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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Cognitive reserve associated with FDG-PET in preclinical Alzheimer disease
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Cognitive reserve associated with FDG-PET in preclinical Alzheimer disease

机译:认知储备与正相关临床前阿尔茨海默病

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Objective: To examine the effect of education (a surrogate measure of cognitive reserve) on FDG-PET brain metabolism in elderly cognitively healthy (HC) subjects with preclinical Alzheimer disease (AD). Methods: Fifty-two HC subjects (mean age 75 years) with FDG-PET and CSF measurement of A1-42 were included from the prospective Alzheimer's Disease Neuroimaging Initiative biomarker study. HC subjects received a research classification of preclinical AD if CSF Ab1-42 was 192 pg/mL (A1-42 [+]) vs HC with normal Ab (A1-42 [-]). In regression analyses, we tested the interaction effect between education and CSF Ab1-42 status (A1-42 [+] vs A1-42 [-]) on FDG-PET metabolism in regions of interest (ROIs) (posterior cingulate, angular gyrus, inferior/middle temporal gyrus) and the whole brain (voxel-based). Results: An interaction between education and CSF A1-42 status was observed for FDG-PET in the posterior cingulate (p 0.001) and angular gyrus ROIs (p = 0.03), but was not significant for the inferior/middle temporal gyrus ROI (p = 0.06), controlled for age, sex, and global cognitive ability (Alzheimer's Disease Assessment Scale-cognitive subscale). The interaction effect was such that higher education was associated with lower FDG-PET in the Ab1-42 (+) group, but with higher FDG-PET in the A1-42 (-) group. Voxel-based analysis showed that this interaction effect was primarily restricted to temporo-parietal and ventral prefrontal brain areas. Conclusions: Higher education was associated with lower FDG-PET in preclinical AD (A1-42 [+]), suggesting that cognitive reserve had a compensatory function to sustain cognitive ability in presence of early AD pathology that alters FDG-PET metabolism. ? 2013 American Academy of Neurology.
机译:目的:研究教育(的效果代孕的认知储备)正子在老年认知脑代谢健康与临床前阿尔茨海默(HC)科目病(AD)。(平均年龄75岁)正与CSF测量的1-42是包括的未来的阿尔茨海默病神经影像倡议生物标志物研究。临床前研究分类广告CSF Ab1-42 & 192 pg / mL(1-42 [+])vs HC与正常Ab(1-42[-])。分析,我们测试了互动的效果教育和CSF Ab1-42之间地位(1-42[+] vs1-42正代谢[-])感兴趣的区域(roi)(后扣带,角形脑回,/中间颞下回)和整个大脑(分布)。互动教育和CSF1-42正的状态观察后扣带(p & (p = 0.03),但不显著/中间颞下回ROI (p = 0.06),控制了年龄,性别,和全球的认知(阿尔茨海默氏症评估能力Scale-cognitive次生氧化皮)。,高等教育有关吗Ab1-42较低的正(+)组,但是有较高的正1-42(-)组。分布分析表明,这种交互影响主要是受限制的大脑颞和腹侧前额叶区域。降低正子在临床前的广告(1-42[+]),这表明认知储备有一个补偿功能来维持认知能力在早期AD病理的存在改变正新陈代谢。神经学学院。

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