxyglucose (FDG-PET) by measuring cortical metabolic response to activation assesses integrity of neuronal transmission in vivo.
To determine the effects of treatment with donepezil, a centrally selective acetylcholinesterase inhibitor, on cortical metabolism in AD using 18FDG-PET.
We enrolled 23 patients, 18 of which completed the study, with mild to moderate probable AD (mini-mental status exam scores of 15-28, inclusive) in a double-blind cross over trial of 8 weeks donepezil compared to 8 weeks placebo with repeated double 18FDG-PET examinations during passive audio-visual stimulation. Effects of treatment on cortical metabolic response to stimulation were determined with a linear model on a voxel level using Statistical Parametric Mapping (SPM 99, Wellcome Department of Imaging Neuroscience, London).
Effects of treatment on cognitive measures were not different between donepezil and placebo. During passive audio-visual stimulation, patients showed activation in posterior visual and auditory areas and decreased activation in frontal cortex and basal ganglia. Resting state metabolism was increased with donepezil in left prefrontal cortex and decreased in right hippocampus. Cortical response to activation was increased in right hippocampus with donepezil compared to placebo.
Donepezil treatment shows a spatially limited functional effect on right hippocampus and left prefrontal cortical metabolism, independently of clinical response to treatment.
胆碱能增强是阿尔茨海默病(AD)最成熟的治疗方法之一。治疗的认知效果被认为是通过改善神经元传递来介导的。使用18F-氟脱氧葡萄糖的正电子发射断层扫描(FDG-PET)通过测量皮质对激活的代谢反应来评估体内神经元传递的完整性。
使用18FDG-PET确定多奈哌齐(一种中枢选择性乙酰胆碱酯酶抑制剂)治疗对AD患者皮质代谢的影响。
我们招募了23例患者,其中18例完成了研究,这些患者患有轻度至中度可能的AD(简易精神状态检查评分在15至28分之间,包括15分和28分),参加了一项双盲交叉试验,该试验将8周的多奈哌齐治疗与8周的安慰剂治疗进行比较,在被动视听刺激期间进行重复的双次18FDG-PET检查。使用统计参数映射(SPM 99,伦敦惠康影像神经科学部)在体素水平上通过线性模型确定治疗对皮质刺激代谢反应的影响。
多奈哌齐和安慰剂在治疗对认知指标的影响方面没有差异。在被动视听刺激期间,患者在后部视觉和听觉区域表现出激活,而在额叶皮质和基底神经节的激活减少。多奈哌齐使左侧前额叶皮质的静息态代谢增加,右侧海马体的静息态代谢减少。与安慰剂相比,多奈哌齐使右侧海马体对激活的皮质反应增加。
多奈哌齐治疗对右侧海马体和左侧前额叶皮质代谢显示出空间有限的功能影响,与治疗的临床反应无关。